
THREAD: Women and "Unexplained" Diseases
It's interesting that even a condition as common as #Migraine is still not well understood.
Significant overlap with many other conditions mostly impacting women that are also "not well understood" is present.
https://t.co/EhrnxfItsm https://t.co/R7QUKrZvhR


cc: @jenbrea @ahandvanish @AthenaAkrami @Dr2NisreenAlwan @MBVanElzakker
https://t.co/ITrLBkc3uE
If you work on #longCOVID and say \u201cI\u2019m not an #MECFS expert, I don\u2019t know anything about it, it\u2019s not my job to know about ME or \u2019fatigue\u2019\u201d then you really, REALLY need to learn about ME. This is what MANY infections can do, not just SARS2. pic.twitter.com/zke0MqwrEd
— Jennifer Brea\U0001f992 (@jenbrea) January 14, 2021
Example stats ME/CFS:
https://t.co/GKQqqtWTI7
In ME/CFS is about 80/20 female/male. Before puberty, gender ratio is 50/50. Many anecdotal reports of trans people who take hormones: F to M improve, M to F experience worsening symptoms. Female preponderance is found in both sporadic cases and historically, in outbreaks.
— Jennifer Brea\U0001f992 (@jenbrea) January 12, 2021
Majority of patients with PNES are women, outnumbering men by a ratio of 3:1. Female sex preponderance occurs after puberty & usually before the age of 55
Lack of data does not equal lack of EXISTENCE of a problem, it equals lack of UNDERSTANDING of the problem.
And this problem is immense.
https://t.co/TnF2j4dKs3
Like this tweet if:
— Dr. Jessica Taylor (@DrJessTaylor) January 13, 2021
- You are a woman
- You have ever been ignored, gaslit, accused of exaggerating or told its all in your head by a doctor when you sought help for a medical problem
I just wanna see something.
My optimistic hope is that the enormous amounts of funding for #COVID19 open doors to understanding pathophysiology of previously neglected diseases particularly in women.
But our scientific ignorance should not be wielded to blame & further abuse patients.
Our lack of understanding is not their failure but ours.
https://t.co/LwN8qc0Q4a
Well, it would be so much easier if we didn\u2019t continuously \u201ccarve diagnoses out of the psychosomatic wastebasket\u201d as Maya Dusenbury so eloquently wrote in her book Doing Harm. So I will continue to rant about it. Wont make the medical profession happy, but time to face reality... pic.twitter.com/iFJudV9BLX
— GinaMcGalliard \U0001f9dc\U0001f3fb\u200d\u2640\ufe0f\U0001f315\U0001f339 (@GinaMcGalliard) January 12, 2021
There are more specific, more scientific, and less offensive terminology we can use for women's bodies.
@VirusesImmunity @angie_rasmussen @DocElovitz
To read more of my Threads, please check out: https://t.co/UMdZvE2tDj
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Further Examination of the Motif near PRRA Reveals Close Structural Similarity to the SEB Superantigen as well as Sequence Similarities to Neurotoxins and a Viral SAg.
The insertion PRRA together with 7 sequentially preceding residues & succeeding R685 (conserved in β-CoVs) form a motif, Y674QTQTNSPRRAR685, homologous to those of neurotoxins from Ophiophagus (cobra) and Bungarus genera, as well as neurotoxin-like regions from three RABV strains
(20) (Fig. 2D). We further noticed that the same segment bears close similarity to the HIV-1 glycoprotein gp120 SAg motif F164 to V174.
https://t.co/EwwJOSa8RK

In (B), the segment S680PPRAR685 including the PRRA insert and highly conserved cleavage site *R685* is shown in van der Waals representation (black labels) and nearby CDR residues of the TCRVβ domain are labeled in blue/white
https://t.co/BsY8BAIzDa

Sequence Identity %
https://t.co/BsY8BAIzDa
Y674 - QTQTNSPRRA - R685
Similar to neurotoxins from Ophiophagus (cobra) & Bungarus genera & neurotoxin-like regions from three RABV strains
T678 - NSPRRA- R685
Superantigenic core, consistently aligned against bacterial or viral SAgs
