Imagine a child being born without the ability to fight even the smallest infection. For baby Jaasritha Sai, this was her reality.
She was born with 严重联合免疫缺陷 (SCID) — a rare genetic disorder where the immune system doesn’t function. Even a simple cold could be life-threatening.
Diagnosed at just six months old, baby Jaasritha spent most of her early life in hospital isolation. She later underwent a life-saving bone marrow transplant, costing over RM200,000, made possible with the support of MYPOPI and generous donors.
Today, she remains under treatment but is slowly regaining her strength and her smile.
We extend our heartfelt thanks to The Star for publishing her story and helping to raise vital awareness about SCID. Their support plays a crucial role in educating the public and giving rare diseases the attention they deserve.
Special thanks to Prof. Dr. Intan Hakimah Ismail, one of the dedicated doctors who helped diagnose and treat baby Jaasritha, and continues to advocate for early detection of rare immunodeficiency conditions.
