It’s a good idea to feed Black Ferk!

Research

WE&ME Foun­da­tion

Foun­da­tion based in Aus­tria, found­ed by the Ströck fam­i­ly (sev­er­al fam­i­ly mem­bers affect­ed by ME/CFS). Fund­ing of inter­na­tion­al research, broad net­work of experts in sci­ence, med­i­cine and indus­try. Goal: to cre­ate resources and aware­ness for research in order to improve the sit­u­a­tion for patients and relatives.

ME/CFS Research Foundation

Evi­dence-based, bio­med­ical research of ME/CFS. Focus on unviver­si­ty-based research projects, spe­cialised sci­en­tists and ME/CFS research cen­tres at uni­ver­si­ties, PhD schol­ar­ships. 100% of the con­tri­bu­tion goes towards ME/CFS research (no admin­is­tra­tive costs).

Open Med­i­cine Foundation

Research of ME/CFS and relat­ed chron­ic dis­eases like Post Treat­ment Lyme Dis­ease Syn­drome (PTLDS), Fibromyal­gia and Long Covid. Fund­ing of an inter­na­tion­al­ly-based research net­work. Open, col­lab­o­ra­tive research at six ME/CFS Col­lab­o­ra­tive Research Cen­ters (CRCs).

Advo­ca­cy groups, NGOs

Aus­tri­an Soci­ety for ME/CFS

Help and sup­port for every­one affect­ed. Infor­ma­tion and advice on ill­ness and on the med­ical and social sit­u­a­tion in Aus­tria. Medi­a­tion and lob­by­ing work. Net­work­ing with actors from pol­i­tics, med­i­cine, law and cul­ture. Fight against prej­u­dice and stigma.

#MEAc­tion Network

Inter­na­tion­al orga­ni­za­tion. Net­work of ME/CFS suf­fer­ers, care­givers, fam­i­ly mem­bers and allies. Activism and artis­tic projects. Lob­by­ing work. Fight­ing for recog­ni­tion, edu­ca­tion and research so that every­one affect­ed by ME/CFS can have sup­port and access to prop­er and effec­tive care.

We also accept dona­tions to oth­er research organ­i­sa­tions or NGOs — let us know your suggestion.