Support organisations
Patient groups and helplines near you, for people with a disease and for their families.
52 organisations for Neuromyelitis optica (NMOSD) in all countries

Advocacy Service for Rare and Intractable Diseases (ASrid)
Advocacy Service for Rare and Intractable Diseases (ASRID): patient organisation in Japan supporting people with rare diseases; member of RDI.
For Amyloidosis, Neuromyelitis optica (NMOSD)
Visit site: asrid.org
Asociación de Lucha Contra la Esclerosis Múltiple (ALCEM)
Association for the Fight against Multiple Sclerosis (ALCEM): patient organisation in Argentina supporting people with multiple sclerosis and neuromyelitis optica (NMOSD) and their families.
For Multiple sclerosis, Neuromyelitis optica (NMOSD)
Visit site: alcem.org.arAsociación Española NMOSD: NMO y MOGAD
Spanish association for people with neuromyelitis optica and MOG antibody disease and their families, providing support, treatment and information.
For Neuromyelitis optica (NMOSD)
Visit site: esnmosd.orgAssociazione Italiana NMOSD e MOGAD (AINMO)
Italian patient association for people with NMOSD and MOGAD and their families: information, support and advocacy.
For Neuromyelitis optica (NMOSD)
Visit site: ainmo.it
Casa Hunter
Casa Hunter: patient organisation in Brazil supporting people with rare diseases; member of RDI.
For ALS (motor neurone disease), Amyloidosis, Cystic fibrosis and 16 more
Visit site: casahunter.org.br
Esclerosis Múltiple Argentina (EMA)
Multiple Sclerosis Argentina (EMA): patient organisation in Argentina supporting people with multiple sclerosis and neuromyelitis optica (NMOSD) and their families.
For Multiple sclerosis, Neuromyelitis optica (NMOSD)
Visit site: ema.org.arFundación Colombiana para Enfermedades Huérfanas (FUNCOLEHF)
Fundación Colombiana para Enfermedades Huérfanas (FUNCOLEHF): foundation in Colombia supporting people with rare diseases; member of RDI.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: enfermedadeshuerfanas.org.co
Genetic and Rare Diseases Information Center
NIH information center (GARD) providing reliable information on genetic and rare diseases to patients and families via website and contact center.
For Glioblastoma, Acute myeloid leukemia, Hodgkin lymphoma and 32 more
Visit site: rarediseases.info.nih.gov
Instituto Vidas Raras
Rare Lives Institute: patient organisation in Brazil supporting people with rare diseases; member of RDI, IPA.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: vidasraras.org.br
Malaysian Rare Disorders Society (MRDS)
Malaysian Rare Disorders Society (MRDS): patient organisation in Malaysia supporting people with rare diseases; member of RDI.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: mrds.org.myMS Vereniging Nederland
MS-telefoon (workdays 10.30-14, WhatsApp any time) with volunteers, 19 regions with contact groups, partner and youth groups, webinars, nutrition line for members.
For Multiple sclerosis, Neuromyelitis optica (NMOSD)
Visit site: msvereniging.nlMS-Liga Vlaanderen vzw
Flemish MS patient association with 20+ local branches, a social service and volunteers; its site has a dedicated NMOSD and MOGAD section.
For Neuromyelitis optica (NMOSD)
Visit site: ms-vlaanderen.be
MSキャビン(MS Cabin)
MS Cabin: patient organisation in Japan supporting people with multiple sclerosis and neuromyelitis optica (NMOSD) and their families.
For Multiple sclerosis, Neuromyelitis optica (NMOSD)
Visit site: mscabin.orgNMO France
French patient association for people with neuromyelitis optica, NMOSD and MOGAD, offering information, peer exchange and guidance for patients and carers.
