Thank you for helping to secure our work to support anyone affected by Spinal Muscular Atrophy, raise public awareness and fund research related initiatives. We couldn’t do it without you.

If you would like to read more about the Impact of our work in 2022 and our plans for 2023, please click here to read a letter from our previous CEO, Angela Smith-Morgan who was in post at this time. 

If you aren’t already familiar with SMA and our work, you may be interested to find out more: