Israel as an independent sovereign nation was registered as a corporation in 1947 when the state of Israel was created. The registration expired on October 31, 2023. A corporation cannot register itself twice under the same name particularly if it is bankrupt.
Once a corporation is formed it exists as a separate entity from its owners meaning it has its own name, tax ID number, legal rights and obligations as a corporate structure. Israel is bankrupt and when it enters that status it has zero contract rights.
It means that if Israel was involved in human trafficking its assets are frozen.
Israeli Parliament forms emergency government on October 11 to deal with the Hamas incursion
The government has also established a paramilitary National Guard independent of the police and under the direct control of the Minister of National Security Itamar Ben-Gvir, while governing powers in the West Bank have been handed to a civilian for the first time in Minister Bezalel Smotrich in what has been labelled a de jure annexation. These two ministers are prominent examples of the far-right allies brought into government for the first time by Netanyahu after the November 2022 election.
The prominent ones are pretty lame. I’m less prominent and you’ll lose.
I bet you $100 million that the Ribonuclease enzyme destroyed (compared to the COVID antibody) more COVID mRNA within human lung cells in 2020.
since we’re talking animals? apparently, there’s no point debating with a chicken since they’re so PFIZER CHICKEN.
whether you debate me or NOT, just having ME, the guy with the BEST papertrail on EARTH to show that FAUCI should be in prison, JUST having ME engage with you? spells BAD NEWS FOR YOU.
I first informed FAUCI of the stupidity of the COVID vaccine hypothesis of a neutralizing antibody that had no path into the lung air space in Oct 2020. HE responsed via Dr. Erbelding in Nov 2020. I responded with a 73 pg letter FEB 2021, with a US copyright.
Hasan? interested in TRUTH? or PROMOTING your COVID vaccine?
Okay, let me spell out what happens NOW, since you’ve been informed of the FATAL flaw with the COVID VACCINE. if YOU continue to PROMOTE THIS SHIT SHOT? you have a HIGH chance of being sued by someone who actually gets the dumb shit shot based on YOUR PROMOTION of it.
ah, you think you have LEGAL IMMUNITY? that shit is NO GOOD if there is WILLFUL MISCONDUCT on your part based on the PREP act. look it up. So, if you CONTINUE to promote the vax in SPITE of being informed, don’t YOU think the jury will conclude “willful misconduct”??
so shut up about your stupid covid vaccine. admit you’re a chicken. you know i did this one sided debate with sam harris. two days later he blocked me. 4 days later he deleted his twitter account. pay attention.
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA Will they care about their reputations? and that parents KNOW that they got irrefutable information that makes them look EVIL? Yeah, I’ve been fighting this EVIL for almost 4 years. So, I’m only ACTING surprised. What I’m really doing?
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA what I’m really doing? just for the sake of a little justice in this world, I’m leaving as many papertrails as I can to all the EVIL men and women who will commit atrocities like this for their gain. and the others who just watch as the atrocities are committed.
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA have I given up that scientific leaders and dumb attorney leaders will do the right thing? yeah. but, if there is any humanity left in any of them, i want them to KNOW exactly what it is they are doing, so they can’t live with their guilt. or at least they always have to wonder
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA if there is a higher being watching. if karma really does exist. i don’t want them to live with an easy rationalization (it was scientific and science based). I want them to KNOW that they are vaccinating children, in just the same way that —
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA the high priests of human child sacrifice killed children. no, of course they didn’t kill ALL the children. just a few. and the pediatricians of today? all 67,000? are doing the same thing. and just like those priests of old? can they EVER believe that they were actually —
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA can they EVER believe that they were THAT EVIL? No, they convinced themselves that they were doing GOOD. Yes, even THOSE high priests of human child sacrifice could think that. and is their DNA much different from the DNA of pediatricians? a 100% match. so, I want the 67,000-
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA i want the 67,000 strong pediatricians (not strong compared to me. intellectually infantile, ONLY strong compared to the children they give Kool aid too) to have to have NIGHTMARES of what they’ve done and continue to do.
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA I want them to be afraid to sleep because every time they shut their eyes, rotting children with their huge dead eyes are always following them. harmless really. but they follow nonetheless, they follow all the pediatricians and keep asking. ” i want to get better–
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA — can you give me those three shots again, each a combo you said? what’s a combo? I want the 3 combos. it hurts. but i trust you. I know i’ll be better if i get those three magical combos.” and the nightmares will never stop. they will drink themselves to death.
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA their marriages will fall apart. becuz the spouse knows. yes, he/she/them/their/assholes knows that you’re stressed and short because another child seems “afflicted” only 2 weeks after their magical combos.
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA i want these priests/pediatricians to have their children look up at them. and you’ll never know. how much your own children know. do they know? what you did? that you killed children to put food on the table for THEM? then why does it seem your OWN kids are —
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA why does it seeem.. that your OWN kids are JUDGING YOU. and then, they never come by. you’re old now. you’re grey. you soil yourselves all the time. and you have no one. you want to confess. but there is on one to confess to. there is no forgiveness for your soul.
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA because, when you read my Antibody String Mechanism, you are shaken to the core. you suspected but always just thought about something else. but you NEVER got to the point of REALLY questioning the vaccines. You just . . . kept busy and silenced the questioning.
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA and now? you’ve actually read the Antibody String Mechanism. and it doesn’t leave you any room to say, “but this, or but that.” So, now you know. you really did kill those children. you thought you were helping, you really did. but they died.
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA and you were at peace with believing that you REALLY were doing it for the children, even though ANY time you worried whether vaccines were good or not, you silenced that little inner voice. but now? there is no rationalization available for u. you’re a killer.
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA and damn. your children will read this. and they’ll wonder why you didn’t think of it. how can you tell them? I didn’t WANT to figure it out. I COULD have. as you can see, it’s really simple, the string thing. now, to your kids, you’re dumb. but i’m not.
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA I could have EASILY figured it out, if some eye doc figured it out and drew the diagram on half a page. not even that. but. i can’t tell my children i decided to silence that inner voice. that makes me sound bad. i AM bad.
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA and now? everyone knows. i’m either really dumb. or i’m really evil and silenced my brain that wanted to ask questions about the vaccine. so, no one wants to talk to and see a dumb doctor. no one wants to talk and see an EVIL doctor. what am i. is THIS what they mean?
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA when they say “good will overcome?” this is it? i’m evil and now no one wants to have anything to do with me? not even the pedophiles? yes, not even the pedophiles want to be near u. they love children in the wrong way. but they don’t KILL children. (this is all fiction)
@TivnTivn @SecBecerra @AmerAcadPeds @MedBoardOfCA NOT. This is my prediction for the future. i’m good at that. because I know how to use science well. and the whole point of science? to be able to predict the future a bit better than the next guy. in my case? a HELLUVA lot better than the child killers.
1.1 The mRNA technology may be compared to a MONKEY throwing a WRENCH into a finely tuned WARP DRIVE. OR. A hypothesis for how the COVID mRNA vaccine may cause CANCER
1.2 Please remember. this is a HYPOTHESIS. which IS how science starts. and JUST ONE hypothesis. there may be THOUSANDS but of course with the CAMPAIGN against MISINFORMATION, scientists probably haven’t asked ANY questions that threw SHADE on the mRNA vaccine.
1.3 Let’s imagine that the COVID mRNA vaccine is injected into a patient (we don’t have to imagine really, it was injected, what 10 billion times?).
The mRNA is synthetic. It is also made of N1-Methylpseudouridine which INCREASES translation.
1.4 Basically, this N1-Methylpseudouridine incorporation into mRNA means that MORE proteins are made with mRNA that has this within the mRNA.
So, this COVID synthetic mRNA is injected into a patient. The LNP goes INTO say a MACROPHAGE.
1.5 The MACROPHAGE over time DEGRADES the synthetic mRNA. Now, this N1-Methylpseudouridine can be incorporated into OTHER normal mRNA that the macrophage makes. Let’s say a bunch of this N1-M is incorporated into an mRNA for a GROWTH factor.
1.6 This macrophage now has an mRNA for a GROWTH factor that has INCORPORATED synthetic N1-M’s into it so MORE GROWTH FACTOR PROTEIN IS MADE.
1.7 The surrounding cells grow SO FAST that now this poor MACROPHAGE doesn’t have enough BLOOD SUPPLY and feels hungry and naturally the response is to produce MORE ENDOTHELIAL CELL GROWTH FACTOR to provide BLOOD VESSELS FOR OXYGEN.
1.8. The MACROPHAGE is STARVED for oxygen and nutrients and has synthetic mRNA for producing GROWTH factors like MAD and keeps pumping out MORE AND MORE GROWTH FACTORS.
1.9 Remember. mRNA is unusual. it is like PAPER. the 4 subunits of mRNA are degraded and RE-used OVER and OVER again in this MACROPHAGE. So, EACH time mRNA for growth factors are made, LOTS MORE GROWTH FACTORS are produced.
2.0 As this “TUMOR” grows, the lack of oxygen and nutrients to the center of this haphazard bizarre growth, CONTINUES to provide a signal to the MACROPHAGE to CONTINUALLY PUMP out GROWTH FACTORS and now it’s a SELF SUSTAINING NIGHTMARE MESS.
2.1 Let’s say this NIGHTMARE started with a clump of a 1000 macrophages? then, as this MASS breaks up, any small CLUMP that breaks off and spreads, if it has a MACROPHAGE in that clump, there will STILL be an inadequate oxygen flow to that MACROPHAGE
2.2 That is what is known in “cancer” terminology as a METASTASIS. What I call “CLUMPS” with a macrophage at the center that has this SYNTHETIC mRNA that the macrophage DOES NOT POOP OUT but CONTINUES to recycle. a 1000 clumps? that continue to SPREAD and grow?
2.3 Surgeons will just GIVE UP not knowing that when they remove a 1000 metastasis the process will stop. yeah right. who will EVER try to remove a 1000 growing clumps? what insurance will EVER pay for THAT?
2.4 It IS a hypothesis. It’s just ONE. I can imagine MANY MANY MORE. so, NO. you can NOT tell me this synthetic mRNA is SAFE. if you do NOT allow DIALOGUE and DISCUSSION and DEBATE and TRANSPARENCY in your FUCKED UP SCIENCE. YOU PIECES OF SHIT, the DEM LEADERSHIP —
2.5 That THOUGHT that CENSORSHIP would HELP THE GROUP, that you were SOOO SURE that you were CORRECT that you needed NO DISCUSSION and believed it was CORRECT to SILENCE the OPPOSING VIEW. YOU DEMS WILL BE HELD TO ACCOUNT.
@RFKJR_4_POTUS I have had a lot of negative things to say about you because of the COVID vaccine. But I’m giving you another chance because you used consultants who gave you very bad advice.
Look at what I’ve found.
I have 300+ posts on the @AmerAcadPeds and NOT–
@RFKJR_4_POTUS @AmerAcadPeds NOT FAVORABLE to the AAPeds but they dare not BLOCK me or DELETE these tweets that have life-saving information.
This ANTIBODY STRING MECHANISM will take down half the vaccines on earth. The AAPeds is HIGHLY STRESSED. This is the time RFKjr. This is the time to JOIN THIS.
@RFKJR_4_POTUS @AmerAcadPeds I appreciate you following me back and what I think of you and what I say about you will matter at some point. I am giving you a break because your consultant doctors, McCullough, Malone and Kory (nasty nass) gave you HORRIBLE advice. But, now? ANYONE can understand THIS.
@RFKJR_4_POTUS @AmerAcadPeds RFK, with the utmost respect, we know you’ve done a TON for children’s health. I believe you made a mistake when you got my info from your lawyer and then decided not to use my papertrail. But, that’s not nearly as big a mistake as your physician consultants made.
@RFKJR_4_POTUS @AmerAcadPeds I will never re-interpret what McCullough and Malone and Kory and Nass did. I have formed my opinions about them. But you? If your heart is in the right place and you are anti-vax, this ONE DIAGRAM, will end half the vaccines on earth. You can be a part of it, or not.
@RFKJR_4_POTUS @AmerAcadPeds I have sent a 156 pages explaining this to the CHIEF EDITOR at the Journal of Immunology. He was UNABLE to provide a scientific rebuttal for 7 days and then made the DUMB MOVE to BLOCK me which will be evident for the world to judge becuz I published the thread on my SUBSTACK
@RFKJR_4_POTUS @AmerAcadPeds RFKjr, this is the time. I have set the stage. I can’t do much more with my limited reach. But, you can do what all your followers want you to do. Help END vaccines for children. All you have to do? You don’t even have to commit to this STRING MECHANISM.
@RFKJR_4_POTUS @AmerAcadPeds You JUST have to ask the AAPeds to provide a SCIENTIFIC REBUTTAL with a SIGNATURE with an opportunity for me to respond. The world will know that the AAPeds can’t respond. Then, the ONLY other option is for the AAPeds to call for a HALT to HALF the vaccines on EARTH.
@RFKJR_4_POTUS @AmerAcadPeds RFKjr. You are the chosen one for this. No one has as much influence or clout in the anti vax world. But, your decision here will CEMENT even your followers belief about you. Are you REALLY ANTI-VAX??
@RFKJR_4_POTUS @AmerAcadPeds If you get opinions from your physician consultants, demand it in writing with signatures. Because if they are negative about this ANTIBODY STRING MECHANISM, when EVEN the AAPeds can’t formulate a response, you will KNOW that your consultants are not qualified.
@RFKJR_4_POTUS @AmerAcadPeds AND, what do you have to lose? All I am asking you to do? is PUBLICLY ask the AAPeds to provide a SCIENTIFIC REBUTTAL to this CLEARLY NIGHTMARISH INFORMATION for children WITH a signature. and a chance for me to respond. We ARE all here? because we ALL want the best 4 KIDS?
@RFKJR_4_POTUS @AmerAcadPeds don’t you think RFK would respond to a thread like this? can you forward to him?
Ready to have your tiny minds blown? @jjcouey x @lasikeyecenter1 Dr. Joe Lee breaks down the issue with the vaxxes but it's amazing to watch Couey come to the same conclusion in real-time pic.twitter.com/7yAGwNjnAW
@harvardmed aren’t you guys supposed to be the BEST and BRIGHTEST? THIS is a REAL LIFE PARADIGM SHIFT in FRONT OF YOUR VERY EYES!!!!!!!
My thoughts? NO ONE should be able to be called an M.D. if they can’t explain this SIMPLE ONE DIAGRAM.
@harvardmed Okay, if HARVARD med students are FROZEN INTO SILENCE because this SIMPLE DIAGRAM is TOO hard for their minds to grasp, let me take it to Univ of Michigan, MY alma mater and see if this is just as issue for ALL med students these days, woke and not very bright.
Thank you for your recent email directed to Dr. Francis Collins, Director of the National Institutes of Health (NIH); Dr. Lawrence Tabak, Principal Deputy Director of the NIH; Dr. Anthony S. Fauci, Director of the National Institute of Allergy and Infectious Diseases (NIAID), NIH; Dr. Gary Gibbons, Director of the National Heart, Lung, and Blood Institute, NIH; and Dr. Amy Wernimont in the NIH Center for Scientific Review regarding vaccine-induced immune responses to respiratory infections, particularly severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and the disease it causes, coronavirus disease 2019 (COVID-19). Your message was forwarded to NIAID for response. NIAID is the NIH Institute with primary responsibility for research on infectious, immunologic, and allergic diseases. As the Director of the NIAID Division of Microbiology and Infectious Diseases, I am pleased to respond.
Patients infected with SARS-CoV-2 may present with a range of symptoms of varying severity, from fever and shortness of breath to pneumonia and acute respiratory distress syndrome. Symptom presentation is indicative of the region of the lungs infected by SARS-CoV-2, with infection of the lower respiratory tract causing moderate to severe disease outcomes.
Preclinical animal studies of SARS-CoV-2 candidate vaccines have evaluated viral titers and the level of neutralizing antibodies in bronchoalveolar lavage (BAL) fluid collected from the lower respiratory tract. Investigators found evidence of reduced viral replication and an increase in antibodies to the antigen in the candidate vaccine in BAL fluid [1, 2, 3, 4] (antibodies from blood plasma cross the blood-air interface and enter the BAL fluid through a process called transudation; secretion from the airway tissues and the immune response localized in the lung also play a role [5]). Further, preclinical animal studies have also shown that SARS-CoV-2 candidate vaccines control SARS-CoV-2 infection in the airways as well as prevent pneumonia [1, 2, 3, 4].
Building on the preclinical animal studies, evaluation of SARS-CoV-2 candidate vaccines in Phase 1 and 2 clinical trials have shown that the candidate vaccines induce neutralizing antibody responses and cell mediated responses (T cell responses); further analysis of these immune responses is ongoing [6, 7, 8, 9, 10, 11]. The induction of antibody and cell mediated responses is indicative of a multifaceted immune response, which is important in protecting against disease. Currently, several SARS-CoV-2 candidate vaccines are being evaluated in large Phase 3 clinical trials to determine the effectiveness of a candidate vaccine in protecting against symptomatic COVID-19 disease. The results of these trials will determine whether one or more SARS-CoV-2 vaccines may be administered at the population level. Guidance from the U.S. Food and Drug Administration has indicated that prevention of severe disease due to SARS-CoV-2 will be one standard for vaccine approval, along with safety considerations (https://www.fda.gov/regulatory-information/search-fda-guidance-documents/emergency-use-authorization-vaccines-prevent-covid-19).
