INR 80 Lakhs Raised in 80 Minutes on Impact Guru by Delhi's Jangra Family for their Son's SMA Treatment

Being the only earning member in the family, Amit cannot afford his son's treatment, approximately INR 17.5 crores or USD 2.1 million. They are seeking support from generous donors via the route of medical crowdfunding. The family till date has crowdfunded INR 3.90+ crores with the generous support of 50,000+ donors across India.

Spinal Muscular Atrophy - Type 1 or SMA-1 is a genetic neuromuscular disorder that affects the nerve cells that control voluntary muscles (motor neurons). Without treatment, the progressive muscles develop weakness and eventually restrict any muscular movement including digestion, the beating of the heart muscle and lungs, and even the movement of the limb.

"Firstly, we are thankful to all the donors who have supported us till now. We were delighted the day Kanav was born and was handed in my arms by the doctors. We have always wished him to lead a normal and healthy life like other children, but fate had different plans for Kanav. Indeed, his life is not as easy as others, we will not lose hope. My baby does not deserve this pain and with your support, we can give him a second lease of life. He desperately needs the life modifying drug Zolgensma, a gene therapy for his SMA treatment. Your every tiny bit of donation will help my son take a positive step towards his treatment and a hope for a better future," appeals Kanav's father, Amit.

Note to editors: The treatment amount of INR 17.5 Cr. may vary as per the exchange rate of USD.