"I want to hold on to hope." Baby Faziq has severe Spinal Muscular Atrophy (SMA), a rare genetic condition affecting muscle strength and movement. The gene therapy he requires costs S$2.4M — out of any family's reach.
Community is showing up via crowdfunding: at 5% of target, 823 donors and counting have contributed. Every donation, from $2 to $5,000, encapsulates well wishes and hope.
Our role is not to replace systems, but to respond thoughtfully in the space before solutions are formalised — so families are not left unsupported simply because structures have yet to catch up.
