Alan Barbour is an old-school bioweapons scientist who made his name with #LymeDisease. He was studying spirochetes at NIAID’s Rocky Mtn Labs before Lyme was named Borrelia burgdorferi, for his colleague Willy.
This is the “Barbour” from “Barbour-Stoenner-Kelly (BSK) medium,” a medium they developed to more effectively culture spirochetes. He also owned the original patent for recombinant OspA, the antigen in the original #LymeDisease “vaccine” and the new one being developed by Pfizer.
For the record, OspA is not a vaccine, does not induce immunity, and is a *cause* of #LymeDisease. Barbour knew all that but licensed his patent to SmithKline & Yale anyway, resulting in the failed #LYMErix which harmed many people before it’s withdrawal after 3 years.
How did Barbour know OspA injection cannot create immunity to #LymeDisease? For one thing, he points out in this Jan 1982 report that exposure of Borrelia hermsii to penicillin caused the spirochetes to secrete a massive amount of “blebs” which are covered in OspA & other Osps.
See those little blobs? Those are blebs (sometimes called exosomes) that contain spirochetal genetic material. There are also round forms here that can morph into viable spirochetes. These are all covered in hundreds of different antigens, of which OspA is just one.
Spirochetes have many immune-evasion capabilities. One is to change form, only to re-emerge & wreak havoc later. Another is to change which Osps are expressed depending on the environment. They do that by blebbing. They sense a threat, shed their outer surface & express new Osps.
As a side note, in his Jan 1982 report, Barbour noted that this massive shedding of antigenic material after antibiotic treatment could be a cause of the Jarisch-Herxheimer reaction. My mentor, @KMDickson, likened it to throwing fertilizer onto spirochetes.
Barbour knew that injecting OspA into humans could not vaccinate them against #LymeDisease because borrelia are moving targets. Antibodies against a single antigen that the bug may not even be expressing when injected by tick, don’t stand a chance.
Another important finding in this report is that it only takes one or two spirochetes to cause disease.
Since @US_FDA is dragging their feet posting my comments to regulations.gov/docket/FDA-202… “Early Lyme Disease as Manifested by Erythema Migrans: Developing Drugs for Treatment; Draft Guidance for Industry” here you go. #LymeDisease
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Breaking News: The incidence of #LymeDisease erythema migrans (🎯) rash is overstated by more than 10X.
This is done by sleight of hand in calculation method and reliance on the public to infer that the calculation is based on @CDCgov’s estimate of 476,000 cases per year.
Here are the last 2 pages of my document. The #LymeDisease “authorities” want the public to believe the 🎯 rash appears in 70%-80% of nearly half a million cases/year. In reality, the figure is calculated on *confirmed* cases, only about 45,000 in 2020.
A common myth about #LymeDisease is that serological tests work better after 3 weeks of infection because antibodies develop slowly. This is true for only about 15% of cases—those who have the HLAs needed to produce a strong & broad immune response.
Notice the date: 1990. CDC’s #LymeDisease group knew this when they manipulated the case definition a few years later. They implemented a diagnostic scheme that only IDs that minority of highly seropositive cases.
That means #LymeDisease tests are *only* very accurate (especially after a few weeks) if #Lyme = a genetic predisposition to a strong immune response against Borrelia antigens.
Some of the people with whom I interact here on twitland know me very well. For those who don’t, busting the #LymeDisease#mafia has become my life’s mission. I have been sick from a tick bite since 1995. I went undiagnosed for 14 years.
I passed #LymeDisease#borreliosis to my daughter in utero. She is a brilliant, shining light in this dark, corrupt world. When I started advocating for #Lyme victims I thought I was saving her. Turns out she has saved me by giving me a purpose.
I do not have a science background. I hated science in high school. I had to learn everything I know about #LymeDisease along the way. I did much of this publicly on Facebook for several years, sharing what I was learning with others who wanted to know the truth.
When @TruthCuresLyme met with @US_FDA investigators in Oct 2021, it was a hybrid in-person/virtual meeting conducted on their premises and with their virtual meeting platform. Our attorney and a well-known clinician participated virtually. #LymeDisease
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We were on premises for 3 hours with 2 investigators & an administrative employee. We were told of only one other FDA employee participating virtually. However, something very telling happened prior to the meeting. #LymeDisease
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The virtual meeting invitation they sent was rescinded and replaced, causing confusion for our remote representatives. The new invitation included only their names. The old one contained the names of about 10 other FDA employees. #LymeDisease
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The establishment creates this problem by first denying the disease, creating a vacuum that quickly fills up with untested treatments & questionable cures. Then they go about trashing their victims who desperately need relief, and the doctors who are willing to treat. #BTDT#Lyme
It is both infuriating & heart wrenching to watch this scene play out again, with some of the same establishment players engaging in narrative control. Go to ~48:00 for IDSA creep Paul Auwaerter’s word salad tossed at Congress, thx to my friend @PowerOfNeooversight.house.gov/hearing/invest…
That they have denied, conflated & confused for DECADES #LymeDisease#ME#mecfs#cfs#fibromyalgia and passed them off as psychiatric, and now are doing the same with #LongCovid, should tell you all you need to know about #PublicHealth’s intentions.