27 September 2022 — 18 May 2024
Nafisa Foundation
She was born an angel and she died an angel. Her memory now carries other children to care.
Our promise
- $0
- given directly to families
- 0
- payments made, each with a QR receipt
- 72 hours
- emergency turnaround — one to two weeks otherwise
Nafisa's story
Nafisa was born on 27 September 2022 and lived with SMA Type 1. A community across the world came together and raised one million US dollars for her gene therapy. On 18 May 2024, at nineteen months old, she passed away. The love that gathered around her did not end there. Nafisa Foundation exists to give that love back as medical aid: children first, adults in time.
In her memory
1. You apply
Tell us about the patient, the diagnosis, the hospital and the cost. Upload the medical letters and reports — everything stays private and encrypted.
2. A doctor reviews
A medical reviewer reads the case and recommends. Then we decide the amount of help we can honestly give.
3. We pay, and we prove it
You send your bank or mobile money details on a one-time secure link. When we pay, you get a receipt with a QR code anyone can verify.
Our partners
Yusufali Trust
A founding partner supporting medical aid cases alongside Nafisa Foundation.
Given with love, together
Nafisa Foundation
In her name, for other children
Yusufali Trust
Partner in giving