Support organisations
Patient groups and helplines near you, for people with a disease and for their families.
72 organisations for Long COVID and ME/CFS in all countries
#MEAction Network
Find a doctor, find your group, crisis resources, handouts, MEpedia, Stop Rest Pace; branches in the US, UK and Scotland.
For Long COVID and ME/CFS
Visit site: meaction.netABEMDIS - Associação Brasileira de Encefalomielite Miálgica e Disautonomia
Patient-founded national association for people with myalgic encephalomyelitis and dysautonomia in Brazil, offering information, free WhatsApp support groups and advocacy.
For Long COVID and ME/CFS
Visit site: abemdis.org.br
Action for M.E.
Information and support team, free counselling and online community for young people, family support, guidance on school and university.
For Long COVID and ME/CFS
Visit site: actionforme.org.ukAliança Millions Missing Brasil (AMM Brasil)
Brazilian association offering awareness, advocacy and support for people with ME/CFS, Long COVID and other infection-associated chronic conditions.
For Long COVID and ME/CFS
Visit site: ammbrasil.com.brAltea Long COVID Network
Directory of long COVID clinics, doctors and therapists by canton, self-help guide, members' forum; in German, English, French, Italian.
For Long COVID and ME/CFS
Visit site: altea-network.comAmerican ME and CFS Society (AMMES)
US national nonprofit serving ME/CFS patients and caregivers through support, advocacy and education, with treatment info, support group listings and a crisis fund.
For Long COVID and ME/CFS
Visit site: ammes.org
ANZMES – Associated New Zealand Myalgic Encephalomyelitis Society
Associated New Zealand Myalgic Encephalomyelitis Society (ANZMES): patient organisation in New Zealand supporting people affected by ME/CFS and long COVID; member of the World ME Alliance.
For Long COVID and ME/CFS
Visit site: anzmes.org.nz
Asociacija „Savarankiškas gyvenimas“
Lithuanian association founded in 2017 for independent living of people with disabilities, the EMEA member for ME/CFS.
For Long COVID and ME/CFS
Visit site: savarankiskasgyvenimas.lt
Asociación de Personas con Encefalomielitis Miálgica (ONG-PEM)
Spanish association advocating for and supporting people with myalgic encephalomyelitis.
For Long COVID and ME/CFS
Visit site: ongpem.orgAssociation #ApresJ20 - Covid Long France
Patient association: guides for patients and families, peer support, rights (ALD, disability), work issues, symptom-tracking app, research participation. French member of Long Covid Europe.
For Long COVID and ME/CFS
Visit site: apresj20.fr
Bateman Horne Center
Non-profit ME/CFS and long COVID clinic (application and annual fee) plus free clinical care guide, crash survival guide, state resource directory, support groups.
For Long COVID and ME/CFS
Visit site: batemanhornecenter.org
C-support
Individual support for people with long-lasting COVID complaints. Closes at the end of 2026: finishing current cases; training for professionals continues.
For Long COVID and ME/CFS
Visit site: c-support.nuCFS/ME Associazione Italiana ODV
Volunteer ME/CFS association since 1991 (based at CRO Aviano): guides, FAQ, publications, awareness and research news. Email cfs@cro.it.
For Long COVID and ME/CFS
Visit site: stanchezzacronica.itCOVID-19 Longhauler Advocacy Project (C19LAP)
US patient-led nonprofit serving people with Long COVID and their families through advocacy, education, resources, chapters and support.
For Long COVID and ME/CFS
Visit site: longhauler-advocacy.org
Deutsche Gesellschaft fur ME/CFS e.V.
Hamburg-based ME/CFS association: plain-language information (PEM, pacing, orthostatic intolerance), FAQ incl. children and social-law questions, long COVID news, advocacy.
For Long COVID and ME/CFS
Visit site: mecfs.de
Društvo bolnikov ZEBRA
Slovenian non-profit for research, advocacy and support for people with ME/CFS and related chronic conditions.
For Long COVID and ME/CFS
Visit site: drustvobolnikovzebra.siEmerge Australia
Emerge Australia: patient organisation in Australia supporting people affected by ME/CFS and long COVID; member of the World ME Alliance.
