Whether you are a patient, a caregiver, a doctor or a supporter, we are here to help. The quickest way to reach us is on WhatsApp.
Choose whichever suits you best.
Office: 206, Duggal Complex, School Road, Khanpur, Delhi – 110062, India
Registered office: F-27, Institute of Medical Genetics & Genomics, Sir Ganga Ram Hospital, Rajinder Nagar, New Delhi – 110060, India
Please note: LSDSS is run by volunteers, so please allow some time for a reply. We can guide you, and in some cases help with the cost of supportive care such as surgery, but we cannot fund disease-specific treatment such as ERT or SRT, or give medical advice. In a medical emergency, go to your nearest hospital.
These pages may answer your question straight away.
Our volunteer state coordinators support families in their region, and spread awareness about LSDs among the public, doctors, the media and government officials.
Covers: Delhi NCR, Punjab, Haryana, Jammu and Kashmir, Ladakh, Himachal Pradesh, Uttar Pradesh, Uttarakhand, Chandigarh
Covers: West Bengal, Arunachal Pradesh, Assam, Manipur, Meghalaya, Mizoram, Nagaland, Sikkim, Tripura
Covers: Bihar, Jharkhand, Chhattisgarh, Odisha
Covers: Telangana, Andhra Pradesh
Covers: Kerala, Lakshadweep
Covers: Tamil Nadu, Puducherry, Andaman and Nicobar Islands
Volunteer with LSDSS, or donate to support families living with lysosomal storage disorders.