In addition, monoclonal antibodies have also been shown to reduce COVID-19 disease and enhance recovery. Data from pre-clinical, as well as clinical trials, have demonstrated anti-viral effects of these neutralizing antibodies directed at the spike protein with important clinical benefits [12, 13, 14, 15]. This is precisely the type of immune response the vaccines are designed to elicit.
Further, the effectiveness of immunizations against influenza, Bordetella pertussis, Streptococcus pneumoniae, Haemophilus influenzae type b, measles, and tuberculosis, demonstrates the utility of vaccines in combating respiratory infections. Moreover, monoclonal antibodies against respiratory syncytial virus are used to prevent serious disease in the lower respiratory tract of recipients.
We appreciate the opportunity to describe the results of some studies regarding the development of vaccines and monoclonal antibodies to combat COVID-19, and hope you find this information useful.
what worked when you got COVID? your body. that’s the MAIN thing that worked. Not the powders, not the drugs, not the herbs, not the vitamins, the sunlight, any other thing. YOUR BODY. And understanding? what your body actually did? to STOP the virus from growing? —
the SAME main mechanism OUR body uses to SLOW DOWN OUR cells from growing when we don’t eat, destroy our OWN RNA with Ribonuclease enzymes. and these RNase enzymes are NOT specific to OUR RNA but ALSO destroy VIRAL RNA. So, once you understand HOW the body is controlling —
Once, you understand HOW the body is controlling the virus? via RNase enyzmes. THEN, and ONLY THEN can you TRULY help the body do what it is doing AMAZINGLY well. and my fortuitous discovery was that FASTING activates this RNase EVEN more. —
–and some say, it is MUCH to simple. I say, 70% of a dry weight of a CELL is PROTEIN. Preventing PROTEIN production DOES prevent OUR cell growth. Destroying OUR RNA DOES Prevent protein production, which DOES prevent cell growth. What a beautiful system!
IF all OUR cells were STILL trying to HOARD glucose when supplies were LOW and STILL trying to GROW when we aren’t eating, THOSE ARE CANCEROUS CELLS. It is INCREDIBLE that EACH and EVERY cell in our body KNOWS to control its GROWTH when we fast.
and this SAME system of CONTROLLING OUR cell growth by REMOVING the TEMPLATES for ALL PROTEIN (mRNA is the template) via Ribonuclease/endonuclease enzymes is ACTUALLY the SAME system that helps us control VIRAL GROWTH.
and the proof? that THIS system IS the main ACTIVE one that our body uses in the EARLY fight against viruses? (before chemokines/interferon ramp up). Evolution has TIME on its hands. And USUALLY gets it right. Do you see us always trying to get SUNLIGHT when we are sick? —
do you see us ALWAYS wanting to eat FRUIT and get Vitamin C when we are sick? no. Do you see us hunting down zinc rich dirt to eat when we are sick? no. I’m NOT saying these things are NOT important. but, what is the MAIN thing we try to do? behaviorally?
uniformly, the MOST consistent thing ALL humans do is have a desire to NOT EAT. If you have kids, you KNOW this is true. if you’re a HUMAN, you KNOW this is true. but, some people insist on PEER REVIEWED PAPERS before they believe anything. look at ALL the peer reviewed —
papers that got it ALL wrong. I can guarantee you. There will be MANY clinical trials on the efficacy of FASTING versus EATING for respiratory viral illnesses. EVERY ONE OF THEM will have to be STOPPED EARLY because it will be UNETHICAL to NOT offer FASTING to the CONTROL ARM.
Chair, Department of Microbial Infection and Immunity Samuel Saslaw Professor of Infectious Diseases, Microbial Infection and Immunity
776A Biomedical Research Tower (BRT) 460 W 12th Ave, Columbus OH 43210 Eugene.Oltz@osumc.edu 614-293-7570
Dear Dr. Eugene Oltz,
I also called and left a message.
This is the preface to the 156 page letter attached here. The most important section is the “Lee String ” Mechanism. This String mechanism will end half the vaccines on earth this year. This is a matter of utmost importance for protecting American lives and protecting our children.
It is the simplest mechanism. When you are infected with a COVID virus, since the Spike antigen is attached to the virus particle, you do not form antibodies against the bottom of the spike antigen, you DO form antibodies to the top of the spike antigen.
In a vaccine setting, you have free spike antigen in the blood and lymph and you will form antibodies to the TOP of the spike and ALSO to the BOTTOM of the spike antigen. There is no dispute that there are MULTIPLE antigenic sites on the Spike antigen.
Prior to receiving a booster vaccine, we all agree that, without a doubt, these three components are in the blood.
COVID antibodies to the top of the spike antigen are present.
COVID antibodies to the bottom of the spike antigen are present.
Once, the booster is given, spike antigen is added to the above two antibodies. Following a booster COVID mRNA vaccine given within a few months of the first COVID mRNA vaccine, there will be present in the blood at the same time; COVID antibodies to the top of the spike antigen, COVID antibodies to the bottom of the spike antigen, and spike antigen. No vaccine scientist on earth can dispute these three points.
Referring to FIG. 1, the booster vaccine results in the body producing spike antigen that is now present in the blood/lymph. One arm of an IgG (Top) binds to the top of the spike antigen (1). One arm of an IgG (Bottom) binds to the bottom of the same spike antigen (1). The second arm of an IgG (Bottom) binds to another spike antigen (2). One arm of a second IgG (Top) binds to the same spike antigen (2). The second arm of the second IgG (Top) binds to a third spike antigen (3). And the pattern can continue indefinitely, producing thick strands of antibody/antigen complexes. There can be many separate “strings” of alternating IgG (Top) and IgG (Bottom) antibodies. Can you see how this meshwork of strings is the basis for long gelatinous, clots? The chances of this occurring with a real COVID virus infection is very low because the virus particle is too large to act as “glue” between alternating antibodies.
There can be infinite variations of the resulting meshwork patterns and size that can emerge from strings of antibodies formed from the mix of IgG antibodies and IgM antibodies and the spike antigen that act as glue connecting 1) antibodies both IgG and IgM to the top of the spike antigen and 2) antibodies both IgG and IgM to the bottom/side of the spike antigen. The strands of antibodies can be of variable length and some strands may form into balls not that different from balls of string. It is not inconceivable that some of these “balls” of antibodies grow large enough to block blood vessels, with all the downstream damage from blocked blood flow.
Lattice structures formed from immune complexes (antibodies binding to their respective antigen) are a well-known phenomenon and have been extensively studied. Lattice structure formation is affected by many factors. With the COVID spike antigen, we have an extremely unusual situation that dramatically increases the size and length of these structures. With a natural COVID viral infection, antibodies are only formed to the top of the spike antigen. However, free spike antigen generated following the COVID mRNA vaccine results in the production of at least two distinct antibodies, to the top and bottom of the spike antigen. This creates a bizarre situation following administration of the booster COVID mRNA vaccine. There are antibodies now present to the top of the spike antigen and to the bottom (or stalk portion) of the spike antigen.
This opens the possibility for a never-ending weave of lattice structures or strings, until the respective antibodies and spike antigen becomes unavailable due to the formation of extensive lattice structures (and strings of variable length) which create extended clots. The chances of a COVID antibody molecule formed in response to the first COVID vaccine binding a natural COVID virus is at least a million times less than the chances of that same COVID antibody molecule combining with a spike antigen and being found within a meshwork of antibodies. That is why I call this the “Lee string theory that is more fact than theory.” This is why the resulting meshwork of antibodies is the “MAIN EFFECT” of the booster COVID mRNA vaccine. If a side effect of the COVID mRNA vaccine occurred as infrequently as the chance of their COVID antibody binding a COVID virus in the lung, the vaccine scientists would not even list it as a “side effect.” Again, this is exactly why I state that this string formation of antibodies IS THE MAIN EFFECT of the COVID mRNA vaccine.
It is well known that immune complex clearance is affected by the size of the lattice structure. Because of the unusual situation with the free spike antigen resulting in production of at least two different antibodies, immune complexes can criss-cross and form alternating connections with other immune complexes, in ways that would be extremely unlikely if only antibodies to the top of the spike antigen are present. The larger the meshwork of antibodies with spike antigen as the glue connecting the various antibodies, the more unlikely that the normal clearance mechanism can be effective.
The chances of a “double immune complex” forming is much less because if a TOP antibody has two spike antigens bound, one to each arm, for the BOTTOM antibodies two arms to reach the bottom of each spike antigen, the binding would be limited by the angle that the arm projects out, since the body of the antibody would have to be parallel in at least one view, to the TOP antibody.
Similar to how pine needles and leaves can clog gutters and prevent water flow, strings of antibodies, platelets, white blood cells, red blood cells, and coagulation activation can create blockage of blood vessels all over the body. All you have to do is imagine how your shower drain can be blocked by strands of hair and gunk.
This mechanism ONLY uses facts that are so widely acknowledged that the COVID mRNA vaccine should be immediately HALTED. For example, I have a theory that if I throw a banana off the roof of my house, it will fall to the ground. I have NEVER studied this. I have done NO research trials on this theory. Yet, I am certain that the banana will fall. In exactly the same way, the chances of an antibody to the spike from the first vaccine actually binding to a real COVID virus is less than 1 in a 1000, probably less than 1 in a million. But the chances of that same antibody from the first vaccine binding to a spike antigen from the second vaccine is almost guaranteed. Strands/chains of alternating antibodies are definitely being formed. How large that meshwork is will vary from patient to patient. At a certain critical threshold of meshwork size, clots will form. Again, strand formation is NOT a side effect. It is in fact the “MAIN EFFECT” of the vaccine to produce an antibody that WILL bind to the spike antigen from the second vaccine.
Without being informed of this breaking new information, it is not possible for a single physician on earth to provide proper informed consent to a prospective COVID vaccine patient. It is NOT my responsibility to perform the additional research to vet this issue; it is the undisputed obligation of the manufacturers of the vaccine (those who make the profit). They listed “clots” as a “side effect” in their warning labels. If the “side effect” of strand formation occurs much more frequently than the “main effect” of the antibody binding to a COVID virus, shouldn’t they be required to UPDATE their warning labels AND report this breaking information to the FDA?
Children in the US receive up to 20 boosters before the age of 4. Half of these booster use vaccines with antigens that can act as glue. Then, under the age of 4, children are exposed to booster vaccines 10 times that can drastically increase their likelihood of clots. A clot in a capillary in brain tissue can cause a personality change, or autism. The potential risk of autism is not from a strange ingredient in the vaccines. These chains of alternating antibodies that can form clots, this theory ONLY uses antibodies and antigens.
Everyone who receives this information and has some influence must do the right thing and immediately call for a HALT to all vaccines using an antigen molecule that is small enough so a single IgG antibody can bind to two antigen molecules, one arm of the IgG antibody to one antigen molecule and the second arm to another antigen molecule. When an antigen molecule is not larger than this described size, it can act as glue between alternating antibodies and form chains of antibodies that can drastically increase the chances of clot formation. For this letter, I will refer to this as a “glue antigen.”
There isn’t a parent on earth who would let their child receive a vaccine booster if they knew this was not just a very rare possibility, but the likely main effect of every booster vaccine with an antigen that is sufficiently small (half the vaccines on earth). If in 200 years of vaccine science, vaccinologists haven’t considered this simple mechanism for clots, then there are a lot of questions that must be asked and answered before vaccines using “glue antigens” are permitted.
Please do the right thing. If you have questions or concerns, please email me back or call me at 213 327 8869.
Thank you,
Regards
/joseph lee/
Electronic signature
Joseph Lee
And my Tweets to him on October 6, 2023.
Dr. Oltz, I emailed you and your colleagues. I will also send by certified mail. I have a critical update for you. I show how strands of alternating antibodies to the spike antigen cause clots. The spike antigen acts as glue to the different antibodies.
I am reaching out to you because this is the exact mechanism causing clots after the booster COVID mRNA vaccine. This is the exact mechanism that caused clots with the J&J vaccine. It is a matter of critical importance and I think this info should be published in your journal
This “String Theory” only uses guaranteed facts. 1. The spike antigen has multiple antigenic sites. 2. Multiple antibodies will form to the spike antigen. 3. Chains of alternating antibodies forming with the spike antigen acting as glue is a guaranteed result.
As a physician, you understand that if a mother understands the ramifications of this discovery, even without more clinical data, no mother on earth would vaccinate their child with the COVID mRNA vaccine. It is not possible for a physician to provide proper informed consent–
if a physician does not have this diagram and explanation. But, this goes beyond the COVID mRNA vaccine. Every childhood vaccine that uses an antigen small enough so that two two separate antigen molecules can bind to one IgG antibody, has this risk.
If I have a theory that if I throw a banana off my roof, that it will fall splat on the ground, the theory uses scientific laws so certain, that I can be certain the banana WILL fall, even if I have NEVER done a single experiment to test this theory.
And the problem is, your Journal should take the ethical, morally responsible action, which is to call for an immediate world-wide halt to all vaccines with antigens that fall under this size criteria. EVEN if this is ONLY a theory so far. The mechanism is TIGHT.
There is PLENTY of data to show that clots result from the vaccine. The anti vaxxers call this the “clot shot.” It is NEVER a good idea NOT to listen to patients when a procedure is done. Half the US calls this the “clot shot” and I found the mechanism —
connecting YOUR vaccine to clots. Meshwork of alternating antibodies glued by your spike antigen. Platelets trapped in the meshwork. FC regions of the antibodies activating FC receptors on platelets. This is all YOUR SCIENCE and YOUR LANGUAGE and YOUR LOGIC.
But, if NO ONE on the pro vaccine side ever does the right thing, do you think the general public will EVER believe what scientists say?? If I am rude, I AM in a hurry because children WILL be getting this clot shot, correct? And please don’t use my rudeness as an excuse.
This ONE DIAGRAM should HALT half the booster vaccines on earth the MOMENT your journal includes my Diagram in a tweet to the Chief Editor, should it not? Until the data on my hypothesis comes out and until their is a reasonable scientific rebuttal, correct?
Being in a rush can always look like rudeness. But, flip and consider how YOU would feel if YOU were ME and discovered this. You would be on FIRE maybe MORE than me, because you KNOW the significance of discovering this mechanism of strands of alternating antibodies.
ah, you know I don’t like to bring up the legal ramifications of this, but you DO realize the Journal of Immunology will face potential lawsuits for BURYING a story this big and so you should act in patients best interests but ALSO in your Journal’s best interests.
and maybe, just maybe, if you don’t do the right thing, the owner of your journal may later sue YOU. Yeah, it gets bizarre. but guess what? When you MANDATE something you know THIS LITTLE about, why wouldn’t you expect lawsuits and a bizarro world?
Elon Musk on Twitter, April 7, 2021. “To be clear, I do support vaccines in general & covid vaccines specifically. The science is unequivocal. In very rare cases, there is an allergic reaction, but this is easily addressed with an EpiPen.”
Aw Elon. you don’t understand medical science. how can you say that the science is unequivocal? the covid vaccine is the biggest mistake in the history of medicine. it supposedly works via a neutralizing antibody in the lung. but the antibody is 8000 times heavier than a water molecule.
and to get into the lung to do it’s neutralizing work, the antibody MUST pass through the lung barrier which can stop water molecules (18 daltons). the covid antibody is a gargantuan 145,000 daltons. NO PATH for the COVID antibody to enter the alveolus.
This IS the current hypothesis under which the COVID vaccine got its EUA from the FDA, via a neutralizing antibody IN THE LUNG that neutralizes the virus before the virus can infect a lung alveolar epithelial cell, the main type of lung cell infected by the virus. unequivocal? far cry.
what IS unequivocal elon is this. it’s utterly stupid to make unequivocal comments in an area that isn’t yours unless you’re willing to OWN your “unequivocal statements”.
I OWN my statements and I AM UNEQUIVOCALLY stating that the COVID vaccine hypothesis is the single biggest mistake in the history of MEDICINE. if you’re not willing to OWN your statements in areas OUTSIDE your area of expertise, don’t make such UNEQUIVOCAL statements. —
yes, free speech is important. and YES you should be RESPONSIBLE (and own) your words that you so freely utter. And the more important the area that you speak those words? the heavier the responsibility for your freely uttered words. make sense Elon? you think you know science?
you’re probably in the top 1 percentile in understanding science. you get that’s a far cry from being able to “own your words” in a field that’s not yours? that that top 1 percentile means that in a group of a million people, 10,000 people know science BETTER than you?
so, if you’re willing to OWN your words that you so freely utter, you’re willing to acknowledge that if you’re wrong about the words you utter, you’re not even in the top 1 percentile (in other words, not smart in science).
if you’re NOT willing to own your words, state clearly that’s the case. don’t back out later and say you didn’t know. which you clearly do not. make sense??? not too complicated? yes, free speech is important. but you become part of the problem when you utter untruths,
The cure for COVID is amazingly simple. In layman’s terms, every fifth grader knows that viruses do NOT grow on their own. They grow within OUR cells. If OUR cells are growing slower during FASTING then our cells grow the virus LESS fast. Then, less of OUR cells are infected with the virus, we are less sick, we cough out less virus particles, our loved ones (those around us) are less sick, and yes, you guessed it. The pandemic is OVER.
