Emma Louise Foster Angel Fund

SMA UK is raising money for Spinal Muscular Atrophy (SMA) UK
In memory of Emma Louise Foster
SMA UK is a national charity supporting anyone affected by spinal muscular atrophy, a rare genetic, neuromuscular condition that causes muscle weakness and loss of movement. We offer support and information and advocate on issues important to the SMA Community.

Story

We lost our Daughter Emma in 1978 to type 1 Spinal Muscular Atrophy, or SMA.
SMA is a rare inherited neuromuscular condition. It may affect crawling and walking ability, arm, hand, head and neck movement, breathing and swallowing.
SMA UK is an established charity that supports and empowers anyone affected by the condition. They are advocates for better services, raise public awareness and fund research related initiatives. Thank you in advance for your generosity, it means a lot!


Donation summary

Total
£3,106.75
Online
£0.00
Offline
£3,106.75

Charities pay a small fee for our service. Learn more about fees