I read the science. I’ve had ME/CFS since 1989. From bad health to good. Only to be undone by a flu shot in 2016, severely & permanently worsening the disease. New ZealandJoined December 2012
@njfatigue met with Bill Cassidy’s office weeks ago to discuss the urgent need to fund and prioritize #MECFS research. It’s clear that our engagement is breaking through!
This is #NotJustFatigue
David Tuller has battled for us ME/CFS patients for many years. But he can only do it with crowd funding. We are lucky UC Berkeley back his work.
We need David to keep fighting this fight. Donation link in the feed
David Tuller has battled for us ME/CFS patients for many years. But he can only do it with crowd funding. We are lucky UC Berkeley back his work.
We need David to keep fighting this fight. Donation link in the feed
Trump just pardoned crypto firm BitMex for violating money laundering laws — making him potentially the first president in American history to pardon a corporation.
It's truly a new Golden Age for corporate crime.
Last year @TheLancet published an intervention trial for "persistent physical symptoms." Clinically insignificant findings were promoted as a result showing effectiveness. @joan_crawford1 and I responded, and they "rebutted": virology.ws/2025/04/04/tri…
The real story here is the cruel reality of ME/CFS. Severe long covįd has similar effects. They are absolute torture.
The worst of it is the denial sufferers face, the lack of medical expertise or treatments, and likely surge in cases as covįd continues.
1news.co.nz/2025/03/12/i-c…
Unfortunately the pharmaceutical companies can’t see that if one of their drugs helped improve or even cure long Covid or ME/CFS then they would become many times richer than they are already. But for some reason they have the heads in the sand.
cen.acs.org/pharmaceutical…
Great this is getting exposed on a much larger scale. The hard work of many including the epic work of UC Berkeley’s David Tuller who provided Monbiot with much the information in his recent articles.
That work is starting to pay off!!
#MECFS#LongCovid
Great this is getting exposed on a much larger scale. The hard work of many including the epic work of UC Berkeley’s David Tuller who provided Monbiot with much the information in his recent articles.
That work is starting to pay off!!
#MECFS#LongCovid
Why the Left lost. It became so un-fun. Pple got sick of being told what to think, books were edited, opinions were cancelled, except for the Right jocks & their kin. &mobs flocked to them
And then the Right was able to pretend the Left was the Far Left
rnz.co.nz/national/progr…
Microscopic inflammatory processes, possibly involving abnormal microglial activation, fibrinogen deposition, microscopic inflammation & mitochondrial damage = ‘Smouldering MS’
Maybe Prof Ron Davis is right about a ME/CFS subgroup overlapping MS
#MECFSmedscape.com/viewarticle/sm…
886 Followers 6K FollowingStroppy short lefty ginger bird, blessed with various chronic illnesses but still with a sense of humour. Huge Charlatans fan! Also love dogs, goats, donkeys...
5K Followers 3K FollowingProgram Manager of The Covid Recovery Center at Brigham and Women’s Hospital in Boston MA. Opinions are my own. Here to advocate and educate (she/her) 💕
4K Followers 2K FollowingPatient advocating science for #mecfs & #dysautonomia (incl via #longcovid & #postvac).👷🏾♂️Support #neuroscience users & use cases of @MATLAB. Tweets my own.
295 Followers 371 FollowingA Somerset CCC nut in New Jersey.
Bath RFC.
Grumpy old git
All views are strictly my own, or somebody else's
PWME 30 Years. 🐈😽🐟
3K Followers 3K FollowingFounder @LongCovidKids, & wellbeing coach on pause. “Learn from yesterday, live for today, hope for tomorrow. The important thing is not to stop questioning.”
