I hope this post gets as many eyes on this as possible - please take a few minutes to read if you can.
Devdan is born with Type 2 Spinal Muscular Atrophy (SMA) – a rare condition that damages nerve cells in the brain and spinal cord. This leads to progressive muscular weakness and trouble with activities such as breathing, speaking, swallowing, and walking.
Zolgensma, is a ONE-TIME-ONLY gene therapy treatment for children aged under 2 years with SMA which costs $2.8 MILLION.
Devdan turns 2 in Oct so this is a race against time to raise this money before FDA will send this drug out. I myself have donated, and so far we have clocked over $1 million which is fantastic but we still have yet to reach our goal. Appreciate it if you can spare a donation - no amount is too small. 🙏🏼
Stay strong Devdan, always remember God is fighting with and for you. ❤️
DONATE HERE: https://rayofhope.sg/campaign/please-give-devdan-a-second-chance-of-life/