For some bizarre reason, the world’s scientists believe that the COVID antibody is somehow extremely important in how our bodies dealt with the COVID virus. Although, everyone who was awake during this Pandemic KNOWS that in the year 2020, NO ONE had a COVID antibody to speak of, when they were infected with COVID for the first time if they weren’t vaccinated (no one in the year 2020 was). Now, over 95% of the U.S. population recovered from COVID in the year 2020 within 10 days (at DAY 10, the COVID antibody was barely showing up). So, this COVID antibody molecule, which was LATE TO THE PARTY somehow got all the credit for saving humanity in 2020? Isn’t this JUST like humans? One person does ALL the work, someone ELSE wants to take ALL the credit? Yeah, apparently molecules play the same game.
In scientific terms, when one is fasting, reactive oxygen species within a cell increase. That results in oxidation of six sulfhydryl groups on the Ribonuclease enzyme Inhibitor. Oxidation of this Inhibitor causes it to RELEASE this PIT BULL, the Ribonuclease enzyme (RNase) and then this GOD given RNase enzyme proceeds to DESTROY ALL mRNA it can find, INCLUDING COVID viral RNA (nice?), INCLUDING OUR mRNA (but we have DNA and can make more RNA?), INCLUDING (and this is the ironic part) COVID Vaccine mRNA within vaccine vials, which is probably why they had to be in a DEEP FREEZE during transport.
Yes, when you are infected with COVID, the next two days, FOOD CAN KILL YOU. Of course, if you’re diabetic, fast under doctor’s orders (the doctor who knows NOTHING about this). And please drink water as necessary. AND, if you LOVE your elderly relatives, make SURE they know this. WHO would eat a hamburger, if they knew that eating it might mean you’re dead in a couple of weeks? Is it a perfect cure? Of course it isn’t. But is anything? And don’t sue me for trying to help (read my disclaimer on lungvirus.com).
What is my proof? 7 billion of us, when we were toddlers and we got sick, 99.99% of us got fussy… AND DID NOT EAT.
ah, great question. 1. convalescent serum first. my mentor from hopkins asked me this and I had a theory of the red blood cell being the ultimate virus trap and defense. so, fragments of other people’s rbc’s would have different antigens and different ability to trap virus
he asked me about a year into the pandemic and was shocked. said it made more sense than what the other directors of medicine were saying.
2. monoclonal antibodies. well, most of them aren’t on the market and they were mostly for mild cases. if a case is mild on day 4, –
it’s not likely to become severe. just the nature of the rate of replication of the virus and how the body is handling it. so, you take a 1000 patients and treat them with ANYTHING on DAY 4 of COVID, but make sure the COVID is MILD, well, you’ve —
drastically reduced the probability of the patient ending up with SEVERE COVID. almost all patients with SEVERE COVID gradually PROGRESSED from DAY ONE. they were NOT mild cases on day four, for the most part. —
now, do I have a PERFECT explanation of how the MONOCLONAL antibody helped? NO. but I can tell you that it DID NOT CROSS the intact blood lung barrier. so, JUST because something seems to WORK, you STILL must provide a hypothesis for HOW you think it worked –
and this monoclonal antibody, isn’t its hypothesis of a NEUTRALIZING ANTIBODY that binds the virus before the virus can infect a lung cell? this is actually quite interesting for me. they can’t really claim there was ANY other type of training, like with the VACCINE. —
It is ACTUALLY an argument for why I AM CORRECT. lol. weird isn’t it? because they can’t claim ANY other TRAINING with the Monoclonal antibody. and they can’t JUST say it TELEPORTS across the lung barrier. so, here’s MY hypothesis for why it SEEMS to work.-
as I previously stated, they cherry picked patients at day four who weren’t going to progress to severe COVID. that’s ONE argument. another one.
Antibodies all increase the risk of complement cascade activation. complement activation results in MANY factors produced —
some of these complement cascade factors include factors that can activate toll receptors, including TLR-4. activation of TLR4 results in production of …. yep. INTERFERON.
See? how in SCIENCE, if you REFUSE to keep an open mind, you WILL go down RABBIT holes and —
end up looking STUPID. I love this Monoclonal antibody issue. can NOT invoke complex training. they always want to invoke COMPLEX training with the vaccine, that they will NEVER put down in writing. but with the Monoclonal? that isn’t an OPTION for the jabbers.
am I saying I’m perfectly correct? no. but I came up with hypothesis that can’t be destroyed simply by thought experiments. THEIR hypothesis of a NEUTRALIZING monoclonal antibody in the lung air space CAN be destroyed by a simple thought experiment since there IS NO PATH–
Mac, GREAT QUESTION. and what a GREAT ASSIST cuz I think I nailed that question. and it is now one of MY weapons in debates against THEM. I LOVE IT.
@AAPNews @AmerAcadPeds @AAPexperience To every Pediatrician in the US. Your leaders are failing you. I presented the SINGLE biggest THREAT to the health of CHILDREN when I discovered the STRING MECHANISM that shows EXACTLY how booster vaccines are causing CLOTS.
@AAPNews @AmerAcadPeds @AAPexperience I’ve already put over 200 posts on the AAPediatrics X account and they have not removed any of them or BLOCKED me because I DO bring LIFE-SAVING INFORMATION FOR CHILDREN.
Do you think a SINGLE parent who sees my video clip will ever want their children vaccinated?
@AAPNews @AmerAcadPeds @AAPexperience The AAPediatrics have had legal opinions and I explained VERY carefully that removing my posts may be interpreted as helping COVER UP the most massive oversight in the history of MEDICINE. That would be “willful misconduct” which invalidates any “legal immunity” via the PREP ACT
@AAPNews @AmerAcadPeds @AAPexperience Your leaders are facing the BIGGEST nightmare for your specialty. How they react and respond to this STRING MECHANISM (that PERFECTLY shows how your booster vaccines are causing clots) will affect your profession FOREVER. I even laid out the ONLY options available to them.
@AAPNews @AmerAcadPeds @AAPexperience Again, to be EXTREMELY CLEAR about this NIGHTMARE STRING MECHANISM that shows that HALF your vaccines are causing clots as their MAIN EFFECT. Parents are observing and keeping screen shots. YOU DO state that your TOP concern is the safety and well-being of children. SHOW IT
@AAPNews @AmerAcadPeds @AAPexperience Because, in a year, every parent on EARTH will know of this ANTIBODY STRING MECHANISM and how the AAPediatrics and AAPNews handles this HUGE NIGHTMARE for CHILDREN, will affect YOUR specialty FOREVER.
@AAPNews @AmerAcadPeds @AAPexperience Here are the ONLY next steps for your specialty.
Immediately call for a HALT to ALL vaccines using an antigen that meets the criteria in the STRING MECHANISM (almost every vaccine that does not use an attenuated virus as the antigen).
@AAPNews @AmerAcadPeds @AAPexperience Inform EVERY one of your 67,000 pediatricians in the US of this NIGHTMARE issue for your specialty, that the most massive oversight in the history of medicine is in your VACCINES. The ANTIBODY STRING MECHANISM explains incredibly simply that oversight.
@AAPNews @AmerAcadPeds @AAPexperience It is IMPOSSIBLE for ANY pediatrician to give adequate INFORMED CONSENT to parents if they fail to mention THIS NEW DISCOVERY, the ANTIBODY STRING MECHANISM and if they fail to show the video clip that shows EXACTLY how CLOTS form after a booster vaccine.
@AAPNews @AmerAcadPeds @AAPexperience With INFORMATION THIS GRAVE and affecting every child in the US who receives a booster vaccine with an antigen fitting the criteria (of the Antibody String Mechanism), is your organization FROZEN BY FEAR? But isn’t the HEALTH of CHILDREN TOP PRIORITY??
@AAPNews @AmerAcadPeds @AAPexperience Today is DAY 10 from when I explained this ANTIBODY STRING MECHANISM to the AAPediatrics. Every day, there is a child who is being vaccinate by a booster (antigen fitting criteria) who is developing a CLOT in a part of their brain (amygdala) and is having a personality change.
@AAPNews @AmerAcadPeds @AAPexperience The Chief Editor, Journal of Immunology was given a 156 pg letter detailing every aspect of this and he has had it for over 10 days. He was unable to provide a scientific rebuttal. It is EXTREMELY unlikely that a single pediatrician among your 67,000 strong will be able to
@AAPNews @AmerAcadPeds @AAPexperience Dr. Eugene Oltz decided to stick his head in the sand and BLOCK me and DELETE my posts and help COVER UP the most massive OVERSIGHT in the history of medicine. I will recommend the DOJ to file CRIMINAL CHARGES against him.
@AAPNews @AmerAcadPeds @AAPexperience Your organization is doing a bit better in that you realized that BLOCKING ME and Deleting my posts would be activity considered to be a COVER UP of the most massive OVERSIGHT in the history of medicine.
@AAPNews @AmerAcadPeds @AAPexperience And that blocking behavior could ALSO be considered by a future jury as “willful misconduct.” The PREP ACT gives organizations “legal immunity” for vaccine related activities, with a MAJOR EXCEPTION, WILLFUL MISCONDUCT CANCELS the LEGAL IMMUNITY.
@AAPNews @AmerAcadPeds @AAPexperience and MUCH more important will be how PARENTS all over the US and the WORLD perceive your specialty, if information THIS CRITICAL to the health of their children is IGNORED and not FORWARDED to every member, all 67,000 Pediatricians in the US.
I’m sorry vigilant. but if there is NO benefit to the COVID vaccine because the COVID antibody can’t enter the lung air space, and RKjr KNOWS this, but doesn’t tell anyone, i just don’t know. what, he wants to KEEP talking about the SIDE EFFECTS? but if everyone knows. NO BENEFIT. who would take it?
what, I come with TOOO much baggage for RKjr? I dislike MALONE. I’m MAD at McCullough for not telling Senator Johnson to work with me. I’m against almost ALL vaccines. too much baggage? why would RKjr NOT take my info? and put it up there? in his nice posters? he doesn’t seem honest to me.
vigilant? thoughts? or will you also go silent on this issue? at what point is it appropriate to call out the opposition leaders?
i mean. clearly the anti-vaxxers aren’t gonna take the COVID shot. is this the way RKjr wants to PUNISH the pro vaxxers? by NOT telling them? that the COVID vaccine has NO BENEFIT? becuz the antibody can’t cross the lung barrier into the lung air space where infections are occurring?
don’t YOU think that EVERYONE in America should know? not JUST the anti-vaxxers? why would RKjr NOT tell America? don’t ALL Americans, EVEN if they’re PRO vaccine, DESERVE to KNOW? so they CAN make their informed choice??? why do you think RKjr is not telling the American Public?
I am ABSOLUTELY sure that RKjr KNOWS my info. HOW? cuz I contacted his attorney a year ago. and his attorney gave me 5 minutes. and I explained everything FAST. there isn’t THAT much to say. I told him in 2 minutes. “what mother would EVER vaccinate their child? “–
“what mother, pro vaccine OR anti vaccine, would EVER vaccinate their child? if the antibody can’t cross the lung barrier because it is a GARGANTUAN 145,000 daltons? and the lung barrier MUST be crossed for the antibody to do its work? but the lung barrier can stop WATER molecules.. “–
Don’t ALL mothers DESERVE to KNOW this CRITICAL information? not JUST the anti-vaxxers? and when RKjr GOT this info from his attorney, who emailed him THAT day, RKjr FORWARDED that email to his dirty dozen, Nass, Malone, McCullough, Kory…..
and then it was DECIDED? that RKjr would NOT work with me? but RKjr MUST be intelligent enough to know what HUGE INFO this is. because ANY mom, educated or not, pro vaccine or anti vax, dem or republican, STILL loves their CHILDREN and would NOT let their child be vaxxed with that CRITICAL INFO
The moment RKjr sent that email to his dirty dozen and cc’ed me. that was one of the happiest days of my past three years. then when they decided NOT to use my info, that was one of my darkest periods.
yes, I APPLAUD RKjr for ALL his work. but, he keeps focusing on RISK. when there IS NO BENEFIT to the vaccine, NO MOTHER ON EARTH would let her child be vaccinated. Isn’t this CRITICAL INFO? is there ANY logical reason for RKjr NOT to BRING UP this info FIRST AND FOREMOST???
and then. I gather myself. and start working again. and get on linkedin. and get booted for life. depressed again. and then. get on twitter oct 2022. and a few weeks later, in ONE day, get 10,000 followers.
and. then Rkjr’s grandson. a producer for children’s defense. david whiteside? white house?? see’s my info. and reaches out for a podcast with RKjr. of COURSE I want to do it. but the back and forth emails slow down. and then stop completely. hmmmmmmmmmm. he got the memo late?? to NOT WORK with me????
and THEN. I have this problem with persistence. so now, I’m annoyed, irritated, curious. what the HELL is going on? so, being IRRITATED because I was ALREADY rejected by RKjr. why is he TEASING ME with his grandson???
AND THEN. My twitter is SUSPENDED for 6 days. Very interesting. Of course I always keep good documentation. so, I videotaped my monitor when they asked me to delete six tweets supposedly with VIOLENCE. which I never wrote.
1.1 what I discovered today. is a hypothesis for WHY athletes are DYING suddenly.
1.2 during mario’s space. normally i would be on FIRE. but just waited. because I had this idea forming. and I couldn’t express it perfectly. but, it still has to come out.
1.3. the hypothesis behind why athletes are dropping. remember. history repeats itself. in the early nineteenth century the NUMBER 1 reason for death for children UNDER 20 was RHEUMATIC heart disease.
1.4 that was ONE antibody to the STREP bacteria. that was the NUMBER ONE killer for children under 20 in the early nineteenth century. look it up. we are RE LIVING THIS SAME SCENARIO.
1.5 A LOT of antibodies make blood MORE viscous. the cardiovascular system is JUST like a PUMP system. any researcher knows ALBUMIN makes the blood THICKER. it is 50 Kdaltons or so.
1.6 COVID antibodies are 150 KDaltons. they make the blood MUCH thicker. so, the heart has to PUMP harder and the wear and tear? ON THE HEART VALVES.
1.7. Thicker more VISCOUS blood will make the HEART that is the PUMP take the BRUNT of the wear and tear. the endothelial lining on the heart blood vessels will be scratched and there WILL BE INFLAMMATION from the INCREASED viscosity.
see? rheumatic heart disease? where supposedly the STREP antibody cross reacted with the HEART valves? I don’t think that’s what happened. I think the INCREASED viscosity HURT the endothelial lining of the heart. which caused INFLAMMATION.
1.9 whenever blood is THICKER the part of the pump system that has the MOST damage is the PUMP. the LINING of the pump (heart) is the endothelium. when it gets scratched OFF, there is INFLAMMATION.
2.0 Covid antibodies are 145,000 daltons. 3 times BIGGER than albumin which increases blood viscosity. do you know how big IgM antibodies are?? 5 COVID antibody molecules
2.1 Boosters create IgM antibodies FIRST which are HUGE and ADD viscosity and DAMAGE primarily the PUMP (heart). that is the HYPOTHESIS for WHY there are SUDDEN DEATHS. INCREASED VISCOSITY of blood.
2.2 I just realized tonite. the STREP antibody probably did NOT have an amazing affinity for the HEART valves. It was JUST that recurrent STREP throat made the body MAKE more antibodies and THAT increased viscosity from the IgM antibodies is PROBABLY what caused HEART DAMAGE.
2.3 The COVID vaccine is mRNA and MORE resistant to being destroyed. they were SOOO amazed that ANY antibodies were produced, they NEVER checked to see if TOOOOO MANY antibodies were produced. they produced TOOOO MANY.
2.4 all the WEIRD sudden deaths? FROM INCREASED VISCOSITY OF BLOOD that had the MOST damaging effects and wear and tear on the PUMP (heart).
2.5 the myocarditis? that is INFLAMMATION. yeah. if VISCOUS blood is being PUMPED HARD through the heart, then endothelial cells are SHEARED OFF and underlying basement membranes exposed and INFLAMMATION
2.6 When they say history repeats itself???? well. Fauci HELPED us REPEAT THIS history. the STREP antibody killed the MOST children in the early nineteenth century. the COVID vaccine probably killed the MOST in the 21st century. VIA SLUDGE IN THE PUMP SYSTEM.