For Neuromyelitis optica (NMOSD)
Visit site: nmo-france.org
Rare Diseases Ghana Initiative
Rare Diseases Ghana Initiative: patient organisation in Ghana supporting people with rare diseases; member of RDI.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: rarediseaseghana.org
Rare Diseases Society Nepal
Rare Diseases Society Nepal: patient organisation in Nepal supporting people with rare diseases; member of RDI.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: rarediseasenepal.org
Rare Disorders Kenya
Rare Disorders Kenya: patient organisation in Kenya supporting people with rare diseases; member of RDI.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: rarediseasekenya.org
Rare Disorders Zimbabwe (RDZ)
Rare Disorders Zimbabwe (RDZ): patient organisation in Zimbabwe supporting people with rare diseases; member of RDI.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: raredisorderszim.org
Shoqata e Sëmundjeve të Rralla
The Rare Diseases Association Albania is an NGO organising patients and active people in the rare disease field to improve their quality of life.
For Glioblastoma, Acute myeloid leukemia, Childhood cancers and 34 more
Visit site: rda-al.com
Thai Rare Disease Foundation
Thai Rare Disease Foundation: foundation in Thailand supporting people with rare diseases; member of RDI.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: thairdf.orgUAE Rare Disease Society
UAE Rare Disease Society: patient organisation in United Arab Emirates supporting people with rare diseases.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: uaerds.ae
بنیاد بیماری های نادر ایران
Rare Disease Foundation of Iran (RADOIR): foundation in Iran supporting people with rare diseases; member of RDI, FIN.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: raredisease.ir
病痛挑战基金会
Illness Challenge Foundation: foundation in China supporting people with rare diseases; member of RDI.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: chinaicf.org財團法人罕見疾病基金會
Taiwan Foundation for Rare Disorders: foundation in Taiwan supporting people with Fabry disease, Pompe disease; member of IPA, FIN.
For Fabry disease, Pompe disease, Glioblastoma and 34 more
Visit site: tfrd.org.tw香港視神經脊髓炎協會 (NMOHK)
Registered non-profit patient organisation in Hong Kong for people with NMO and their carers, offering medical information, talks and peer support.
For Neuromyelitis optica (NMOSD)
Visit site: nmohk.com(사)한국희귀·난치성질환연합회
National federation of rare and intractable disease patient groups in Korea; runs policy advocacy, medical and welfare support and a shelter for rare disease patients and families.
For Glioblastoma, Acute myeloid leukemia, Childhood cancers and 34 more
Visit site: kord.or.kr
Alianza Argentina de Pacientes (ALAPA)
Alianza Argentina de Pacientes (ALAPA): national rare disease alliance in Argentina supporting people with rare diseases; member of RDI.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: alianzapacientes.org
Alianza Dominicana de Asociaciones de Pacientes (ADAPA)
Alianza Dominicana de Asociaciones de Pacientes (ADAPA): national rare disease alliance in Dominican Republic supporting people with rare diseases; member of RDI.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: adapa.org.do
Alianza Nacional por la Salud (ANS)
Quito-based alliance defending the right to health in Ecuador for patients with catastrophic, rare and orphan diseases; patient groups and foundations can join as members.
For Glioblastoma, Acute myeloid leukemia, Childhood cancers and 34 more
Visit site: ans.ecAssociação Brasileira de Enfermidades Raras (FEBER)
Associação Brasileira de Enfermidades Raras (FEBER): national rare disease alliance in Brazil supporting people with rare diseases; member of RDI.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: feberraras.wixsite.com
Canadian Organization for Rare Disorders
National umbrella network for organizations and people with rare disorders, providing a common voice to advocate for health policy and services.
