We lost our daughter Martha to Spinal Muscular Atrophy (SMA) type 1 in September 2015 after only 6 months together.
The time after her diagnosis was confirmed in June was difficult but Martha also made it lots of fun and we had lots of adventures together. Martha made friends wherever she went with her engaging blue eyes and beaming smile. She flirted with the doctors and nurses caring for her, and had a cheeky, playful character.
We have decided to fundraise for the SMA Trust to aid research into SMA which will help families and children in the future.
