journalist, ORF, Vienna persistence > contacts + competence :)

Psychiatrist | Life on hold since Oct. '21 due to long Covid | LC foundation NL | Carpe diem sed non inpensa crastina | Tweets are my own | No medical advice

Dr. phil.; former professor; #Sozialpädagogik #Demokratiebildung #KinderundJugendarbeit #socialwork #Antifaschist #fcsp 🤎🤍❤️ Now #longcovid #mecfs emptystands.me Homepage: https://www.bildung.uni-siegen.de/mitarbeiter/fritz

Professor by Special Appointment - Head of Department of Ethics and Political Philosophy, Radboud Uni. Interests: Long Covid, Health Justice, Postviral Ethics, Trauma, Critical Theory,

Kinder- und Jugendlichenpsychotherapeut RPG-Fan, Oldtimer, Holzbau und Hühner

Austausch für Ärzt*innen, Mediziner*innen, Apotheker*innen und Psychotherapeut*innen, die von ME/CFS, LongCovid, PostVac und ähnlichen Erkrankungen betroffen sind.

Psychotherapie, Psychoanalyse, Psychotherapieforschung, ME/CFS

Physician | Scientist | working on Long Covid

Redakteur - APA Innenpolitik

psychologist | research associate @UniLeipzig | psychotherapist in training | my research is on psychologization & stigma of post-viral diseases

Psychiatrist, stigma researcher, w/ special interest in time trends and SUD stigma. Chair of Psychiatry at Leipzig University. Opinions are my own @MHandsociety.bsky.social

physician-researcher, paediatrician, ME/CFS since 2016. This account is about science, esp. CFS

An independent UK charity finding, funding, facilitating biomedical research into ME and providing better education and awareness of this disease in UK & Europe (charity nr. 1153730) www.investinme.org

The European ME Research Group (EMERG) is a collaborative network of researchers and clinician-researchers from across Europe, dedicated to advancing research into myalgic encephalomyelitis (ME, sometimes known as ME/CFS).

young European ME Research Group - A European forum formed with EMERG to support and encourage early career researchers in ME/CFS research https://youngemerg.com/index.shtml

Wir unterstützen Menschen mit ME/CFS (Myalgische Enzephalomyelitis / Chronisches Fatigue Syndrom) und setzen uns seit 1993 für Versorgung, Forschung und Aufklärung ein. Größte deutsche Patientenorganisation mit gut 3.000 Mitgliedern.

The European ME Alliance (EMEA) is a grouping of European organisations founded in 2008 by national patient organisations and charities across Europe, and dedicated to supporting patients suffering from Myalgic Encephalomyelitis (ME), also known as ME/CFS

Medizin-Redakteurin beim SPIEGEL, Biochemikerin, Buchautorin. https://www.spiegel.de/impressum/autor-de0618d4-0001-0003-0000-000000015007

Disease genomics & molecular mechanisms; ME/cfs: http://decodeme.org.uk, SequenceME @ Edinburgh University. Views - my own. He/him.

Empowering persons w Myalgic Encephalomyelitis. 35y w/ME Colab at ONG PEM Spain, ME-International.org, EMEA ICPrimer our best tool. #UniteToFight2024 Empoderando a #pcME. El Manual-CI nuestra mejor herramienta. Informando ME, MCAS, ANPE, LC