How we help
From the day of diagnosis onwards, we offer practical, emotional and financial support to people with SMA and their families — free of charge.
Family counselling
We help parents come to terms with the diagnosis, explain what to expect, and connect them with families facing similar challenges.
Who it's for: Newly diagnosed families and anyone who needs to talk.
Genetic counselling
Understand test results, the cause and pattern of inheritance, treatment options, and carrier testing for the wider family.
Who it's for: Parents, siblings and relatives; couples planning a pregnancy.
SMA clinics
Multidisciplinary clinics where neurologists, orthopaedic and spine surgeons, pulmonologists, dieticians and physiotherapists see patients together.
Who it's for: Children and adults with SMA.
Financial aid
Support for families who cannot afford assistive devices, surgery or hospital care.
Who it's for: Registered members who meet the eligibility criteria.
Awareness & education
Booklets and leaflets, webinars on care, regional parent meetings and our national conference, SMArtCon.
Who it's for: Families, doctors and the public.
Advocacy
Working with ministries, regulators, insurers and industry for faster approvals, affordable treatment and inclusion in government schemes.
Who it's for: The whole SMA community.
Getting support starts with registering
Registering with Cure SMA India is free. It lets us reach out to you, include you in clinics and programmes, and represent the needs of every Indian SMA family to policy-makers.
Register with usWe receive no government funding
Our programmes are funded by members and supporters. A donation helps us reach more families.
Help a family facing SMA today
We receive no government funding. Your gift pays for counselling, clinics, assistive devices and hospital care for families who cannot afford them. Donations are eligible for tax benefit under Section 80G.