2.7 Do i KNOW this? no. but guess what? science starts with a HYPOTHESIS. and this is a DAMN GOOD hypothesis. so, let’s STOP THE CLOT SHOT the SHIT SHOT until we figure this SHIT OUT.
2.8 and being ONLY human? i fucking do NOT want to EVER talk to STEVE K or Sayed EVER again in my LIFE.
2.9 More problems. My basic belief is that antibodies against viruses are almost pointless. young children’s hearts, are they being damaged? every time you give them a vaccination? but since the YOUNG heart is SO NEW, you don’t see the damage yet?
3.0 So, NOT JUST the COVID vaccine? but ANY vaccine that causes a spike in IgM antibodies? increases the WEAR and TEAR on your heart? Just NOT as obvious with a YOUNG child’s heart?
3.1 When you run a MARATHON, there is WEAR and TEAR on your KNEES and ligaments/joints. Is there WEAR/TEAR on a child’s heart EVERY time they have a SPIKE in IgM antibodies, no matter WHAT infection or vaccine? Just NOT as obvious because the heart is NEW? but WILL age it?
3.2 and to put an exclamation point on this? Rnase enzyme contamination is inconsistent in the vaccine vials. as is amount of time of thawing. as is HOW MUCH RNase is present. problem with that? RNase retains function often EVEN when autoclaved. So, the variability —
3.3 the variability in ACTUAL dose of mRNA delivered to patient comparing high to low amounts given different vials could rarely be a 1000 fold different. and very often could be 10 fold different. do they KNOW????
3.4. It cannot be more ironic. Big pharma considers RNase enzymes to be quite a bother and a contaminant, since it DESTROYS their mRNA vaccine. Yet this enzyme did infinitely more to save humanity than the COVID antibody ever did.
3.5 And the last thread (for now) to tie up the loose ends. thick blood, shearing damage to the lining of the pump, inflammation/myocarditis causing arrythmias, killing via atrial fibrillation/clots and/or ventricular fibrillation/clots– the SUDDEN DEATH.
If your email is on the cc or bcc list, this email is also directed at you. Most of you received a lot of emails from me early in the pandemic. www.lungvirus.com.
All of you infuriated me because I told you many you, if not one scientist at the FDA can explain how a gargantuan 145,000 Dalton IgG COVID antibody molecule could pass through the lung barrier, which can stop water molecules, then the COVID vaccine hypothesis of a neutralizing antibody in the lung space is BROKEN. But, that’s yesterday’s news. Now, I found something even more serious that affects half the vaccines on earth.
This email discloses a simple mechanism that shows exactly how clots form after a COVID mRNA vaccine booster. This mechanism shows that CLOT formation is almost guaranteed, the only uncertainty is how LARGE the clots will be.
I am fairly certain that if you don’t do the correct thing, by the time the public finds out you were informed, it is unlikely that you will be able to keep your job.
Sorry in advance because none of you did the right thing when I sent you my prior information regarding the blood lung barrier and antibody size. Now? I have no sympathy for you when the public decides that you should no longer be a director at the FDA.
Regards,
Joe Lee
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——- Forwarded Message ——- From: Joe Lee, MD <joeleemd@protonmail.com> Date: On Thursday, October 12th, 2023 at 6:14 PM Subject: Critical Update Mechanism for CLOTS following booster vaccines. To: jbc7@cdc.gov <jbc7@cdc.gov>, yyy8@cdc.gov <yyy8@cdc.gov>, Lawrence.Tabak@nih.hhs.gov <Lawrence.Tabak@nih.hhs.gov>, emily.erbelding@nih.hhs.gov <emily.erbelding@nih.hhs.gov>, tucker.carlson@foxnews.com <tucker.carlson@foxnews.com>
To the CDC Director, Dr. Mandy Cohen,
This is critical information re: a nightmare design flaw with the COVID mRNA vaccine resulting in CLOTS.
This is the preface to the 156 page letter attached here. The most important section is the “Lee String Theory.” This String Theory will end half the vaccines on earth this year. This is a matter of utmost importance for protecting American lives and protecting our children.
It is the simplest theory. When you are infected with a COVID virus, since the Spike antigen is attached to the virus particle, you do not form antibodies against the bottom of the spike antigen, you DO form antibodies to the top of the spike antigen.
In a vaccine setting, you have free spike antigen in the blood and lymph and you form antibodies to the TOP of the spike and ALSO to the BOTTOM of the spike antigen. There is no dispute that there are MULTIPLE antigenic sites on the Spike antigen.
Prior to receiving a booster vaccine, we all agree that, without a doubt, these three components are in the blood.
COVID antibodies to the top of the spike antigen are present.
COVID antibodies to the bottom of the spike antigen are present.
Once, the booster is given, spike antigen is added to the above two antibodies. Following a booster COVID mRNA vaccine given within a few months of the first COVID mRNA vaccine, there will be present in the blood at the same time; COVID antibodies to the top of the spike antigen, COVID antibodies to the bottom of the spike antigen, and spike antigen. No vaccine scientist on earth can dispute these three points.
Referring to FIG. 1, the booster vaccine results in the body producing spike antigen that is now present in the blood/lymph. One arm of an IgG (Top) binds to the top of the spike antigen (1). One arm of an IgG (Bottom) binds to the bottom of the same spike antigen (1). The second arm of an IgG (Bottom) binds to another spike antigen (2). One arm of a second IgG (Top) binds to the same spike antigen (2). The second arm of the second IgG (Top) binds to a third spike antigen (3). And the pattern can continue indefinitely, producing thick strands of antibody/antigen complexes. There can be many separate “strings” of alternating IgG (Top) and IgG (Bottom) antibodies. Can you see how this meshwork of strings is the basis for long gelatinous, clots? The chances of this occurring with a real COVID virus infection is very low because the virus particle is too large to act as “glue” between alternating antibodies.
There can be infinite variations of the resulting meshwork patterns and size that can emerge from strings of antibodies formed from the mix of IgG antibodies and IgM antibodies and the spike antigen that act as glue connecting 1) antibodies both IgG and IgM to the top of the spike antigen and 2) antibodies both IgG and IgM to the bottom/side of the spike antigen. The strands of antibodies can be of variable length and some strands may form into balls not that different from balls of string. It is not inconceivable that some of these “balls” of antibodies grow large enough to block blood vessels, with all the downstream damage from blocked blood flow.
Lattice structures formed from immune complexes (antibodies binding to their respective antigen) are a well-known phenomenon and have been extensively studied. Lattice structure formation is affected by many factors. With the COVID spike antigen, we have an extremely unusual situation that dramatically increases the size and length of these structures. With a natural COVID viral infection, antibodies are only formed to the top of the spike antigen. However, free spike antigen generated following the COVID mRNA vaccine results in the production of at least two distinct antibodies, to the top and bottom of the spike antigen. This creates a bizarre situation following administration of the booster COVID mRNA vaccine. There are antibodies now present to the top of the spike antigen and to the bottom (or stalk portion) of the spike antigen.
This opens the possibility for a never-ending weave of lattice structures or strings, until the respective antibodies and spike antigen becomes unavailable due to the formation of extensive lattice structures (and strings of variable length) which create extended clots. The chances of a COVID antibody molecule formed in response to the first COVID vaccine binding a natural COVID virus is at least a million times less than the chances of that same COVID antibody molecule combining with a spike antigen and being found within a meshwork of antibodies. That is why I call this the “Lee string theory that is more fact than theory.” This is why the resulting meshwork of antibodies is the “MAIN EFFECT” of the booster COVID mRNA vaccine. If a side effect of the COVID mRNA vaccine occurred as infrequently as the chance of their COVID antibody binding a COVID virus in the lung, the vaccine scientists would not even list it as a “side effect.” Again, this is exactly why I state that this string formation of antibodies IS THE MAIN EFFECT of the COVID mRNA vaccine.
It is well known that immune complex clearance is affected by the size of the lattice structure. Because of the unusual situation with the free spike antigen resulting in production of at least two different antibodies, immune complexes can criss-cross and form alternating connections with other immune complexes, in ways that would be extremely unlikely if only antibodies to the top of the spike antigen are present. The larger the meshwork of antibodies with spike antigen as the glue connecting the various antibodies, the more unlikely that the normal clearance mechanism can be effective.
The chances of a “double immune complex” forming is much less because if a TOP antibody has two spike antigens bound, one to each arm, for the BOTTOM antibodies two arms to reach the bottom of each spike antigen, the binding would be limited by the angle that the arm projects out, since the body of the antibody would have to be parallel in at least one view, to the TOP antibody.
Similar to how pine needles and leaves can clog gutters and prevent water flow, strings of antibodies, platelets, white blood cells, red blood cells, and coagulation activation can create blockage of blood vessels all over the body. All you have to do is imagine how your shower drain can be blocked by strands of hair and gunk.
This theory ONLY uses facts that are so widely acknowledged that the theory is more fact than theory. For example, I have a theory that if I throw a banana off the roof of my house, it will fall to the ground. I have NEVER studied this. I have done NO research trials on this theory. Yet, I am certain that the banana will fall. In exactly the same way, the chances of an antibody to the spike from the first vaccine actually binding to a real COVID virus is less than 1 in a 1000, probably less than 1 in a million. But the chances of an antibody from the first vaccine binding to a spike antigen from the second vaccine is almost guaranteed. Strands/chains of alternating antibodies are definitely being formed. How large that meshwork is will vary from patient to patient. At a certain critical threshold of meshwork size, clots will form. Again, the strand formation is NOT a side effect. It is in fact the “MAIN EFFECT” of the vaccine to produce an antibody that WILL bind to the spike antigen from the second vaccine.
Without being informed of this breaking new information, it is not possible for a single physician on earth to provide proper informed consent to a prospective COVID vaccine patient. It is NOT my responsibility to perform the additional research to vet this issue; it is the undisputed obligation of the manufacturers of the vaccine (those who make the profit). They listed “clots” as a “side effect” in their warning labels. If the “side effect” of strand formation occurs much more frequently than the “main effect” of the antibody binding to a COVID virus, shouldn’t they be required to UPDATE their warning labels AND report this breaking information to the FDA?
Children in the US receive up to 20 boosters before the age of 4. Half of these booster use vaccines with antigens that can act as glue. Then, under the age of 4, children are exposed to booster vaccines 10 times that can drastically increase their likelihood of clots. A clot in a capillary in brain tissue can cause a personality change, or autism. The potential risk of autism is not from a strange ingredient in the vaccines. These chains of alternating antibodies that can form clots, this theory ONLY uses antibodies and antigens.
Everyone who receives this information and has some influence must do the right thing and immediately call for a HALT to all vaccines using an antigen molecule that is small enough so a single IgG antibody can bind to two antigen molecules, one arm of the IgG antibody to one antigen molecule and the second arm to another antigen molecule. When an antigen molecule is not larger than this described size, it can act as glue between alternating antibodies and form chains of antibodies that can drastically increase the chances of clot formation. For this letter, I will refer to this as a “glue antigen.”
There isn’t a parent on earth who would let their child receive a vaccine booster if they knew this was not just a very rare possibility, but the likely main effect of every booster vaccine with an antigen that is sufficiently small (half the vaccines on earth). If in 200 years of vaccine science, vaccinologists haven’t considered this simple mechanism for clots, then there are a lot of questions that must be asked and answered before vaccines using “glue antigens” are permitted.
Please do the right thing. If you have questions or concerns, please email me back or call me at 213 327 8869.
so, since this IS a free space for science elon? let me discuss what I think is the future of Neuralink.
I’ll do it with a simple analogy.
the human eye will never be transplanted in a million years. how can I back up a statement like that? follow along.
1.2 the connection between the eye and the brain is the optic nerve that is about a mm in diameter. it holds about 1.2 million nerve fibers. imagine a telephone cable that you cut and then try to reattach. doesn’t every line to a different number have to be re-attached correctly?
1.3 exactly the same with the human eye replacement. the optic nerve MUST be cut. then, the NEW eye with its new optic nerve MUST be re-attached. all 1.2 million fibers. everyone in the correct orientation. but guess what? the aren’t labelled. each nerve fiber looks like the next.
1.4 you would have to connect all 1.2 million nerve fibers from the eye donor to the 1.2 million nerve fibers in the optic nerve on the recipient — in the exact right ORIENTATION. and i would suspect tissues would start dying within an hour, but I’ll generously give you four hours.
1.5 in four hours, you would have to connect, NOT nerves, but NERVE FIBERS that are extremely thin, 1.2 MILLION nerve fibers in a span of 4 hours. in a tiny little space, with at most 3 surgeons surrounding the patient.
1.6 each surgeon would have to re-attach 100,000 nerve fibers per hour for four hours, and IDENTIFY the CORRESPONDING FIBER on EACH END. the surgeon would be lucky to find 2 and connect two properly.
1.7 I’ll be generous and say he can do 60. oh, but we are FAR far from 100,000 aren’t we?
some things can NEVER be done no matter HOW amazing science is. those are what we call theoretical limits. and eye transplantation? will NEVER be done in a million years.
1.8 Neuralink will face similar issues. being an eye surgeon, it’s easier to use an eye analogy. but SAME fundamental problem.
see Elon? gotta THINK about things before TWEETING.
This is the issue with the modern world. toooo much data and no one can cut through the data and find meaningful info.
all the opposition leaders. doing the same thing. not saying it’s not completely useless. Just saying that they ALL are collecting data. cases of death from the vaccine. not saying that’s useless. —
It’s about efficiency. The antibody has no path into the lung. what a HUGE mistake. yes, by all means point out all the RISKS with the vaccine. but, when there isn’t a benefit? the lack of a benefit makes ALL THE RISKS that all the opposition leaders find EVEN MORE STARTLING.
so, you would think that people like STEVE Kirsch would EMBRACE what I found and USE IT to FURTHER their OWN agenda of stopping the vaccine. but they don’t. that’s where the EGO comes in and becomes a problem.
the covid antibody has no path through the lung barrier. fauci was informed in 73 pges feb 2021 with US copyrights. YET, he proceeds. the vaccine is a biological compound. he DID hurt people with it KNOWINGLY. Then he USED it as a biological weapon. that is BLACK AND WHITE.
and the MOST frustrating thing for me? I call out THEIR stupidity in overlooking that the neutralizing antibody has no path into the lung. they have no response. the idiots lower down excuse it by saying, the immune system is more complex than you know. I GET THAT. —
I’m the ones TELLING THEM they have NO IDEA how it works and they just come back with, IT IS COMPLEX. I say, WRITE IT DOWN. EXPLAIN IT. GO REPEAT YOUR FDA EUA PROCESS SINCE YOU GOT YOUR FIRST EUA based on a neutralizing antibody in the LUNG. and they never can explain it.
and the concept of “training” and “memory” is what I use against them. There are well over 300 million lung alveolar epithelial cell. I tell them, where are your trained white blood cells? I’ll ASSUME for YOU that they are TRAINED. then, 300 million lung cells —
300 million lung cells would HAVE to be INTERVIEWED by these “trained” white cells since one viral strand can easily become 50,000 virus particles in ONE infected lung cell. And you have to describe HOW that trained white cell determines WHICH lung cells to kill. —
you are NOT just allowed to say the human organism is TRAINED. you have to DETAIL EXPLAIN IT so it makes LOGICAL SENSE. WHERE IS THE TRAINING? If it’s in white cells, the INTERVIEWING process is IMPOSSIBLE. If the “training” is in a molecule, there is ONLY one molecule–
only ONE molecule type, the antibodies, that have ANY evidence of being “trained” by a past infection and having “memory”. Interferon molecules and chemokines do NOT. so, they have NO clue on how this “training” occurs. they ALWAYS discuss “TRAINING” but can’t even–
they can’t even BEGIN to explain in the most BASIC terms HOW this “training” occurs and can’t explain the MOST basic flow of the strategy implemented by either trained white cells or trained molecules, in a recurrent infection. It is BIZARRE to me —
it is BIZARRE that the ONLY thing the jabbers will say, is that you “learned” from the vaccine. but NO ONE can elucidate HOW this occurs? and when I exposed the stupidity of the “trained molecule” portion of this “training”, the only answer? you don’t know. WHO DOES????
and I do NOT know because I do NOT think it’s possible. I PROPOSE the most BASIC possibilities, that of TRAINED WHite cells that go INTERVIEW and destroy or NOT destroy infected cells, but the logistics of that process demonstrate it is VIRTUALLY IMPOSSIBLE.
So, what is OBVIOUS to me now is this. THEY DO NOT HAVE AN ANSWER. they did NOT even do what I did, create a possible (impossible) hypothesis of HOW this “training” would manifest in a real re-infection. THEY HAVE NO ANSWER, NO HYPOTHESIS, JUST, “it is complex”.
and the most fundamental reason why the “trained” white cell interviewing 300 million lung cells (minimum) and killing off the lung cells that are tooo infected, the reason why this is VIRTUALLY impossible, because it would have to be REPEATED every TWO OR THREE DAYS.
Do you get the irony of what you did? I’ve been locked out for what 10 days? because my account was hacked? and I IMMEDIATELY informed you? and emailed you MANY times for a status update with NO response?
but then, you ACTIVATE my suspended account. at 4:15 am THIS morning, you ACTIVATE my account. with NO correspondence with me and NO attempt to reach me. I find out after 12:00 PM. When I try to sign on, clearly it’s DIFFICULT.
I finally CHANGE the password since I DO have access to my email. the HACKER must have had access to my account with the OLD password that HE created. apparently you gave the HACKER time to change my profile PIC and my profile NAME to something that VIOLATES twitter rules.
Then, when I FINALLY have access to my account after noon today, you will NOT let me change the profile pic that is the twitter logo. and you will NOT let me change back to @leelasik.
sneaky. but, remember. I’m the guy that figured out the FLAW with the COVID vaccine. You don’t think I’m going to figure out your little shenanigans???
LOL.
Twitter censors. you will come out looking EXTREMELY bad when all this is sad and done.
From: Joe Lee, MD <joeleemd@protonmail.com> Date: On Thursday, October 12th, 2023 at 11:34 PM Subject: Fw: Critical Update Mechanism for CLOTS following booster vaccines.
To ALL employees of the FDA (if you have received this email, this letter is directed to you),
There is NO training like on the job training. I present the single biggest flaw in the history of medicine. I show the exact mechanism for the formation of clot after a booster vaccine.
As you can see from the figure, when you are given a COVID mRNA vaccine, the spike antigen is NOT attached to a virus and so antibodies can form to the top and the bottom of the spike antigen.
When the booster COVID mRNA vaccine is given, you have in your blood, antibodies to both the top and the bottom of the spike antigen. Then, you are given the booster vaccine which creates spike antigen in your blood. With those three components, I show the chains of alternating antibodies, glued together by the spike antigen. Yes, the SINGLE BIGGEST mistake in the history of medicine.
Now, every one of you is informed. Your bosses may not want to do the right thing. What do YOU think YOU should do? Because when the public finds out that not ONE person at the FDA wanted to alert the media to this CATASTROPHIC ISSUE, then each one of you who got my email will probably lose your job. Will ONE of you take the ONLY ETHICAL action left? To call for an IMMEDIATE HALT of all vaccine boosters with an antigen molecule small enough that a single antibody molecule can bind two distinct antigen molecules thus enabling the long chains of alternating antibodies? This meshwork will trap platelets. Platelets will be activated by the FC regions of the antibodies. CLOT formation after a booster vaccine is NOT a side effect. IT IS THE MAIN EFFECT as can be so clearly seen in my ONE DIAGRAM that will end HALF THE VACCINES ON EARTH.
DO THE RIGHT THING. The public will make you pay the price for not taking the only ethical action. GOOD LUCK. This is REAL LIFE and you are supposed to PROTECT the American people. And, protecting the public will also mean PROTECTING YOUR JOB. Your next action can be as simple as forwarding to the responsible party and then FOLLOWING UP TO SEE THAT THEIR ACTIONS ARE APPROPRIATE. Because, there is only ONE ETHICAL NEXT STEP, to call for the IMMEDIATE HALT of all vaccines using antigens fitting this criteria (half of all vaccines on earth).
Very disappointed in the NIH, CDC and FDA.
Regards,
/joseph lee/
electronic signature.
Joseph Lee, MD
——- Forwarded Message ——- From: Joe Lee, MD <joeleemd@protonmail.com> Date: On Thursday, October 12th, 2023 at 8:31 PM Subject: Fw: Critical Update Mechanism for CLOTS following booster vaccines. To: Alcock, Patricia L. <Patricia.Alcock@fda.hhs.gov>, Loney.NUNEMAKER@FDA.HHS.Gov <Loney.NUNEMAKER@FDA.HHS.Gov>, Thomas.HUGHES@FDA.HHS.Gov <Thomas.HUGHES@FDA.HHS.Gov>, Erin.FERGUSON@FDA.HHS.Gov <Erin.FERGUSON@FDA.HHS.Gov>, Michelle.Gamble@fda.hhs.gov <Michelle.Gamble@fda.hhs.gov>, Kristin.Hughes@fda.hhs.gov <Kristin.Hughes@fda.hhs.gov>
Dear FDA Directors,
If your email is on the cc or bcc list, this email is also directed at you. Most of you received a lot of emails from me early in the pandemic. www.lungvirus.com
All of you infuriated me because I told you, if not one scientist at the FDA can explain how a gargantuan 145,000 Dalton IgG COVID antibody molecule could pass through the lung barrier, which can stop water molecules, then the COVID vaccine hypothesis of a neutralizing antibody in the lung space is BROKEN. But, that’s yesterday’s news. Now, I found something even more serious that affects half the vaccines on earth.
This email discloses a simple mechanism that shows exactly how clots form after a COVID mRNA vaccine booster. This mechanism shows that CLOT formation is almost guaranteed, the only uncertainty is how LARGE the clots will be.
I am fairly certain that if you don’t do the correct thing, by the time the public finds out you were informed, it is unlikely that you will be able to keep your job.
Sorry in advance because none of you did the right thing when I sent you my prior information regarding the blood lung barrier and antibody size. Now? I have no sympathy for you when the public decides that you should no longer be a director at the FDA.
Regards,
Joe Lee
——- Forwarded Message ——- From: Joe Lee, MD <joeleemd@protonmail.com> Date: On Thursday, October 12th, 2023 at 6:14 PM Subject: Critical Update Mechanism for CLOTS following booster vaccines. To: jbc7@cdc.gov <jbc7@cdc.gov>, yyy8@cdc.gov <yyy8@cdc.gov>, Lawrence.Tabak@nih.hhs.gov <Lawrence.Tabak@nih.hhs.gov>, emily.erbelding@nih.hhs.gov <emily.erbelding@nih.hhs.gov>, tucker.carlson@foxnews.com <tucker.carlson@foxnews.com>
To the CDC Director, Dr. Mandy Cohen,
This is critical information re: a nightmare design flaw with the COVID mRNA vaccine resulting in CLOTS.
This is the preface to the 156 page letter attached here. The most important section is the “Lee String Theory.” This String Theory will end half the vaccines on earth this year. This is a matter of utmost importance for protecting American lives and protecting our children.
It is the simplest theory. When you are infected with a COVID virus, since the Spike antigen is attached to the virus particle, you do not form antibodies against the bottom of the spike antigen, you DO form antibodies to the top of the spike antigen.
In a vaccine setting, you have free spike antigen in the blood and lymph and you form antibodies to the TOP of the spike and ALSO to the BOTTOM of the spike antigen. There is no dispute that there are MULTIPLE antigenic sites on the Spike antigen.
Prior to receiving a booster vaccine, we all agree that, without a doubt, these three components are in the blood.
COVID antibodies to the top of the spike antigen are present.
COVID antibodies to the bottom of the spike antigen are present.
Once, the booster is given, spike antigen is added to the above two antibodies. Following a booster COVID mRNA vaccine given within a few months of the first COVID mRNA vaccine, there will be present in the blood at the same time; COVID antibodies to the top of the spike antigen, COVID antibodies to the bottom of the spike antigen, and spike antigen. No vaccine scientist on earth can dispute these three points.
Referring to FIG. 1, the booster vaccine results in the body producing spike antigen that is now present in the blood/lymph. One arm of an IgG (Top) binds to the top of the spike antigen (1). One arm of an IgG (Bottom) binds to the bottom of the same spike antigen (1). The second arm of an IgG (Bottom) binds to another spike antigen (2). One arm of a second IgG (Top) binds to the same spike antigen (2). The second arm of the second IgG (Top) binds to a third spike antigen (3). And the pattern can continue indefinitely, producing thick strands of antibody/antigen complexes. There can be many separate “strings” of alternating IgG (Top) and IgG (Bottom) antibodies. Can you see how this meshwork of strings is the basis for long gelatinous, clots? The chances of this occurring with a real COVID virus infection is very low because the virus particle is too large to act as “glue” between alternating antibodies.
There can be infinite variations of the resulting meshwork patterns and size that can emerge from strings of antibodies formed from the mix of IgG antibodies and IgM antibodies and the spike antigen that act as glue connecting 1) antibodies both IgG and IgM to the top of the spike antigen and 2) antibodies both IgG and IgM to the bottom/side of the spike antigen. The strands of antibodies can be of variable length and some strands may form into balls not that different from balls of string. It is not inconceivable that some of these “balls” of antibodies grow large enough to block blood vessels, with all the downstream damage from blocked blood flow.
Lattice structures formed from immune complexes (antibodies binding to their respective antigen) are a well-known phenomenon and have been extensively studied. Lattice structure formation is affected by many factors. With the COVID spike antigen, we have an extremely unusual situation that dramatically increases the size and length of these structures. With a natural COVID viral infection, antibodies are only formed to the top of the spike antigen. However, free spike antigen generated following the COVID mRNA vaccine results in the production of at least two distinct antibodies, to the top and bottom of the spike antigen. This creates a bizarre situation following administration of the booster COVID mRNA vaccine. There are antibodies now present to the top of the spike antigen and to the bottom (or stalk portion) of the spike antigen.
This opens the possibility for a never-ending weave of lattice structures or strings, until the respective antibodies and spike antigen becomes unavailable due to the formation of extensive lattice structures (and strings of variable length) which create extended clots. The chances of a COVID antibody molecule formed in response to the first COVID vaccine binding a natural COVID virus is at least a million times less than the chances of that same COVID antibody molecule combining with a spike antigen and being found within a meshwork of antibodies. That is why I call this the “Lee string theory that is more fact than theory.” This is why the resulting meshwork of antibodies is the “MAIN EFFECT” of the booster COVID mRNA vaccine. If a side effect of the COVID mRNA vaccine occurred as infrequently as the chance of their COVID antibody binding a COVID virus in the lung, the vaccine scientists would not even list it as a “side effect.” Again, this is exactly why I state that this string formation of antibodies IS THE MAIN EFFECT of the COVID mRNA vaccine.
It is well known that immune complex clearance is affected by the size of the lattice structure. Because of the unusual situation with the free spike antigen resulting in production of at least two different antibodies, immune complexes can criss-cross and form alternating connections with other immune complexes, in ways that would be extremely unlikely if only antibodies to the top of the spike antigen are present. The larger the meshwork of antibodies with spike antigen as the glue connecting the various antibodies, the more unlikely that the normal clearance mechanism can be effective.
The chances of a “double immune complex” forming is much less because if a TOP antibody has two spike antigens bound, one to each arm, for the BOTTOM antibodies two arms to reach the bottom of each spike antigen, the binding would be limited by the angle that the arm projects out, since the body of the antibody would have to be parallel in at least one view, to the TOP antibody.
Similar to how pine needles and leaves can clog gutters and prevent water flow, strings of antibodies, platelets, white blood cells, red blood cells, and coagulation activation can create blockage of blood vessels all over the body. All you have to do is imagine how your shower drain can be blocked by strands of hair and gunk.
This theory ONLY uses facts that are so widely acknowledged that the theory is more fact than theory. For example, I have a theory that if I throw a banana off the roof of my house, it will fall to the ground. I have NEVER studied this. I have done NO research trials on this theory. Yet, I am certain that the banana will fall. In exactly the same way, the chances of an antibody to the spike from the first vaccine actually binding to a real COVID virus is less than 1 in a 1000, probably less than 1 in a million. But the chances of an antibody from the first vaccine binding to a spike antigen from the second vaccine is almost guaranteed. Strands/chains of alternating antibodies are definitely being formed. How large that meshwork is will vary from patient to patient. At a certain critical threshold of meshwork size, clots will form. Again, the strand formation is NOT a side effect. It is in fact the “MAIN EFFECT” of the vaccine to produce an antibody that WILL bind to the spike antigen from the second vaccine.
Without being informed of this breaking new information, it is not possible for a single physician on earth to provide proper informed consent to a prospective COVID vaccine patient. It is NOT my responsibility to perform the additional research to vet this issue; it is the undisputed obligation of the manufacturers of the vaccine (those who make the profit). They listed “clots” as a “side effect” in their warning labels. If the “side effect” of strand formation occurs much more frequently than the “main effect” of the antibody binding to a COVID virus, shouldn’t they be required to UPDATE their warning labels AND report this breaking information to the FDA?
Children in the US receive up to 20 boosters before the age of 4. Half of these booster use vaccines with antigens that can act as glue. Then, under the age of 4, children are exposed to booster vaccines 10 times that can drastically increase their likelihood of clots. A clot in a capillary in brain tissue can cause a personality change, or autism. The potential risk of autism is not from a strange ingredient in the vaccines. These chains of alternating antibodies that can form clots, this theory ONLY uses antibodies and antigens.
Everyone who receives this information and has some influence must do the right thing and immediately call for a HALT to all vaccines using an antigen molecule that is small enough so a single IgG antibody can bind to two antigen molecules, one arm of the IgG antibody to one antigen molecule and the second arm to another antigen molecule. When an antigen molecule is not larger than this described size, it can act as glue between alternating antibodies and form chains of antibodies that can drastically increase the chances of clot formation. For this letter, I will refer to this as a “glue antigen.”
There isn’t a parent on earth who would let their child receive a vaccine booster if they knew this was not just a very rare possibility, but the likely main effect of every booster vaccine with an antigen that is sufficiently small (half the vaccines on earth). If in 200 years of vaccine science, vaccinologists haven’t considered this simple mechanism for clots, then there are a lot of questions that must be asked and answered before vaccines using “glue antigens” are permitted.
Please do the right thing. If you have questions or concerns, please email me back or call me at 213 327 8869.
There is a reason why I make so many political comments. the frame of mind that allows this (the DEMS) IS A PROBLEM and LEADS TO EVIL and ULTIMATELY leads to MODERN HUMAN CHILD SACRIFICE.
If anyone thinks that I stated something over the top, that I need to be censored by twitter for that comment about human child sacrifice, do you believe that the infants who suffer severe side effects from the HEP B vaccine (when the MOM did NOT have HEP B) and the infants who happen to die–
do you think those infant deaths are justified by benefit (from the HEP B vax) to the infant or benefit to those surrounding the infant? then, state what the benefit is. ah. you can’t. Becuz there is none. then. how is that different from ancient rites of child sacrifice?
then, isn’t the use of HEP B vaccines in infants (with a mother that is HEP B free), isn’t that medical practice identical to that ancient practice of human child sacrifice?
at least for the ancients, although there was NOT a clear scientific benefit to murdering a child, there was a vague mystical idea/belief that this murderous act would bring good to the group.
in the HEP B vaccine infant murders, there is NOT a clear scientific benefit to murdering the infant. there isn’t even a vague mystical idea/belief that this murderous act would bring good to the group. isn’t this CURRENT situation even MORE EVIL? than the ancient rite of human child sacrifice?
The first vaccine slayer is the “Lee String Theory” that is more fact than theory.
This twin is almost as powerful as the first twin (the Lee String Theory can single-handedly take down half the vaccines on earth). But no Super Hero likes to fight alone. Luckily, the Lee String Theory has an equally potent twin and the two twins cover each other’s weaknesses perfectly.
There isn’t a vaccine scientist on earth that can withstand these superhero Vaccine Slayer Twins. This one is called the Middle-Man Theory. He covers everything that the Twin Theory doesn’t cover. And I mean EVERYTHING. Not like the String Theory meshwork isn’t powerful, it is.
But, between these two twins, they are like the tag-team duo to beat all tag team vaccines. and the incredible part is that this duo? doesn’t use ANY magic. No weird additive, NOTHING unscientific. This duo just uses EXACTLY what the vaccine scientists use and REVERSES IT on THEM.
Of course, justice can’t be done trying to describe this fantastic duo in a couple of pages, but don’t you worry. There is a lot more detail spelled out in my gargantuan 150+ page letter to all major retail pharmacies. It is sufficiently detailed to allow the possibility of criminal prosecution against —
—all organizations and persons receiving this letter. So, help me get the word out. Get copies of this 150+ page letter and send to your least favorite immunologist, pediatrician, and nerd who are strong proponents of this Bioweapon, the COVID VACCINE.
This duo is SO powerful, all vaccines on earth will shudder in fear at the mere mention of this duo. The ramifications of understanding what this duo is capable of doing will send shivers down the spine of every pediatrician and vaccinologist alive.
There isn’t a mother on earth who can read that will read about these two, who will STILL want to have their children vaccinated for ANYTHING, until the vaccine industry comes out with a white paper trying to REBUT this. An impossible task, though.
It can be described in two tweets. The Middle-Man Theory is an incredible alter-ego to his Twin, The String Theory. Some people counter the String Theory by saying that when the vaccine mRNA inside a cell produces spike antigen, that spike antigen STAYS on the cell surface.
Didn’t the FIRST vaccine produce antibodies to the top of the spike antigen? Then, when you receive the SECOND mRNA vaccine, will not MORE cells produce spike antigen on their surface that stays attached? Such a simple theory. You DO have antibodies to the spike before the 2nd vaccine?