For Glioblastoma, Acute myeloid leukemia, Childhood cancers and 34 more
Visit site: raredisorders.ca
Federación Argentina de Enfermedades Poco Frecuentes (FADEPOF)
Federación Argentina de Enfermedades Poco Frecuentes (FADEPOF): national rare disease alliance in Argentina supporting people with rare diseases; member of RDI.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: fadepof.org.ar
Federación Colombiana de Enfermedades Raras (FECOER)
Federación Colombiana de Enfermedades Raras (FECOER): national rare disease alliance in Colombia supporting people with rare diseases; member of RDI.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: fecoer.orgFederación Mexicana de Enfermedades Raras (FEMEXER)
Federación Mexicana de Enfermedades Raras (FEMEXER): national rare disease alliance in Mexico supporting people with rare diseases; member of RDI, FIN.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: femexer.org
Federación Peruana de Enfermedades Raras (FEPER)
Federación Peruana de Enfermedades Raras (FEPER): national rare disease alliance in Peru supporting people with rare diseases; member of RDI.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: feperperu.org
Indian Organization for Rare Diseases
Indian Organization for Rare Diseases: national rare disease alliance in India supporting people with rare diseases; member of RDI.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: rarediseases.in
MS Australia
MS Australia: national umbrella organisation in Australia supporting people with multiple sclerosis and neuromyelitis optica (NMOSD) and their families.
For Multiple sclerosis, Neuromyelitis optica (NMOSD)
Visit site: msaustralia.org.au
Nadir Hastalıklar Federasyonu
Turkish federation founded by rare-disease patients and families to raise awareness and address their problems; members are rare-disease patient associations.
For Glioblastoma, Acute myeloid leukemia, Childhood cancers and 34 more
Visit site: nadir.org.trNamibia Alliance for Rare Diseases
Namibia Alliance for Rare Diseases: national rare disease alliance in Namibia supporting people with rare diseases; member of RDI.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: rarediseasesnamibia.org
National Organization for Rare Disorders
US national rare disease alliance of patient organizations: education, patient assistance programs, rare disease database and policy advocacy.
For Glioblastoma, Acute myeloid leukemia, Childhood cancers and 34 more
Visit site: rarediseases.orgOrganization for Rare Diseases India (ORDI)
Organization for Rare Diseases India (ORDI): national rare disease alliance in India supporting people with rare diseases; member of RDI, IPA.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: ordindia.in
Philippine Society for Orphan Disorders (PSOD)
Philippine Society for Orphan Disorders (PSOD): national rare disease alliance in Philippines supporting people with rare diseases; member of RDI, IPA, FIN.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: psod.org.phRare Diseases South Africa
Rare Diseases South Africa: national rare disease alliance in South Africa supporting people with rare diseases; member of RDI, IPA, FIN.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: rarediseases.co.za
Rare Disorders NZ
Rare Disorders NZ: national rare disease alliance in New Zealand supporting people with rare diseases; member of RDI.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: raredisorders.org.nz
Rare Voices Australia
Rare Voices Australia: national rare disease alliance in Australia supporting people with rare diseases; member of RDI.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: rarevoices.org.au
Združenje za redke bolezni Slovenije (ZRBS)
ZRBS is a voluntary association of Slovenian patient societies for specific groups of rare diseases; it co-organises the national Rare Disease Day conference.
For Glioblastoma, Acute myeloid leukemia, Childhood cancers and 34 more
Visit site: zrbs.eu蔻德罕见病中心
Chinese Organization for Rare Disorders (CORD): national rare disease alliance in China supporting people with rare diseases; member of RDI.
For Acute lymphoblastic leukaemia, Acute myeloid leukemia, ALS (motor neurone disease) and 34 more
Visit site: cord.org.cn
EURORDIS – Rare Diseases Europe
Alliance of over 1,000 rare disease patient organisations, with a list of rare disease helplines by country.
For Glioblastoma, Acute myeloid leukemia, Childhood cancers and 35 more
Visit site: eurordis.orgThe Guthy-Jackson Charitable Foundation
NMOSD foundation (US-based, international reach): newly-diagnosed guides, patient resource guide, NMO Patient Days, directory of advocacy groups, expert-clinician map, research.
For Neuromyelitis optica (NMOSD)
Visit site: guthyjacksonfoundation.org
The Sumaira Foundation for NMO
NMOSD and MOGAD patient foundation (US-based): support groups, caregiver conversations, patient days, education brochures, webinars, assistance programmes.
For Neuromyelitis optica (NMOSD)
Visit site: sumairafoundation.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.