www.covidactionscotland.org #COVIDAwareness #LongCOVID #COVID #PublicHealth

We're an independent, patient-led, international discussion forum (www.s4me.info) for people with ME/CFS and carers, clinicians, scientists and advocates who su

I occasionally try to explain and comment on ME research, or even contribute to it. And I advocate for more and better research.

Independent historical researcher (involuntarily self-taught), writing at a frustratingly slow 🐌 pace due to severe chronic illness.

ME - patient/advocate LC, ME/CFS & more; RACE - human; RELIGION - truth; BIAS - unbiased integrity/evidence based science/reality; AVERSIONS - money, ego & powe

Interested in research into ME/CFS/MECFS, FND and related conditions. https://medium.com/@cfs_research

ME. Spouse w LC, ME. Writer, bread baker, daydreamer. Still waiting on fair funding and apology from HHS. Masking like someone’s life depends on it.

Body malfunctioning since 1998 #MECFS #PoTS #MCAS #hypermobility & other delights. I'm a #LongCovid #LongCovidKids and #Pans #Pandas ally. Here to make connect

Evidence-based medicine over eminence-based medicine. #MECFS

Living with ME/CFS since 1983. An advocate since my diagnosis in 1988.

Bin wirklich kein Doktor und auch kein Agentur-Account #TeamWissenschaft! Aktuelles zu #FakeNius. Querdeppen, #PostVac und sonstigen Schwurbel Ehemals https://x

95% of posts on #MyalgicEncephalomyelitis, #LongCovid or #chronicillness. With ME/CFS 37 years, severe ME 32 years. @IrishMECFSAssoc trustee 29 years 26 publ

Irish Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Association-for Information, Support & Research NB: Posts ≠ advice. Registered Charity RCN 20100254.