For Long COVID and ME/CFS
Visit site: emerge.org.au
Fatigatio e.V. - Bundesverband ME/CFS
National ME/CFS patient association: 15 regional self-help groups, phone team, social-law help with applications, information booklets, annual conference (14 Nov 2026, Kassel and online).
For Long COVID and ME/CFS
Visit site: fatigatio.deFundacja ME/CFS Polska
Polish foundation for people with ME/CFS and Long COVID; awareness, education and advocacy.
For Long COVID and ME/CFS
Visit site: mecfs.pl
Invest in ME Research
UK charity run by patients and carers funding biomedical ME research and education.
For Long COVID and ME/CFS
Visit site: investinme.orgIrish M.E. Trust
Irish trust founded in 1989 providing information and counselling to people affected by ME.
For Long COVID and ME/CFS
Visit site: imet.ieKlub pacientů ME/CFS
Czech volunteer-run ME/CFS patients club.
For Long COVID and ME/CFS
Visit site: me-cfs.eu
Kontaktstelle für Selbsthilfegruppen (KoSe) – Amt für Soziale Dienste
Government contact point that sets up and supports self-help groups in Liechtenstein, incl. groups for depression, obesity, ME/CFS and Parkinson’s disease.
For Depression, Obesity, Long COVID and ME/CFS and 1 more
Visit site: llv.li
Long Covid Austria
Patient initiative: information for patients and relatives, list of contact points, closed Facebook peer group, myth-busting projects. Member of Long Covid Europe.
For Long COVID and ME/CFS
Visit site: longcovidaustria.at
Long Covid Belgium
Belgian French-speaking patient association for people with long COVID.
For Long COVID and ME/CFS
Visit site: longcovidbelgium.beLong COVID Campaign
Patient-led US nonprofit advocating for tests, treatments, research and programs for people living with Long COVID, with ways to get involved.
For Long COVID and ME/CFS
Visit site: longcovidcampaign.org
Long COVID Deutschland (initiative)
Patient-run initiative and directory: long COVID clinics, rehab, self-help groups, guides and research, advocacy. German member of Long Covid Europe.
For Long COVID and ME/CFS
Visit site: longcoviddeutschland.orgLong COVID Justice
Project by and for chronically ill and disabled people facing Long COVID, offering advocacy, a resource hub, webinars and support groups.
For Long COVID and ME/CFS
Visit site: longcovidjustice.orgLong Covid Kids
UK charity supporting children and young people with long COVID and their families.
For Long COVID and ME/CFS
Visit site: longcovidkids.orgLong Covid Nederland
Dutch long COVID patient initiative sharing knowledge and news and campaigning for patients.
For Long COVID and ME/CFS
Visit site: longcovidnederland.wordpress.com
Long Covid Support (Long Covid UK)
Charity set up by and for people with long COVID: information and support services, peer Facebook group (about 68,000 members), research involvement, campaigning.
For Long COVID and ME/CFS
Visit site: longcovid.orgLost Voices Stiftung
German foundation for people with ME/CFS offering awareness work, research funding, advocacy and a self-help network in Hannover.
For Long COVID and ME/CFS
Visit site: lost-voices-stiftung.orgMassachusetts ME/CFS & FM Association
Massachusetts non-profit serving people with ME/CFS, fibromyalgia and Long COVID, offering membership, peer support, a provider database, events and advocacy.
For Long COVID and ME/CFS
Visit site: massmecfs.org
ME Association
ME Connect freephone support line (Mon-Fri 10-17, Thu to 21, Sat 10-12) with signposting to local support groups; ME and long COVID information and research news.
For Long COVID and ME/CFS
Visit site: meassociation.org.uk
ME félag Íslands
Icelandic non-profit protecting the interests of people living with ME.
For Long COVID and ME/CFS
Visit site: mefelag.is
ME Foreningen
Danish independent non-profit ME patient association founded in 1992.
For Long COVID and ME/CFS
Visit site: me-foreningen.dkME/CFS Israel
ME/CFS Israel: patient organisation in Israel supporting people affected by ME/CFS and long COVID; member of the World ME Alliance.
