Evidence-based medicine over eminence-based medicine. #MECFS
Facharzt für Innere Medizin | Nephrologe | Geriater | interessiert an #PAIS und assoziierten Multisystemerkrankungen |
* Privat gerne alles mit Musik *
* Skeets in DE/EN *
* TwiX: @CBammerMD *
Immunologist and ME/CFS researcher @Charité
https://cfc.charite.de/
#MECFS #MILLIONSMISSING #MEAwareness
#PEM #POTS #MCAS
#PostCovid #LongCovid
#TeamWissenschaft #GdB
https://www.mecfs.de/was-ist-me-cfs/
Facharzt für Neurologie
ME/CFS ▪ Long Covid ▪ Nervenultraschall ▪ ENG/EMG ▪ Hirngesundheit ▪ Telemedizin
Long Covid enthusiast 🙃. Physicist. Father. 🇦🇹
ME/CFS seit 2019. Ich setze mich für bessere Aufklärung, Versorgung und Forschung ein, die aufgrund jahrzehntelanger falscher Einordnung als psychische Krankheit bisher kaum stattgefunden hat.
27 / Life on pause since 12/21 due to #LongCovid #MECFS Type
#ITSlive #Impfluencer #ABS #MECFS
Anästhesist und Intensivmediziner 🚑
Aus Leipzig 🖤❤️
#linksversifft
#FCKAFD #NieWiederlstJetzt
#KlimaschutzMussJetzt
Ich bin auch dort 👉🏻 https://mastodon.de/@Intensivdiva
Chronically ill mess, JRA, IgA vasculitis, long covid, CFS
Librarian, artist, gamer and streamer ✨️
Früher mal Tech-Journalist. Heute berufsunfähig dank Covid-Infektion.
chronic illness life & disability lit 📚🪴🌊🐕
honoring the hard & finding joy along the way
migraine | SF neuropathy | POTS | ME/CFS |
long COVID | MCAS | ambulatory ♿
Chronic Illnese and Disability education and advocacy. 🐙
Severe MECFS warrior with Long Covid, Dysautonomia (POTs and low blood volume), Fibromyalgia, Endometriosis, Depression.🐙
Medical researcher + Medschool Dropout 🐙
Living with post-Covid ME/CFS, dysautonomia and Functional Neurological Disorder since a 2nd Covid reinfection in May 2022
Poet. Writing on disability & eco justice. Bedbound with Long COVID and Severe ME. 🍉 🇵🇸 🌲 🐦 😷
WILDNESS UNAFRAID, Kelsay Books (2026).
Pharmacist interested in Long COVID and ME/CFS research
Pro-mask, pro-clean air!
Substack: https://pharmd.substack.com/
We provide support, resources & reliable science-based information to patients, parents or caregivers of those suffering from Long Covid in Canada in our FB support group. Engaging w our community& building collaborations. Because we are STRONGER TOGETHER.
ME/CFS patient advocating for research, medical education, treatment and support re: Myalgic Encephalomyelitis/Chronic Fatigue Syndrome