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Beaux Reliosis Profile picture
@BeauxReliosis
May 8 • 4 tweets • 3 min read Twitter logo Read on Twitter
Some of the “data” MarDx provided in their IgM Western blot application to the FDA. (MarDx WBs were 1st to be cleared after infamous #Dearborn conference.) A few interesting tidbits in here.

#LymeDisease #FOIA Image
My favorite: For their sensitivity study, MarDx included specimens of physician-diagnosed cases “relative to #LymeDisease case definition.” These undoubtedly would have been pre-screened arthritis samples from the Triangle of Death, Steere/Wormser/Dattwyler.
#LymeDisease Image
I can’t even imagine anyone today getting away with using “physician-diagnosed” samples to validate a #LymeDisease diagnostic device’s sensitivity. The crooks would surely protest. I’ve looked @ a lot of 510Ks & have never seen this before.
Another observation of this table: CDC/IDSA say any + IgM after 30 days is a false positive. 198 of MarDx’s 427 positive specimens were positive *after* a month, including 58 that had + IgM for YEARS.

#LymeDisease #ManipulatedDiagnostics Image

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More from @BeauxReliosis

Beaux Reliosis Profile picture
May 8
It might be shocking to people to learn that the original #LymeDisease vaccine, #LYMErix, was so bad & the diagnostic tests so inaccurate, that the surveillance case definition of #Lyme was changed to make them both seem effective. Not a theory; the FDA devoted a whole meeting. Image
It’s probably most shocking to the people who got LYMErix & experienced AEs, & people with #LymeDisease who have been tortured for years or decades without treatment because the “experts” who were in on the scam still control the dialogue to this day.
They’ve trained a whole new crop of gullible, easily indoctrinated, sadistic egoists to carry on for them. Any #LymeDisease “experts” coming out of Yale, UConn, Harvard, NYMC, Hopkins, Stonybrook, UMinn should all be treated with a healthy dose of skepticism.
Read 7 tweets
Beaux Reliosis Profile picture
May 1
🧵
#LymeDisease awareness.

Oh, the things I’ve become aware of, in the last 10 years. TEN years? How time flies when you’re learning something new every single day.

I learned: Image
• The government recognizes only one secondary immune deficiency disease, and it’s not Lyme.

• Yes, “chronic Lyme” can be a condition of immune deficiency.

#LymeDiseaseAwareness
• There is only one nonprofit fighting to fix the root of the problem, and I had to start it myself.

truthcures.org

#LymeDiseaseAwareness
Read 10 tweets
Beaux Reliosis Profile picture
Apr 30
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.

ncbi.nlm.nih.gov/pmc/articles/P… Image
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.
Read 11 tweets
Beaux Reliosis Profile picture
Apr 5
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
🧵🪡
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.
Read 11 tweets
Beaux Reliosis Profile picture
Apr 2
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.

nejm.org/doi/full/10.10…
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.
Read 10 tweets
Beaux Reliosis Profile picture
Mar 11
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.
Read 8 tweets

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