For Long COVID and ME/CFS
Visit site: mecfsisrael.orgME/CFS-Selbsthilfe-Netzwerk Sachsen-Anhalt
Network of 13 self-help groups in 9 towns in Saxony-Anhalt for people with ME/CFS, Post-COVID, Post-Vac and PoTS and their relatives.
For Long COVID and ME/CFS
Visit site: mecfs-netzwerk-lsa.info
ME/cvs Vereniging
Patient organisation for ME/cvs: helpline (Mon 19-20, Wed 11-13, Fri 10-12.30), advice on care, education and benefits, magazine, advocacy.
For Long COVID and ME/CFS
Visit site: me-cvsvereniging.nlME|FM Society of BC
British Columbia non-profit formed to help and support patients with myalgic encephalomyelitis (ME/CFS) and fibromyalgia.
For Long COVID and ME/CFS
Visit site: mefm.bc.ca
MECVS Nederland
Dutch patient organisation for everyone with ME/CFS and their supporters, active for over 35 years.
For Long COVID and ME/CFS
Visit site: mecvs.nlMillions Missing France
ME/CFS association: listening and reliable information, referral to professionals and disability aid (MDPH, RQTH), pacing guidance, online and in-person support groups.
For Long COVID and ME/CFS
Visit site: millionsmissing.fr
Myos – Associação Nacional contra a Fibromialgia e Síndrome de Fadiga Crónica
Portuguese national patient association for fibromyalgia and chronic fatigue syndrome / myalgic encephalomyelitis, providing information and support.
For Long COVID and ME/CFS
Visit site: myos.ptNational ME/FM Action Network
Canadian registered non-profit dedicated to advancing recognition, education and support for people with myalgic encephalomyelitis (ME/CFS) and fibromyalgia.
For Long COVID and ME/CFS
Visit site: mefmaction.comNichtGenesenKids e.V.
Nationwide German non-profit supporting families, children, youth and adults with ME/CFS, Long COVID and Post-Vac via self-help meetings, information and advocacy.
For Long COVID and ME/CFS
Visit site: nichtgenesenkids.de
Norges ME-forening
Norwegian patient organisation representing over 5,000 ME patients since 1987.
For Long COVID and ME/CFS
Visit site: me-foreningen.no
Osterreichische Gesellschaft fur ME/CFS (OG ME/CFS)
Information on ME/CFS and post-COVID, guide for home care of severe ME/CFS, networking, support fund for patients, advocacy. Contact contact@mecfs.at.
For Long COVID and ME/CFS
Visit site: mecfs.at
PostCovid NL (Longfonds)
Patient organisation for long-lasting complaints after COVID: information, peer contact (one-to-one or groups), online forum, theme meetings, symptom tips.
For Long COVID and ME/CFS
Visit site: postcovidnl.nl
Riksförbundet för ME-patienter (RME)
Swedish independent membership organisation improving the situation of people with ME.
For Long COVID and ME/CFS
Visit site: rme.nuSahana South Asia
Regional initiative bringing together patients, caregivers, clinicians and researchers around post-viral fatigue, Long COVID and ME/CFS, with a Sri Lanka and South Asia focus.
For Long COVID and ME/CFS
Visit site: sahanasa.wordpress.com
Solve M.E.
Patient and caregiver resources, find-a-doctor guide, clinical trial list, unhide patient registry, research grants, advocacy for ME/CFS and long COVID.
For Long COVID and ME/CFS
Visit site: solvecfs.orgSteungroep ME en Arbeidsongeschiktheid
Dutch support group for people with ME/CFS facing work disability issues.
For Long COVID and ME/CFS
Visit site: steungroep.nl
Suomen lääketieteellinen ME/CFS-yhdistys
Finnish ME/CFS association working for better care and offering patients and families tools such as school support materials.
For Long COVID and ME/CFS
Visit site: slme.fi
Suomen ME/CFS-yhdistys (SMEY)
Finnish association founded in 2013 to help and support ME/CFS patients.
For Long COVID and ME/CFS
Visit site: smey.fi
Svenska Covidföreningen
Swedish patient association for people with long COVID.
