Doctors & Hospitals

12 Lakh+ Donors Contributed Over INR 125 Cr for Rare Disease Patients on ImpactGuru: Report, India’s leading integrated healthcare financing platform, reports one-of-its-kind, rare disease online donation crowdfunding movement with 12,00,000+ donors raising INR 125+ crore through 1200+ rare disease crowdfunding campaigns in 14 months (January 2021 to February 2022), for patients fighting rare diseases like Spinal Muscular Atrophy (SMA type 1 & 2), Gaucher’s disease, Pompe’s disease, rare forms of Cancer and others. 

The findings of ‘’s India’s Biggest Crowdfunding Movement For Rare Disease Report’ were revealed at the first edition of Impact Guru Excellence in Healthcare Summit and Awards 2022, on Rare Disease Day.

In a joint statement Co-Founders Piyush Jain and Khushboo Jain said, “Firstly, we applaud the government’s efforts to solve the issue of funding rare diseases and believe crowdfunding as one of the platforms for patients to receive funds whilst encouraging communities to donate for larger good under National Policy for Rare Diseases 2021. Donation crowdfunding has fundamentally changed people’s belief no matter how high the treatment cost, there is enough generosity for people to be able to find financing and receive access to quality healthcare. Having witnessed heightened generosity and multifold increase in rare disease fundraising in the past 14 months, our platform could help 4 SMA affected children (Teera Kamath, Ayaansh Gupta, Dhairyarajsinh, Ayansh Madan) get administered with the world’s most expensive gene therapy, while many other rare disease patients are in process to raise funds on ImpactGuru. We will continue to strive harder to work alongside concerned stakeholders to help patients and their affected families in providing them with the healthcare financing they need to recover.”

Alpana Sharma, Co-founder & Director-Patient Advocacy, CureSMA Foundation of India, said, “Alternative Healthcare Financing mechanism for rare diseases is the need of the hour. At present treatments for rare genetic diseases are not covered by insurance companies. Rare disease treatment is needed for life long and we lack an apt government scheme to support these patients and families. Presently, all the government schemes, both at the central and the state level are primarily for the BPL section leaving behind middle-income groups. A strong effort for effective provisions should be made for middle-class patients who are not covered under any government or private insurance. We strongly believe that platforms like are very well equipped to help bridge the gaps.” looks forward to helping more families in need to make sure that people get the right help at the right time to afford life-saving treatments for rare diseases.


Similar Posts

Leave a Reply

Your email address will not be published. Required fields are marked *