Then, after the SECOND mRNA vaccine, now you create MORE human cells that have spike antigen attached to the cell, NOT FREE. Fine. Then antibodies made from the FIRST vaccine WILL attach to the attached spike antigen on the cell, yes?
And that is the MIDDLE-MAN THEORY. Because once you have a COVID antibody attached to the spike antigen on a human cell, you have JUST called in the ARMY, the NAVY and the MARINES. You have JUST tricked your body into believing that this poor cell needs to be KILLED.
Every antibody Fc-mediated function is now activated. Here’s an example. Antibody dependent cellular cytotoxicity (ADCC). Antibody Fc-dependent activation of effector cells. Antibody mediated Natural Killer Cell activation. This is too easy, isn’t it?
EVERY cell in the human that has Fc-receptors (and can move) can come and kill these cells that are producing spike antigen and when the cell attaches these spike antigens to its cell membrane, these immune cells come and kill the poor human cell that is expressing this spike antigen.
Wow. The TRAINING uses REAL BULLETS. and REAL HUMAN CELLS have to DIE during the “training” exercise. It gets CRAZIER. This MIDDLE-MAN is NO JOKE. Now, imagine a free spike antigen which DEFINITELY OCCURS. Does it NOT bind the ACE2 Receptor?
Can’t OTHER antigenic sites on this spike produce OTHER antibodies, not JUST to the top? Then, this free SPIKE antigen, it WILL bind to ACE2 receptors on cells all OVER the body? LUNGS, kidneys, testes, liver, heart.
Then when this SPIKE antigen binds to those ACE2 receptors and antibodies to OTHER parts of the spike antigen are present, OTHER than the ACE2 binding site, won’t all the white blood cells start DESTROYING these tissues via ADCC?
This is the MIDDLE MAN THEORY, shows that the TRAINING they think is going on is literally a REAL BATTLE with REAL DAMAGE to REAL TISSUES because blanks are NOT BEING USED. Vaccines are NOT TRAINING OUR CELLS. Vaccines are DESTROYING OUR CELLS.
This is also my hypothesis for many of the varied symptoms from various viral infections, like HEP B where the HEP B surface antigen (HBsAg) will DEFINITELY bind to liver cells and once bound, there WILL BE antibodies that form to the visible part of the HBsAg on the liver cell.
Again, in the interests of humanity, I am QUICKLY releasing this information. It will turn out to be the mechanism of damage for MANY OTHER DISEASES.
The LEE String Theory that is more Fact than Theory, Again CLOTS
What was the point of the booster COVID mRNA vaccine given within two months of the first vaccine? Wasn’t the goal to increase the amount of COVID neutralizing antibodies? It’s hard to imagine another goal than that, but please correct me if I am mistaken. Let’s assume that was their goal in administering a second COVID mRNA vaccine with a few months of the first vaccine, the “booster” vaccine. Let me explain how the “booster” vaccine given within a few months of the first vaccine actually drastically decreased the amount of COVID antibody in the blood for at least a few weeks and simultaneously dramatically increased the risk of CLOTS and tissue damage downstream from the CLOTS.
Here is the bizarre twist. As I described in the previous section, having free spike antigen (as opposed to the antigen being attached to a virus particle) allows formation of antibodies to both the top of the spike antigen and the bottom of the spike antigen, at the absolute minimum. When a COVID virus presents the spike antigen to B-lymphocytes, only the TOP of the spike antigen is presented for later antibody production. But, for a free spike antigen not attached to a virus particle, all sides of the spike antigen molecule can produce corresponding antibodies. It is impossible for a vaccine scientist to argue this point and say otherwise.
Following the first COVID mRNA vaccination, a patient formed COVID antibodies to both the TOP and the BOTTOM of the COVID free spike antigen. Many more distinct antibodies may have formed, but we only need these two and the spike antigen to produce strings.
Following the second COVID mRNA vaccine, we are absolutely certain of three facts.
1) COVID antibodies to the top of the spike antigen are present.
2) COVID antibodies to the bottom of the spike antigen are present.
3) Free spike antigen is present. What a tangled web (of antibodies) we weave once we begin to deceive (the liar that pretended he was a good scientist for 38 years, fauci).
It cannot be refuted. Following a booster COVID mRNA vaccine given within a few months of the first COVID mRNA vaccine, there will be present in the blood at the same time COVID antibodies to the top of the spike antigen, COVID antibodies to the bottom of the spike antigen, and spike antigen. No vaccine scientist on earth can dispute these three points.
Referring to FIG. 1, the booster vaccine results in the body producing spike antigen that is now present in the blood/lymph. One arm of an IgG (Top) binds to the top of the spike antigen (1). One arm of an IgG (Bottom) binds to the bottom of the same spike antigen (1). The second arm of an IgG (Bottom) binds to another spike antigen (2). One arm of a second IgG (Top) binds to the same spike antigen (2). The second arm of the second IgG (Top) binds to a third spike antigen (3). And the pattern can continue indefinitely, producing thick strands of antibody/antigen complexes. There can be many separate “strings” of alternating IgG (Top) and IgG (Bottom) antibodies. Can you see how this meshwork of strings is the basis for long gelatinous, clots?
There can be infinite variations of the resulting meshwork patterns and size that can emerge from strings of antibodies formed from the mix of IgG antibodies and IgM antibodies and the spike antigen that act as glue connecting 1) antibodies both IgG and IgM to the top of the spike antigen and 2) antibodies both IgG and IgM to the bottom/side of the spike antigen. The strands of antibodies can be of variable length and some strands may form into balls not that different from balls of string. It is not inconceivable that some of these “balls” of antibodies grow large enough to block blood vessels, with all the downstream damage from blocked blood flow.
Lattice structures formed from immune complexes (antibodies binding to their respective antigen) are a well-known phenomenon and have been extensively studied. Lattice structure formation is affected by many factors. With the COVID spike antigen, we have an extremely unusual situation that dramatically increases the size and length of these structures. With a natural COVID viral infection, antibodies are only formed to the top of the spike antigen. However, free spike antigen generated following the COVID mRNA vaccine results in the production of at least two distinct antibodies, to the top and bottom of the spike antigen. This creates a bizarre situation following administration of the booster COVID mRNA vaccine. There are antibodies now present to the top of the spike antigen and to the bottom (or stalk portion) of the spike antigen.
This opens the possibility for a never-ending weave of lattice structures or strings, until the respective antibodies and spike antigen becomes unavailable due to the formation of extensive lattice structures (and strings of variable length) which create extended clots. The chances of a COVID antibody molecule formed in response to the first COVID vaccine binding a natural COVID virus is at least a million times less than the chances of that same COVID antibody molecule combining with a spike antigen and being found within a meshwork of antibodies. That is why I call this the “Lee string theory that is more fact than theory.” This is why the resulting meshwork of antibodies is the “MAIN EFFECT” of the booster COVID mRNA vaccine. If a side effect of the COVID mRNA vaccine occurred as infrequently as the chance of their COVID antibody binding a COVID virus in the lung, the vaccine scientists would not even list it as a “side effect.” Again, this is exactly why I state that this string formation of antibodies IS THE MAIN EFFECT of the COVID mRNA vaccine.
It is well known that immune complex clearance is affected by the size of the lattice structure. Because of the unusual situation with the free spike antigen resulting in production of at least two different antibodies, immune complexes can criss-cross and form alternating connections with other immune complexes, in ways that would be extremely unlikely if only antibodies to the top of the spike antigen are present. The larger the meshwork of antibodies with spike antigen as the glue connecting the various antibodies, the more unlikely that the normal clearance mechanism can be effective.
Suppose a patient is deficient in certain complement factors. In that case, the normal process of removing “immune complexes” from the blood is markedly diminished, and the build-up of pathologic immune complexes will lead to glomerulonephritis and vasculitis throughout the body. Since the booster COVID mRNA vaccine produces “immune complexes,” giving the booster without knowing whether a patient has adequate complement factors will put the patient at a significantly higher risk for tissue damage, especially given the extended meshwork of antibodies that will inevitably form. Giving the COVID booster mRNA vaccine to a patient with deficient complement factors can result in a build-up of pathologic immune complexes, which can further cause glomerulonephritis (including the risk of kidney failure) and vasculitis. The presence of vasculitis in the coronary vessels can lead to heart attacks.
Similar to how pine needles and leaves can clog gutters and prevent water flow, strings of antibodies, platelets, white blood cells, red blood cells, and coagulation activation can create blockage of blood vessels all over the body. All you have to do is imagine how your shower drain can be blocked by strands of hair and gunk.
Every vaccine that provides an antigen with more than one antigenic site (almost every vaccine) creates this identical situation when a booster is given within a few months of the first vaccine (if the antigen is small enough so that each arm of the antibody can bind to separate antigen molecules). All booster vaccines using antigens fitting this size criteria should be immediately stopped worldwide until this is completely vetted.
There will be many more important medical discoveries from this hypothesis but in the interests of quickly preventing more patient suffering/death, I am releasing this information now.
1.1 It is THIS simple. BENEFIT. WHERE IS THE BENEFIT? where is the BENEFIT of the COVID vaccine? No. don’t show me DATA. SHOW ME THE HYPOTHESIS. SHOW ME HOW? SHOW ME THE biochemical PATHWAY.
1.2 You can ask a 100 physicians how penicillin works. THE ACTUAL pathway. They will be EMBARRASSED to say “it just works”. they won’t EVEN think it’s acceptable to say that.
1.3 And because amoxicillin works WELL and at least half the physicians can explain in detail how it works. If they don’t know, ANYONE can GOOGLE the actual MECHANISM for how amoxicillin works. it is THAT STRAIGHTFORWARD. that IS SCIENCE.
1.4 and with amoxicillin, you have mothers BEGGING for the amoxicillin. you do NOT have to mandate that stuff. because there is excellent science behind it. excellent science means there is a MECHANISM.
1.5 Amoxicillin? NEVER A NEED TO MANDATE IT. BECAUSE IT HAS EXCELLENT SCIENCE BEHIND IT. and IT WORKS. and MOTHERS ARE CLAMORING FOR IT.
1.6 The COVID vaccine? try to look up how it works. they will explain that it “trains” you. that is NOT an explanation. HOW DOES IT TRAIN YOU? where is the BENEFIT?
1.7 If the BENEFIT is so straightforward, why do so many people who get vaccinated ALSO then become infected with COVID? and EVERYONE on earth knows this can happen.
1.8 And if the BENEFIT is sooo amazing, WHY IS IT MANDATED?
WHERE is the MECHANISM for the BENEFIT of the COVID VACCINE???
And. the neutralizing antibody in the lung IS the hypothesis under which the COVID vaccine was given the EUA. and THAT hypothesis IS DEAD.
1.9 There has NEVER been a publication showing an active transport system that can FERRY these COVID antibodies across the lung barrier into the LUNG air space. THEIR original hypothesis to show the BENEFIT of the COVID vaccine is DEAD. where is their CURRENT hypothesis?
and I let fauci know of this flaw in OCT of 2020. and AGAIN in FEB 2021. WITH us COPYRIGHT to prove date.
2.0 And I started by saying what? DO NOT SHOW ME DATA. SHOW ME YOUR HYPOTHESIS. Why? It’s like the RAINDANCERS of old. 100% AWESOME DATA. but it was a FALSE POSITIVE. The raindancers had NOTHING to do with the RAIN. and the vaccine does NOT work because of “training”.
2.1 And IF the vaccine worked because of its SIDE EFFECT of the hundreds of potential chemokines the body produced in response to the vaccine, and some of these chemokines were ANTIVIRAL, but NONE of these molecules have MEMORY aside from the ANTIBODY, then –
2.2 then, it did NOT work because of the “training” “memory” portion of the vaccine and there WILL BE NO MEMORY, so it is working as a MEDICINE in which case there is NO POINT in giving it when you don’t have the ILLNESS.
Science means your thoughts reflect reality accurately. If one’s thoughts happen NOT to match reality and someone else EXPOSES you for that, the next action for a scientist is NOT to CENSOR or BAN or SUSPEND the person who corrects your mistake in understanding. That’s what ELON MUSK just did to me because I explained why I thought NEURALINK would NEVER work.
So, since ELON decided to BAN me from TWITTER ILLEGALLY, I will pursue a lawsuit against Twitter. But more than that, let me explain why TESLA is NOT GREEN.
Have you ever purchased a car with the interior a very DARK color? have you noticed how HOT the inside of the car becomes just from being in the sun? compared to a car with a lighter interior? Yes, that is because the SUN’s energy is ABSORBED by the dark interior paint and STAYS in the car.
Solar panels? are they NOT dark? do they NOT absorb the energy from the SUN? and KEEP in on earth? ah. this calculation was NEVER done by a SINGLE EV manufacturer OR by a SINGLE critic of EVs. Yes, EVEN assuming that ALL the electricity that is used in EVs is ALL from solar energy, you MUST consider that this solar energy would have been REFLECTED back into SPACE by the acres of sand that the SOLAR panels are placed on. but, with the DARK solar panels, that otherwise reflected solar energy that would LEAVE earth and NOT increase global warming? guess what??? that ENERGY that would have OTHERWISE LEFT EARTH via reflection is now TRAPPED by the solar panel and that energy is KEPT ON EARTH.
Yes. if you want to PROVE that EVs decrease global warming, you’ve got to do your SCIENCE CORRECTLY. ELON. so, advertising EVs as helping DECREASE GLOBAL WARMING? Since they have NOT considered the solar energy that would OTHERWISE be REFLECTED back into space, without THAT CALCULATION, it is SCIENTIFICALLY IMPOSSIBLE to state that EVs DECREASE GLOBAL WARMING. IMPOSSIBLE and NOT scientific. ELON. do you get it? you’re NOT much of a scientist.
1.2 There has NEVER been a successful HIV vaccine. Isn’t that interesting? but that’s a HUGE clue to what it means to have an ANTIBODY in the body.
1.3 Our bodies DO create antibodies against the HIV virus. That is one of the ways we actually KNOW someone has been infected with HIV.
1.4 Now, it IS true that we can find HIV antibodies in someone who is infected with HIV, it is an ABSOLUTE FACT.
1.5 Having this HIV antibody in a human body does NOT mean that the HIV antibody helped the human fight off the HIV in ANY way, correct??
1.6 ALL it means to have an HIV antibody in the body is that the body produced an antibody against HIV. that is ALL it means. NOTHING MORE.
1.7 Why would having an antibody against a virus mean that we have protection against that virus?
1.8 Look at measles. we DO form antibodies against the measles virus. so, we have a measles antibody against the measles virus. MERELY having an antibody in our body against a particular virus CLEARLY doesn’t mean that it helped us. look at HIV.
1.9 So, measles versus HIV. we create antibodies against both. for the measles virus, we jumped to the conclusion that MERELY HAVING the measles antibody in our body was protective. but WHY DID WE MAKE THAT ASSUMPTION??
2.0 Why did we make that JUMP to think that having an antibody in our body was HELPFUL? because it IS a jump in logic. clearly we have NEVER been able to make sufficient antibodies against the HIV pathogen to help ANYONE.
2.1 Having an antibody against a virus and MAKING THAT LEAP IN LOGIC to assume that the antibody was useful is CLEARLY DEBUNKED BY the HIV case. we DO form antibodies against HIV. doesn’t help. We have tried to make antibodies to protect against HIV. never worked.
2.2 What IS clear is this. that the viruses that antibodies are supposedly useful against? the body can take care of those viruses like measles having NEVER faced measles, having NO antibodies against measles, and our cells handle the virus within the cell PRETTY EASILY.
2.3 so, did the measles antibody EVER help against measles? how did ANYONE make this LEAP IN LOGIC?? when someone WITHOUT measles antibodies handles measles pretty easily???
2.4 Isn’t it PRETTY clear now? that ANY virus that comes into our body, we WILL form antibodies against? But, why can’t the HIV antibody help prevent HIV? when the measles antibody supposedly helps prevent measles??
2.5 OR MAYBE. INFINITELY MORE LIKELY. we almost ALWAYS heal from measles with ZERO measles antibodies. and we NEVER are protected against HIV even with a TON of HIV antibodies.
2.6 CONCLUSION?? Once viruses ENTER cells, if we don’t have a mechanism of handling the virus WITHIN cells, we are DOOMED (HIV) and if we have a mechanism of handling the virus WITHIN cells (measles), we are FINE.
2.7 And with COVID? an infected cell can create 50,000 copies of itself in ONE cell? and if you don’t stop 99% of viruses, then that ONE virus can replicate like CRAZY?
2.8 and the HALF life of antibodies is ONE month? and EVEN if you were SUCCESSFUL the first month, half the antibodies can NEVER stop 99%?
They made a LEAP in logic when they assumed finding an antibody in our blood against a virus was useful. that was NEVER the battle.
2.9 The battle begins when the virus enters the cell. if we can handle the virus inside our cells, it’s an easy virus for us. if we can’t handle the virus inside our cells (HIV), then we are screwed. The antibody?? not for viruses. for extracellular pathogens.
