Find support, or help research
People near you who know what living with ALS (motor neurone disease) is like, and ways you can help find better treatments.
Support groups in India
- ALS Care and Support Foundation India (ALSCAS)ALS Care and Support Foundation India: foundation in India supporting people with ALS/MND and their families with information and support.All of India
- Asha Ek Hope Foundation for MND/ALSAsha Ek Hope Foundation for MND/ALS: foundation in India supporting people with ALS/MND and their families with information and support.All of India
- Indian Organization for Rare DiseasesIndian Organization for Rare Diseases: national rare disease alliance in India supporting people with rare diseases; member of RDI.All of India
- Organization 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.All of India
Contact details come from each group's own page and are checked every 3 months.
Help research
You do not need to join a trial to help. Below are the programmes we found in India and how to reach them. You contact them yourself: Frontlight does not collect or pass on your details.
Give blood or tissue for researchResearchers use stored samples to find what causes ALS (motor neurone disease).
Share your health dataA registry collects health data, without your name, so research teams can study many people at once.
Take part as a healthy volunteerStudies need people without ALS (motor neurone disease) to compare with. Family and friends can help.