Beaux Reliosis Profile picture
Apr 5 11 tweets 8 min read Twitter logo Read on Twitter
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regulations.gov/docket/FDA-202… “Early Lyme Disease as Manifested by Erythema Migrans: Developing Drugs for Treatment; Draft Guidance for Industry” here you go.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.
How are #LymeDisease cases confirmed? Either through lab testing (usually the bogus 2-tier serology method) or by ***diagnosis of an EM rash***

It’s a circular reference, just like the @CDCgov #Lyme serum repository.
This #LymeDisease scam has been under our noses for a decade, as @CDCgov finally admitted in 2013 that cases are 10-12X higher than actually reported.

Look:
CDC says 476,000 cases/yr
Only 45,000 met reporting criteria in 2020
Difference: 431,000
Incidence of #LymeDisease EM 🎯 rash CANNOT be 70% of 476,000 because that would be far more than the 45,000 reported cases, for which the criteria *require* either EM rash or lab test confirmation.

Real incidence based on @CDCgov figures = 6.6%

😱
If there were more EM🎯 cases among the other 431,000 they would have been reported as per @CDCgov #LymeDisease surveillance criteria.

Gov agencies, public health “authorities” & self-proclaimed experts have propagated a massively distorted narrative about the #Lyme rash.
They have created a false sense of security among the public, promoting the lie that most #LymeDisease cases will get a 🎯 rash. People need to know that the rash is rare & they could get #Lyme without any cutaneous signs at all.
When I started composing my comment for this @US_FDA docket on treatment for #LymeDisease presenting w/ EM🎯 rash, I was going to rely on the usual reports that can go as low as around 40% & say “not a good idea to base a treatment trial on so few cases.”
I quickly realized that the widely propagated figure of 70% EM 🎯 rash incidence in #LymeDisease was impossible because those cases are required to be reported to @CDCgov. Cases reported in 2020: 45,000. That’s nowhere near 70% of 476,000.
I should point out that the ~45,000 figure is from a CDC source of “provisional” data that has been scrubbed. Their actual # of reported confirmed & probable cases is much lower, which only makes our case stronger.

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More from @BeauxReliosis

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
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
Mar 11
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
1/
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
2/
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
3/
Read 16 tweets
Mar 9
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 @PowerOfNeo oversight.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.
Read 4 tweets
Mar 8
One thing about the failed #LymeDisease #vaccine#LYMErix—that has always been sort of a mystery is what the heck SmithKline @GSK meant by “definite #Lyme disease” and “asymptomatic infections,” the latter of which they claimed their 💉was 💯effective against. 🤔
I mean…

“If you are one of the few people at risk of having zero symptoms from #LymeDisease infection, take our #vaccine to make sure you are 100% protected from an illness you wouldn’t have known you had, if you had it!”

Quite the sales pitch.
I just happened to be skimming some of my #LymeDisease library and noticed this blurb from the October 1997 ACIP meeting.

“In year 2, there were 13 cases of asymptomatic seroconversion, all in the placebo group, for a #vaccine efficacy of 100%”

🤦‍♀️
#LYMErix
Read 15 tweets
Mar 8
Currently @pfizer is injecting 1000s of unsuspecting victims with their #LymeDisease product that definitely isn’t a #vaccine. Bacterial lipoproteins don’t confer immunity & #Lyme spirochetes are a moving target. This 🧵contains stories from victims of the prior vax, #LYMErix.
“Patients are suffering because doctors don’t want to deal with Lyme let alone the vaccine.”

Real patient stories submitted to @US_FDA after #LYMErix injuries. @pfizer is trialing a near duplicate #LymeDisease product right now. Expect similar horror stories.
“I am able to live at home *only with support * from family and friends, and a paid nighttime caregiver.”
#LYMErix victim
@pfizer is looking to cause more of this kind of suffering.
#LymeDisease
Read 18 tweets

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