For Long COVID and ME/CFS
Visit site: covidforeningen.seThe ME CFS Foundation South Africa
The ME CFS Foundation South Africa: foundation in South Africa supporting people affected by ME/CFS and long COVID; member of the World ME Alliance.
For Long COVID and ME/CFS
Visit site: mecfssa.org
Udruga za oboljele od ME, disautonomije i fibromialgije
Croatian association supporting patients with ME/CFS, dysautonomia and fibromyalgia and their families.
For Long COVID and ME/CFS
Visit site: mdf.hrUdruženje osoba sa sindromom hroničnog umora Srbije (SHUKS)
Serbian association of people with chronic fatigue syndrome (ME/CFS), a full member of the European ME Alliance; brings patients and professionals together and raises awareness.
For Long COVID and ME/CFS
Visit site: shuks-udruzenje.rs
Verein Long Covid Schweiz
Patient association: peer advice, multilingual Facebook group, information on symptoms and care, guides, insurance information, section for children, advocacy.
For Long COVID and ME/CFS
Visit site: long-covid-info.ch
Verein ME/CFS Schweiz
Information platform, peer support and networking, members' regional groups and coaching, events (e.g. social insurance, 11 Nov 2026), advocacy.
For Long COVID and ME/CFS
Visit site: mecfs.chМЕ/СХУ България
Bulgarian group raising awareness of ME/CFS and supporting people with the condition.
For Long COVID and ME/CFS
Visit site: opencollective.com
筋痛性脳脊髄炎の会
Japan ME Association (JMEA): patient organisation in Japan supporting people affected by ME/CFS and long COVID; member of the World ME Alliance.
For Long COVID and ME/CFS
Visit site: mecfsjapan.com
CONFESQ – Coalición Nacional de Fibromialgia, Síndrome de Fatiga Crónica, Electrohipersensibilidad y Sensibilidad Química Múltiple
Spanish national coalition of over 60 patient associations for fibromyalgia, ME/CFS and related conditions.
For Long COVID and ME/CFS
Visit site: confesq.org
Federació Andorrana d'Associacions de Persones amb Discapacitat (FAAD)
FAAD federates Andorran disability and patient associations, incl. AAMA (Alzheimer's), TRANAem (multiple sclerosis) and AMARE (rheumatic, ME/CFS).
For Alzheimer disease, Multiple sclerosis, Long COVID and ME/CFS and 1 more
Visit site: faad.ad
Long COVID Alliance
Network of patient advocates, scientists and experts (1,500+ members): patient resources, research library, clinical trials list, advocacy.
For Long COVID and ME/CFS
Visit site: longcovidalliance.orgEuropean Federation of Neurological Associations (EFNA)
Umbrella of 21 pan-European neurology patient groups; map of European neurology patient organisations.
For Alzheimer disease, Parkinson disease, Multiple sclerosis and 1 more
Visit site: efna.net
European ME Alliance (EMEA)
Grouping of national ME organisations in about 20 countries: ME guidelines, fact sheets, country member pages; leads patient involvement in the EU DISCOVER-ME project.
For Long COVID and ME/CFS
Visit site: euro-me.org
European ME Coalition
Patient- and carer-led European ME/CFS advocacy for biomedical research funding (EU Parliament petition and resolution).
For Long COVID and ME/CFS
Visit site: europeanmecoalition.com
Long COVID Europe
Patient-run European network of Long COVID associations: shares information and contacts, pushes for recognition, patient-focused research and rehabilitation; WHO/Europe collaborating partner.
For Long COVID and ME/CFS
Visit site: longcovideurope.orgWorld ME Alliance
Global alliance of national ME/CFS organisations (formerly IAfME): coordinated policy dialogue, shared advocacy resources; also covers post-COVID conditions.
For Long COVID and ME/CFS
Visit site: worldmealliance.orgEuropean Patients' Forum (EPF)
Umbrella of European patient organisations and national patient coalitions.
For any disease
Visit site: eu-patient.eu
International Alliance of Patients' Organizations
Global alliance of patient organisations of all diseases, promoting patient-centred healthcare.
For any disease
Visit site: iapo.org.uk
Do you know an organisation we missed? Write to support@frontlightresearch.com and we will add it.