3.0 that ONE assumption of believing that finding an antibody against a virus in our blood, that it was useful. was an ASSUMPTION. and no science beyond that.
If you, pro vaccine people are so well-informed, take on this bet. I bet you $1 million that the Ribonuclease enzyme destroyed (compared to the COVID antibody) more COVID mRNA within lung alveolar epithelial cells in 2020.
Never mind, I’ll let you off the hook. No bet. The COVID antibody was barely present in 2020. The COVID antibody doesn’t seem to have a path through the lung barrier into the lung alveolar cell area. The lung barrier can stop water molecules that are 18 Daltons in size and the COVID antibody is a gargantuan 145,000 Daltons in size. The lung barrier can stop WATER molecules. This barrier MUST be passed by the COVID antibody in order to reach the lung alveolar cells. But, this barrier WILL stop the COVID antibody.
And EVEN if the antibody CAN somehow get through the lung barrier, the antibody doesn’t enter lung alveolar cells. And that IS where the COVID viral RNA inserts itself.
And EVEN if the antibody DOES somehow make it through the lung barrier and somehow DOES enter lung alveolar cells, the COVID antibody does NOT bind to COVID viral RNA inside lung cells.
And EVEN if the antibody DOES somehow make it through the lung barrier and DOES somehow make it into lung alveolar cells and DOES somehow bind the COVID viral RNA inside lung cells, the COVID antibody ONLY touches molecules. It does NOT destroy without the help of T-cells which are OUTSIDE the lung cell.
It’s a simple question. If someone had COVID-19 antibodies in the year 2020, how did they form those antibodies in their blood? Wasn’t there only ONE way? To actually have the COVID infection and wait a couple of weeks?
Then that means BEFORE that person had COVID-19 antibodies in their blood, the ONLY way to have formed those COVID-19 antibodies in their blood was actually having a COVID infection and waiting for two weeks. Well almost EVERYONE in 2020 who got COVID got better within a week to 10 days. NO COVID ANTIBODY in sight while most people recovered from COVID in the year 2020.
It is an ABSOLUTE fact that anyone who got COVID for the first time before 2021 when the vaccine came out, that NOT ONE PERSON had a COVID antibody in their body for the first week or so of their FIRST Covid experience.
I am saying that if we fought off the virus with RNases in the year 2020 and 99% of us survived and a much higher survival rate in the young, KNOWING what the human body did to help us recover from COVID is the ONLY way to assist the human body do what it did so well. and the human body used RNase enzymes. It did NOT use COVID antibodies in the year 2020. The COVID antibody was NOT even present!
And almost everyone on earth knows about the COVID antibody that did practically NOTHING in the year 2020 and the RNase enzyme saved humanity and NO ONE knows about it???? BECAUSE OF THE DEMOCRAT’S POLICY OF CENSORSHIP.
Or practically no one. and my discovery? That fasting activates MORE RNase enzymes. And fasting is SOOO effective that there isn’t a point to vaccinating ANYONE. because RNases enabled more than 99% of us to recover with NO COVID ANTIBODY and further activating MORE RNases will take that well past the 99% survival rate. So fasting will be INFINITELY more useful than any COVID vaccines.
The ONLY way to HELP the body do what it did SO amazingly well in the year 2020 to help 99% of us survive COVID? The ONLY way to help? KNOW what the human body did. And it did NOT use COVID antibodies. The human body used RNases to destroy the COVID viral RNA strands within lung cells. NO OTHER SCIENTIST EVEN HAS ANOTHER SUGGESTION AS TO HOW VIRAL RNA WITHIN LUNG CELLS IS DESTROYED.
If you understand risk/benefit, when there is no benefit the risk/benefit ratio shoots through the roof. The COVID antibody has no path through the lung barrier. The hypothesis of the COVID vaccine and how it provides benefit should not be a secret should it?
Do you see why you would have lost the $1 million bet vaccine lover? Your beloved COVID antibody? It’s just a fish. The red herring variety. You got fooled. The COVID antibody had no role in our recovery from COVID in 2020. Or in 2021. Or now. You got played for a fool.
And THIS ridiculousness? Is what you vaxxers were SO intent on making sure everyone GOT? And if they didn’t get it, you HAPPILY fired them? And all you vaxxers did the JOHN OLIVER thing and made FUN of the anti-vaxxers? with THIS SHYYYT???? lol. Whose the dumb one??????
1.2 A growing embryo is an extremely delicate situation. In an adult, an infection in a finger results in ONLY damage to the finger. In a growing embryo, an infection or damage to ONE cell has repercussions to ALL future cells emanating from THAT cell, it could be a WHOLE arm
1.3 The more QUIET the environment during growth of the embryo during the first trimester, the SAFER and LESS risk of abnormalities.
1.4 This quiet envirornment is SOO critical during the early phases of growth (since every cell creates a DOWNSTREAM lineage of cells that are all DIFFERENT) that it is VERY common for pregnant women to very commonly have severe nausea/vomiting in the first half of pregnancy.
1.5 It is BETTER for the pregnant women NOT to eat or eat VERY little and only want VERY simple foods (crackers/rice), even if this may mean weight loss for the pregnant mother. The more SIMPLE the components in the pregnant mother’s BLOOD, the SAFER for the developing embryo.
1.6 Evolution almost ALWAYS gets it right. those pregnant women who ATE WELL and ATE DIVERSE foods during the first half of pregnancy were LESS likely to delivery a healthy infant.
1.7 Have you noticed that you can EVEN smell the COFFEE you drink in your urine? aromatic compounds from the COFFEE make it into the pregnant mother’s blood which is why you can SMELL it.
1.8 That is how IMPORTANT it is for the pregnant mother’s blood to be AS FREE from unusual molecules as possible. EVEN DIFFERENT molecules from FOOD can be a problem.
1.9 Now, if you give a pregnant mother a VACCINE during her first two trimesters, the number of molecules are formed is an EXTREMELY long list. All these molecules in the mother’s blood can enter the circulatory system of the embryo/fetus.
2.0 There are HUNDREDS of cytokines and chemokines that the body produces in response to mRNA vaccines, which act as a STRONG adjuvant. All these cytokines/chemokines are in the mother’s blood and many are smaller molecules and can enter the blood of the fetus.
2.1 We WILL stop the STUPIDITY that is the vaccination of PREGNANT WOMEN with ANY vaccine. PREGNANT women were our SACRED COWS. And the Directors of the CDC, NIH and FDA that NEVER SPOKE OUT AGAINST the vaccines for pregant women will ALL BE HELD TO ACCOUNT
2.2 This will NEVER BE STUDIED. we will NEVER find out the exact cytokine and chemokine that caused all these issues in pregnant women because we will NEVER vaccinate pregnant women AGAIN in the history of the world. NEVER AGAIN. NOTHING TO BE STUDIED.
I have proof that Dr. Fauci COVERED UP the BIGGEST MEDICAL MISTAKE IN HISTORY.
The COVID antibody has no path into the lung. When I disocovered this, I let Dr. Fauci know. I did run it by my mentor, the Director of Ophtho at Johns Hopkins.
1.2 I couldn’t believe the size of the mistake either and I mulled over it and talked to a lot of people. No one had an answer. Isn’t it ridiculous? The COVID antibody never enters the lung. Wasn’t that the whole point of the vaccine? To help the LUNG in an infection?
1.3 But, finally I wrote the page or two letter, and sent it to Dr. Fauci and several other directors and certified letters to every member in CONGRESS. When I had previously discussed it with my mentor, he listened quietly, and then told me I would be going to Stockholm.
1.4 I really thought that would end the COVID vaccine. This was about two years ago, so before the vaccine approval. But, no. I received a reply from Dr. Emily Erbelding, who thanked for sending the letter to the several directors, including Dr. Fauci.
1.5 But, a few weeks later, when Dr. Erbelding replied, what she generally seemed to say in her email was, well, sorry but our clinical results are awesome and here’s a 1985? paper that will give you more info.
1.6 I was shocked. Didn’t I just tell them that the COVID antibody will never go into the lung? I told my mentor and showed him the email. He was very disappointed and sad that they couldn’t keep an open mind. He said, all they had to do was throw a couple million $ into it
1.7 So, being me. And wordy. But precise and detail oriented. I wrote back a 73 page letter to Dr. Fauci. Explaining every aspect of this huge mistake. No reply. Of course, I sent him email after email. and even Dr. Francis Collins who happens to be the NIH director.
1.8 And Dr. Collins happened to be my genetic professor in medical school (U of M, ann arbor, go blue). No reply. Couldn’t believe it. Just couldn’t. By this time, I knew there was something horribly bad going down.
1.9 I then tried to contact the CDC. I must have emailed at least a couple dozen directors over and over. And I must have called at least half a dozen. The massive mistake is simple, isn’t it? The COVID antibody will never enter the lung.
2.0 The CDC directors, very curt and short and rude to me. Of course, not when I first call. I’m a lasik surgeon trying to give them some important info… and then, easy to explain to CDC M.D.s Blood lung barrier? can stop water? antibodies are huge??
2.1 And then, invariably, their rush to get off the phone, often just click. The coldest shoulders, I got from them. Now, I knew aargh. My highly educated double fellowshipped MIT friend kept telling me, you’ll never stop it.
2.2 This timeline isn’t expanded. I did tons in between every tweet. But, I’m going to fast forward now.
I send ALL my info to Pfizer. 73 pages, 12 pages , 3 pages. All the stuff I’ve been writing. I even explain that the PREP act gives them legal immunity, UNLESS…
2.3 Pfizer, UNLESS you’re involved in WILLFUL MISCONDUCT. How will you explain to mothers later? whose children had severe side effects? Dr. Lee INFORMED you of your HORRIBLE MISTAKE? and you continued to sell your vaccine??
2.4 Pfizer, CEO and directors, do you ALL want to ruin a huge company? For ONE vaccine? Why don’t you just do the right thing?
2.5 Fast forward again. about a week ago, I called Moderna and taped a 25 minute conversation. Explaining all this. that their antibody has no path into the lung, that we had another way of healing, ribonucleases, that there are a lot of questions.
2.6 I told Moderna I would release the tape on twitter. Fast forward. A couple of days ago, big news breaks and its huge on twitter, Pfizer admits did not test for viral transmission.
2.7 Now, current. the day i’m writing these tweets. this is for teaching purposes, purely speculation about different actions organizations or companies can take, from very ethical, to very unethical. it’s hard to know the truth. so, we have to examine every possibility.
2.8 speculation. Now, If I’m Moderna and they thought their vaccine saved the world, and this lasik doc calls up and tells them about this ridiculously HUGE mistake, write under their NOSE, and SO simple EVERYONE can see it, they should have panicked. And then, say.
2.9 speculation. moderna still. They should have said, this guy probably talked to PFizer too. more lawyers, more experienced lawyers. moderna thinks, we need to talk to them. we might be on the same side…. as Pfizer
3.0 again. speculation. but that’s what detectives do, play out different scenarios to find the bad guy, if there IS one. so, don’t SUE me for clearly labelling this SPECULATION. That’s to YOU BIG PHARMA
3.1 speculation. Now, Pfizer. What a bad version of Pfizer might have done. If moderna calls them again, this is a scenario. And moderna says, hey did this lasik doc talk to you guys too? what’s your plan? is this a real issue? Our antibody doesn’t go into the lung?
3.2 speculation again. Pfizer now KNOWS this news will break once the audiotape of the lasik doc and moderna conversation comes out. They need to get ahead of it. so, they KNOW they have to have LEGAL immunity. and KNOWING that they did something willful is the problem.
3.3 speculation STILL. If a bad version of Pfizer only wants to protect themselves, cuz for a year they have known about this HUGE mistake (that’s when the lasik doc told them) and now there is legal liability.
3.4 speculation, so, Then IF Pfizer comes out with this “never tested for viral transmission” which went huge on twitter, then they can say, we didn’t EVER plan to have no viral tranmission, so when this lasik doc says we are involved in willful misconduct…. (continued)
3.4 speculation still. if that doc says we were involved in bad deeds, we can say, we NEVER said the antibody was in the lung. or another way of saying that which they did say, we DID NOT TEST FOR VIRAL TRANSMISSION. So, now even if the Lasik DOC says, you’re doing something bad
3.5 speculation still.. we (PFizer, the bad version) can say, no. we made the vaccine to decrease severe morbidity and mortality. Then, the lasik doc’s claim that we were doing something wrong cuz the antibody isn’t in the lung, doesn’t matter.
3.6 speculation still. Pfizer still (bad version). If we weren’t trying to ever get the antibody into the lung, then when this lasik doc tells us and the world the antibody isn’t in the lung, it doesn’t matter legally for us.
3.7 speculation still. Pfizer (bad version, i’ll get to the good version, but that one is short) then can’t directly say, we never planned to get the antibody in the lung. But, what they CAN say is, “we never tested for viral transmission”. which is the same thing. but clever
3.8 speculation again, no need for lawsuits. detective work requires imagination.
So, NOW the world is upset because Pfizer ADMITS that they “never tested for preventing viral transmission”. BUt, Pfizer gets itself OFF the hook legally. NO ONE told them to test for that
3.9 spec. Pfizer would be off the hook because if I told them something that was a horrible mistake cuz their WHOLE goal was to get the antibody into the lung to protect the lung, but if they can say, that was NEVER our intention, then they didn’t do anyting intentionally wrong
4.0 Spec still. Now Pfizer has clever attorneys and a lot of them. So if this is why they did it, wow. Dirty. But again, i was speculating about the bad version.
So, continuing. Vaccines then. Are ALL vaccines ONLY to prevent SERIOUS issues with the patient only?
4.1 spec still. See, if vaccines are ONLY to prevent serious issues with vaccinated person and NOT to reduce viral transmission, then guess what? Pfizer, in this situation, ALL YOUR VACCINES other than COVID can NOT be mandated. Measles, mumps, rubella, you name it.
4.2 Spec still. Pfizer, if this is what you were thinking, pick and choose. You are playing around with the definition of vaccines so you can escape legal liability? Why did Dr. Emily Erbelding at the NIH responding for Dr. Fauci feel the need to defend antibody in lung?
4.1 But backing up and explaining the stupidity of the COVID vaccine hypothesis.
Our lung is basically a pocket of air. Our body, mostly water. If our lung couldn’t keep water out, we would have drowned in our own fluids. Our lung has this waterproof barrier..
4.2 this waterproof barrier can keep tiny little water molecules weighing only 18 daltons, OUT of our lung.
So, COVID enormous antibody molecules are made in the blood/lymph. to get into our lungs, they have only one option, to pass through our LUNG BARRIER.
4.3 These crazy big COVID antibody molecules weigh 145,000 daltons. If a water molecule looks like a diet coke, covid antibodies are the size of a mini-suv. so, the lung barrier can keep water molecules out and will never let in COVID antibodies into our lung.
4.4 There isn’t a single peer reviewed paper ON EARTH that describes an active transport system that can ferry these hcrazy gargantuan COVID antibodies across the very tight waterproof lung barrier, into the lung.
4.5 Even crazier, in 2020, NOT one person in the US who got COVID for the first time (or anyone else for that matter) had a SINGLE COVID antibody in their system. Millions got COVID and healed within a week to 10 days WITHOUT COVID antibodies.
4.6 To have helped anyone who recovered from COVID in 2020, the COVID antibody would have needed to actually BE there. It wasn’t. To have helped, it would have needed a TIME MACHINE. Per fauci, follow the science? or the science fiction?
4.7 So, the COVID antibody would have needed a time machine to have helped anyone in 2020…. and when the antibody FINALLY arrives late to the party, either naturally or via vaccine, IT CAN’T GET THROUGH THE LUNG BARRIER, or it can. WITH A TELEPORTER. science fauci fiction?
4.8. Very importantly, SOMETHING saved us in 2020, and it was NOT the COVID antibody. So, that SOMETHING, whatever it was, it’s important to KNOW. Because if we know what it WAS, we can FACILITATE IT.
4.9 That SOMETHING that saved us in 2020, I call it the LEE Enzyme (For fun). It’s the ribonuclease enzyme. Why wouldn’t this be it? IT was actually THERE in the year 2020. Not the COVID antibody. It was actually IN our lung cells, NOT the COVID antibody.
5.0. The FUNCTION of a ribonuclease enzyme is to DESTROY RNA, not just OUR RNA, COVID viral RNA TOO, very interestingly, COVID VACCINE RNA TOO. anyone wonder why the COVID mRNA vaccine was FROzen?? Cuz, this LEE ribonuclease.
5.1 Yeah, the mRNA vaccines were FROzen cuz, this “contamination” (what Pfizer and Moderna feel is a CONTAMINATION) chews through ANY RNA. Irony? Pfizer considers this enzyme CONTAMINATION and this enzyme is what SAVED HUMANITY. Scientists are so clueless sometimes.
5.2 So, see? can you trust anything someone says, when they call the REAL HERO a “contamination”? True. The solution to COVID WAS in their vials, it JUST WAS NOT THEIR VACCINE mRNA. You can’t write stuff this crazy. truth is stranger than fiction.
