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£3,501.89
Lily's SMArt Fund Spinal Muscular Atrophy UK
Lily's SMArt Fund
£3,501.89
Spinal Muscular Atrophy UK
Lily's SMArt Fund
Lily's SMArt Fund

My SMArt Story

Our clever, cheeky, gentle little girl Lily was diagnosed with Spinal Muscular Atrophy type 2 at 16 months old. SMA is a rare, genetic, neuromuscular condition. In Lily's case, it means she won't walk. Her muscles in her neck, shoulders, core and hips are very weak. In the future, she might have breathing or swallowing problems as well. People with this condition tend to be very intelligent and Lily is no exception! Her speech is far more advanced than her years and she loves to sing in English, French and Italian. She is very generous and wants to share with and help everyone. She'd love it if you could support this cause. It is a small charity and every contribution, however small, makes a huge difference!

Thank You

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SMArt Funds

24 Aug 2017 24 Aug 2027 Visit this campaign

Donations Summary

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Charity

Spinal Muscular Atrophy UK