1K Followers 3K FollowingMyalgic Encephalomyelitis (ME) sufferer. Ill since Nov-19. On long term sick trying to keep it together for my family. Just about managing. #ME #POTS #MCAS #LC
3K Followers 4K FollowingThe voice for Long Covid in Ireland. An advocacy group comprised of Long Covid patients fighting for awareness of LC & adequate services in Ire for all patients
969 Followers 2K FollowingStudies @Helsinkisus on hold because of POTS + Long covid / ME. Previously interesting, now mostly into resting. Member of @remissionbiome.
346K Followers 1K FollowingViruses, viruses, viruses and vaccines.
V5=3xancestral+1x bivalent+1xXBB
Professor at the Department of Microbiology
Icahn School of Medicine at Mount Sinai
4K Followers 551 FollowingI am exploring treatments for my daughter's EDS & ME/CFS & implications for people with #EDS, #MECFS, and #LongCOVID. Not an MD or professional scientist.
3K Followers 2K FollowingME/CFS is a connective tissue weakening caused/worsened by a virus. This can lead to Craniocervical Instability, Venous Compressions, CSF leaks and more.
5K Followers 3K FollowingProgram Manager of The Covid Recovery Center at Brigham and Women’s Hospital in Boston MA. Opinions are my own. Here to advocate and educate (she/her) 💕
9K Followers 275 FollowingEx athlete, biker, climber, 1st class biomedicine grad. Entire life lost 2017 post viral ME/CFS. C💉injured 2021 thus turned from pro to anti vax
1K Followers 791 FollowingFormer musician mostly housebound with #ME. BA in Music. BA in Theatre. 3/4 of a MA in Theatre, had to stop due to MECFS. I write. Languages. Genealogy.
2K Followers 393 FollowingSenior Program Director @ScrippsRTI &
#LongCovid patient-researcher @patientled
Let's improve health equity
Accessibility is my love language
Views are mine
11.8M Followers 2K FollowingSen. Sanders of Vermont, Ranking Member of U.S. Senate Committee on Health, Education, Labor & Pensions, longest-serving independent in congressional history.
4K Followers 1K Following#LongCovid since jan’21 ♿️ - tweets with brain fog, so pls bear with me - 📣 tries to advocate @NietHersteld - eager to learn - she/her - tweets in 🇬🇧 & 🇳🇱
180K Followers 915 FollowingProf Operational Research @UCL_CORU, . Member of @independentsage. only posting now at chrischirp at bluesky. https://t.co/nNW5zMenx2
46K Followers 37K FollowingPainting, photography, architecture, graphics, illustrations, sculpture and video. All that is beautiful, attractive, dignified, elegant, gentle, amazing, new
3K Followers 4K FollowingMum to a trans daughter 🏳️⚧️ who loves the natural world.🌿Degrees in Hist/Phil & Counselling/Psychotherapy. Unwell since 2007, worse 2016/17. Improved.🌼
3K Followers 3K FollowingFounder @LongCovidKids, & wellbeing coach on pause. “Learn from yesterday, live for today, hope for tomorrow. The important thing is not to stop questioning.”
493 Followers 502 FollowingPublic health nerd. Public pharma advocate. Health & Economy Fellow @DemocracyCollab. Anti-zionist. MECFS. All opinions my own. 🌹♿️
17K Followers 4K FollowingZoologist. She/her. ME/CFS since 2002, now Severe. Pro-vax but vaccine injured. Life on pause (views my own - unemployed) ♿️ https://t.co/YeMrEWwEg5
1K Followers 74 FollowingThe CREDIBLE destination for everything Long Covid | Dr. Funmi Okunola MD
🩺 Certified CPD/CEU/CME for Licensed Medical Professionals.
Find your answers!
7K Followers 5K Following💙Art, Nature, Books, Some Music. Severe ME 32 years. Daughter severe 38 years. Furious about treatment of ME. https://t.co/gEIrl86Wim
15K Followers 621 FollowingWith ME 36 years (31 yrs severe). 95% of posts on #MEcfs/#LongCovid/#chronicillness. 26 publications in peer-reviewed journals. @IrishMECFSAssoc trustee 28 yrs
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