5.3 Now, this LEE enzyme that saved the world from COVID in 2020. Why would it STOP working in 2021 and 2022 and forever in the future? It probably IS the reason why we survived in 2021 and 2022. It probably was NOT the COVID antibody, EVER.
5.4 see how logically the COVID antibody wasn’t the hero? Fauci wanted it to be the hero. Maybe because the path from any VACCINE to MONEY had been vetted MANY times? Well, he should have checked the path from blood into LUNG for the antibody. Follow the Money Much Fauci?
5.5 “but the mrna vaccine clinial trials showed such good results”. ha. Can we clearly say it was NOT the antibody that can’t enter the lung? maybe.. it was the SIDE EFFECT of the vaccine, tricking the body into making chemokines and interferon, giving us muscle aches?
5.6 So, told money fauci, repeat the clinial trial. Compare the COVID mRNA vaccine to the FLU vaccine. What? why? flu vaccine doesn’t make a covid antibody. It DOES ALSO have the main similar side effects of muscle aches and tricking the body into making chemokines.
5.7 If the FLU vaccine ALSO works just as well as the COVID vaccine, against COVID… hmmm. just maybe the side effects of tricking the body into producing interferon (anti viral by the way), is what resulted in the good results??? (even tetanus shots protect againt COVID).
5.8. So then, the COVID vaccine works, very temporarily, AS A MEDICINE??? IT’s NOT then a VACCINE? Cuz the reason why it’s working is the induction of chemokines by the BODY? holy cow. Then, should you REALLY give people a Medicine when they don’t have the illness??? hmmmm.
5.9. I guess? you can’t mandate a “medicine” when you don’t have the illness? silly scientists. can’t keep their definitions straight. and .. once people start re-defining.. you know, they’re lying.
6.0 that was just a side trip for all the idiots who want to say “the vaccine works, who cares how it works”. yeah, well, in science, IT DOES MATTER HOW SOMETHING WORKS. THat is almost the DEFINiTION OF SCIENCE.
6.1 Back to what saved us in 2020. The ribonuclease. The SECRET and the CURE is HOW to activate this enzyme to destroy RNA. FASTING. Fasting activates this ribonuclease and ACTIVATES MORE of these ribonuclease enzymes. FASTING FOR TWO DAYS IS THE CURE.
6.2 In layman’s terms. Viruses do NOT grow on their own. They grow within OUR cells and when OUR cells are growing more slowly during fasting, guess what? the virus grows much more slowly and our cells are less sick, we cough out less virus and pandemic over.
6.3 Here is the biochemistry behind it. Fasting increases reactive oxygen species, which oxidizes 6 sulfhyrdryl groups on the ribonuclease inhibitor, that then releases the ribonuclease which is extremely efficient at destroying RNA.
6.4 The anti-vaxxers were right (of course, any time someone wants to poke the boundary between nonself and self, your skin, tell them to fuck off), their instincts were spot on. The pro vaxxers? their uppity logic, “any bit of good is good”, pure stupidity.
6.5 So, on a positive note (for now), your elderly relatives and at risk friends, can worry a LOT less. Stupid masks, STOP the virus from replicating AT the source. FASTING FOR TWO DAYS. Just know, when infected with COVID, next two days, FOOD CAN KILL YOU.
6.6 I’ve been cancelled everywhere online before. I really can’t believe I’m not cancelled yet on twitter. My comments wouldn’t show up on doximity. On FB, comments gone in a day. My lasik forums, cancelled me. LinkedIn, said I’m gone for life. So, can we do this fast?
Re: Fatal flaw with the COVID vaccine hypothesis and possible lack of LEGAL IMMUNITY for the California Medical Board if “willful misconduct” is engaged in.
To: California Medical Board, Chief Legal Counsel
Dear Mr. Aaron Bone,
The issue is much bigger than that, I’m afraid. You told me in your email that I am responding to,
“The bill only impacts the dissemination of mis/disinformation from the licensee to a patient under the licensee’s care in the form of treatment or advice.”
I have little fear that the California Medical Board will EVER try to take my license away or punish me. Today, I spoke to a lasik consultation and asked her, “how does the COVID antibody enter the lung air space”? I asked her dozens of questions that show the stupidity of the COVID vaccine hypothesis as it stands right now. She turned out to be an anti-vaxxer who was extremely happy to hear my very scientific questions that illuminate the STUPIDITY that is the COVID vaccine hypothesis. Her mother informed me that based on my questions that she had NEVER heard before, she would NOT take her THIRD COVID vaccine booster. So, Mr. Aaron Bone, were my questions that DESTROY the COVID vaccine hypothesis of a neutralizing antibody in the lung that binds COVID before the virus can infect a lung cell, were my questions “disinformation”??????? You don’t know science. You are in NO position to explain to the general public or to PHYSICIANS what I can or cannot say or can or cannot ask to a patient.
Many in your staff got a 20 minute lecture from me, explaing the stupidity of the current COVID vaccine hypothesis. They were in SHOCK. The reason why you have all those copies of my letter to Gavin Newsome and reminders to reach out to me IS because they BELIEVE the information I present to them and they now KNOW that the COVID vaccine is pure stupidity at its finest. THE COVID VACCINE HYPOTHESIS IS THE SINGLE BIGGEST MISTAKE IN THE HISTORY OF MEDICINE. Your staff EASILY understood it. Now, put your pride aside and do the right thing. Otherwise, it will be very financially costly for the State of California and very possibly for your personally. I will explain below.
The government gave any organization involved with the COVID vaccine legal immunity, but with a significant exception that is included in the PREP act. The significant exception to immunity available in the PREP ACT is for “willful misconduct”, an intentional act or omission to achieve a wrongful purpose. Whether your institution engaged in willful misconduct resulting in the loss of available legal immunity is likely to be subject to a factual dispute during litigation.
I have found the fatal flaw with the COVID vaccine hypothesis. Every organization that I have reached out to and informed of this nightmare error, is committing “willful misconduct” if the organization continues to INTENTIONALLY PROMOTE the COVID vaccine to unsuspecting members of the general public who then receive this COVID vaccine.
If the organization engages in a willful act of OMISSION and fails to inform its constituent members of the information I am providing you, the fatal flaw with the COVID vaccine hypothesis, then the organization ALSO is involved in “willful misconduct”
The information I will provide you is shocking. The COVID antibody has NO path into the lung air space. There isn’t a SINGLE peer reviewed paper on earth that describes an active transport mechanism that can move gargantuan COVID antibodies (with a molecular weight of 145,000 Daltons) across the lung barrier (which can prevent water molecules of 18 Daltons from filling our lung air space) into the lung air space which is where COVID is destroying lung cells.
The burden of proof is NOT on me to show that such a paper does NOT exist. The burden of proof is on THOSE who support the COVID vaccine science to provide a paper that SHOWS HOW the antibody that is 8000 times heavier than a water molecule can traverse the lung barrier which can stop water molecules. NO ONE HAS PROVIDED A PAPER LIKE THAT TO ME BECAUSE IT DOES NOT EXIST.
I have performed 80,000 lasik surgeries in California since 1998. I have had ONLY one complaint in all my years of being in California, by a patient I REFUSED to do an elective lasik surgery for. At the time, when I called the California Medical Board, the agent told me, physicians accidentally KILL patients and I refused to do an elective surgery that she could go anywhere and have performed and he laughed at how silly it was. I have NOT had a single lasik lawsuit, arbitration, or claim against me since I started my three offices. I had ONE in fellowship that his expert witness felt he should drop. I AM ONE OF THE GOOD GUYS. I’ve done lasik for many employees who work at YOUR California Bar. I know Russ Weiner, a past chief prosecutor at the California Bar, PERSONALLY. As an aside, do you think lawyers would want ME, a physician to be PRESIDENT or CHIEF prosecutor of THEIR BAR? So, why would physicians want an attorney to be president of OUR Medical Board?????
I performed my lasik fellowship at USC/Doheny in 1998, under Dr. Peter McDonnell, who is currently the Director of Ophthalmology at Johns Hopkins Medical School. He has been chief editor of Ophthalmology Times for at least 15 years and there isn’t an ophthalmologist on earth who doesn’t know who he is. He is known for his academic research and especially for his integrity. When I told him about my findings, he was aghast. Our first conversation about this, around two years ago, after 30 minutes of me explaining, his words to me, “Joe, you’re going to be going to Stockholm”. We have talked at least a dozen times these past two years about my findings and during our last conversation, he told me, half kiddingly, “Joe based on this cancel culture environment, I think the government is going to try to put you in prison, and I’ll fly out from Baltimore and bail you out, cuz your daughter needs her father”.
It is the moral, ethical and legal duty of the California Medical Board to inform all physicians in California that the COVID vaccine hypothesis may be fatally flawed and that scientists will have to review the information that I present, scientists must form a NEW hypothesis and then scientists MUST re-submit an FDA application for approval UNDER the NEW hypothesis. This is how science works. Mr. Aaron Bone, you do NOT have to agree with my findings.
You JUST have to acknowledge as ANY REASONABLE PERSON WOULD, that an extremely serious issue with the COVID vaccine hypothesis has been brought to your attention and it MUST be discussed by scientists at the highest levels and prospective patients MUST be informed of this issue to have valid INFORMED CONSENT. Remember what a mother of a child who receives a vaccine and later has severe side effects, remember what THAT mother will say, “Mr. Bone, did I hear this right? Dr. Lee brought this nightmare issue to your attention, and you JUST sat on it???? and you let MY child be vaccinated when he informed YOU that there WAS no path for the antibody into my son’s lung? and that he showed you there WAS no paper on earth that shows HOW the antibody DOES go into the lung? and yet you just SAT on this information and LET my son be vaccinated?”
You see Mr. Bone? Withholding information of this magnitude WILL be seen by any reasonable jury as “WILLFUL MISCONDUCT”. In science, when I raise a question of this magnitude of such a fundamental issue (“well, get the vaccine but we have no idea how it enters the lung”) THERE MUST BE AN ANSWER. If there is no answer in writing, IT IS NOT SCIENCE. IT IS HORSE SHIT.
There is NO downside to you PERSONALLY for doing the right thing with this information and putting out a press release ASAP to disclose the nightmare oversight by the FDA and NIH and CDC in not vetting HOW the antibody enters the lung space. There IS a downside to the California Medical Board for NOT reporting this to all its constiuent members and to the State of California COVID response team via the “willful misconduct” by omission. Also, there WILL be personal consequences to you if I am shown to be correct (and I am) since the California State may be subject to several class action lawsuits, since the Legal Immunity clause has a major exception of “will misconduct” by action OR OMISSION. Do you really think that everyone will say, let’s just forgive Mr. Bone for making a mistake? Really?
Mr. Aaron Bone, make time to have a zoom meeting with me this Monday. There is NOTHING you can do or have done in your life that is more important than this issue, so far as HEALTH of the general public AND FINANCIAL CONSEQUENCES FOR THE STATE (possibly yourself) and trying to bury this information that shows the stupidity of the COVID vaccine hypothesis will only result in digging a deeper and deeper hole for the California Medical Board. The President of MY Medical Board is an attorney? Listening to HER on this issue is not wise. She Is already on the wrong side of this issue and she has a major conflict of interest issue since her personal reputation will be impacted, since she helped support the STUPID 2098 bill. I have already reached out to all the physicians on this board. Present this letter to them also. The President should EXCUSE herself from this decision as she already hates me and she is hugely biased as she knows I don’t believe that an attorney should be the president of MY MEDICAL BOARD. Also, there is another idiot on the board whose mother is my father’s friend who should excuse himself from the vote. He hates me too and I think he’s a pure dumbshit korean idiot who I sent all this information to a year ago. I have informed him in the past that I will do everything in my power to get his dumb ass OFF this board, someone who has never gotten an A in even basic general chemistry (me? scored 97 percentile on my boards and gave my LIFE to medicine and science). I will NOT have idiots like that decide MY future if I have ANY say, and you know I will.
If you’re offended by my foul language, I’M OFFENDED AT THE STUPID MEDICAL AND POLITICAL ESTABLISHMENT’S ACTIONS THAT INCLUDE INJECTING INFANTS WITH PURE HORSE SHIT SCIENCE FICTION VACCINES WHEN THEY CAN’T EVEN EXPLAIN HOW THE ANTIBODY ENTERS THE LUNG. My use of french is hurtful? Fucking injections can KILL. My use of french is not professional? Injecting babies with shit that can kill when you don’t know how the antibody even enters the lung (and ALL those who allow this) is infinitely MORE unprofessional.
The signs are multiplying that the US and Israel are headed for some sort of mega black swan event. The result will be that both countries cease to exist in their present format. That is because the Federal Reserve Board -the fountain of power for the Satanists- is on the verge of collapse. If it goes, then everything under it, such as the UNITED STATES OF AMERICA CORPORATION, the BIS, the World Bank, the IMF, the UN and 90% of the world’s transnational corporations will also collapse and come under new management.
The signs of FRB collapse are manifold. As we have previously noted, the FRB interest rate of 5.25% has mathematically doomed at least half of all US Banks because it has devalued all the zero or close to zero interest stuff on their books. The FRB is now resorting to fraudulent accounting to hide the resulting bank run.
This was seen when deposits at most of the big US banks (owners of the FRB) were “delayed” by the FRBs Automated Clearing House (ACH), network.
This apparently allowed the FRB to use “seasonal adjustment” fakery to turn a $33 billion deposit outflow (bank run) into a $52 billion inflow. This trickery has magically boosted deposits by $168 billion since April. Since FRB rules allow 1000 times leverage, these fake deposits back $168 trillion worth of “financial instruments.” In other words, the whole financial house of cards rests on a foundation of fraud.
The US banks are also now stealing people’s money outright as well. Many bank customers are getting letters saying all of their checking and savings accounts are being closed. The explanation, if there is one, is something like “Per your account agreement, we can close your account for any reason at any time.”
This is happening in Australia and other KM-controlled countries as well.
The KM are also now pushing desperately to outlaw cash and force us into a digital prison. The new FedNow inter-banking communication system is “possibly unconstitutional” and “threatens the very freedoms that all liberty-loving American citizens should hold dear,” says Bitcoin Magazine Editor Mark Goodwin in response to an FRB attempt to silence his publications’ criticism of this system.
These moves are connected to the upcoming November 15th deadline for the US government to “raise the debt limit.” We are hearing the Chinese and other creditors to the US are determined not to let the US “government” circus show continue any longer.
This financial trouble is why a political or military-type mega black swan event is probable. In the past, the FRB has responded to crises of this nature with events like 911, Fukushima and most recently the pandemic and vaccine global genocide attempt.
One possibility is some sort of holocaust or mass sacrifice to Satan is being planned for Israel. We are getting credible reports from foreign diplomats based there that large portions of the country have been evacuated to Ukraine. These coincide with reports from Russia that roadblocks have been set up in the Ukraine and only people who can prove they are Jewish are being allowed past them.
Mossad sources further claim Israel as a corporation has expired on October 31st. Also, China has removed Israel from its maps.
In response, Netanyahu has appeared showing a map of Israel minus the Gaza strip. The last thing left for Israel to do is wage a Great War.
“Israel is a global terrorist organization. That’s exactly what they are, but It is better to refer to them as the cancer of planet Earth,” a Mossad source says.
In another sign Jews still in Israel are being prepared for another Holocaust, Satanic thugs in Israel are violently attacking genuine Jews who are protesting the genocidal acts of their government.
According to MI6, the people behind this are Crime Minister Benyamin Netanyahu and “a group of extremist Israeli nationalists who assassinated various international characters over the years including a Swedish count by all accounts so to speak and also had a go at a certain Mr. Winston Churchill back in the day. They style their vision of a modern Israel on the fascist states of Spain, Italy and Germany…The joint Israel and Gaza Strip incursions are indeed a slaughterhouse of blood sacrifice and now genocide. Left unchecked they will level the entire place to the ground and all in it.”
Netanyahu himself refers to his Jewish and Palestinian enemies as Amalek:
“The Lord ordered King Saul to destroy the enemy and all his people: ‘Now go and defeat Amalek and destroy all that he has; and give him no mercy: but put to death both Husband and wife; from youth to infant; from ox to sheep; from camel to donkey.” Book of Samuel 15:3.
Heritage Minister Amichai Eliyahu agrees saying “One of Israel’s options in the war in Gaza is to drop a nuclear bomb on the strip,”
In a sign they know something is about to happen there, the Pentagon will no longer allow its senior military leaders to travel to Israel and will discourage members of Congress from making trips. “Israel will not recover from this mistake,” a senior CIA source warns.
In other words, unless action is taken, the KM are about to stage a murder-suicide of Israel rather than accept Jewish liberation from millennia of Satanic control.
Turkey might step in by reasserting control over Israel. “It is Türkiye’s duty to stop the bloodshed in Gaza,” President Recep Erdogan said on Sunday. “We are doing and will continue to do more than what is visible,” he said implying NATO’s largest army might intervene.
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