We're Here to Help You

Taraasha Foundation is an NGO dedicated to supporting families affected by Lysosomal Storage Disorders (LSDs) in India. We provide free helpline support, connect families with medical specialists, raise awareness, and advocate for better rare disease policies.

Anyone affected by an LSD — patients, families, caregivers, doctors, researchers, and well-wishers — is welcome to reach out. Our helpline and email are open to everyone seeking guidance, information, or support.

Yes, our helpline +91 98113 11920 is completely free. We do not charge any fee for counselling, referrals, or guidance. Our goal is to ensure no financial barrier stops a family from getting the help they need.

Absolutely. We maintain a directory of metabolic disease specialists and LSD-focused centres across India. Contact us on the helpline or by email and we will connect you with the most suitable specialist for your child's condition.

We cover the entire spectrum of Lysosomal Storage Disorders, including Gaucher disease, Fabry disease, MPS (Mucopolysaccharidoses), Pompe disease, Niemann-Pick disease, Fucosidosis, and many others.

We currently focus on navigation, counselling, and advocacy rather than direct financial disbursement. However, we can help families apply for government schemes, pharmaceutical compassionate-use programmes, and other funding sources.