Es gibt immer noch eine große Lücke zwischen dem, was die Öffentlichkeit über COVID-19 weiß, und dem, was sie wissen sollte. Deshalb hier Infos über COVID-19.

#CannabisMedizin🥦 #MEcfs🪫😷 #IchBinArmutsbetroffen💣 #GGUltra📎 ᓚᘏᗢᗢᘏᓗ ✨Anne Brorhilker Fan Club✨ I may be sick, but I won't be still.📢 Profilbild, schlafend

Living with Myalgic Encephalomyelitis, ME—not CFS.

Surviving MyalgicE aka ME/CFS & AAG to tell the story, pwME & advocate w/ a JD. Into MEdical, Social, Climate Justice & Arts. ME-dical apolide, Human Neutrino,

Finance & Art. History & Sociology & Fashion History. ME/CFS & LC 🫩

#artmoon #audhd.. Derping of the High Orders #teamblue #teamhumanity Music is life. Audhd. #Turing tests. Art. Life. Hypotheses. #alphabetchallenge 🔥🫵 #a

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

Author of "stranger and stranger”, letter writer, advocate and fundraiser for biomedical ME/CFS research.

Has the world gone insane? Brit in France. Ex-scientist. DPhil. Owned by cats. ME /CFS. Avatar: Proud Goose, Tui Sankamol

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