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Alexandra Hart raised £330 from 8 supporters
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Closed 01/04/2017
Weʼve raised £330 to help Sophia get the specialist equipment, physio and hydrotherapy she so desperately needs.
- Funded on Saturday, 1st April 2017
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Story
Sophia suffers from a rare genetic disability, spinal muscular atrophy (SMA) type 1. SMA is a terminal and degenerative disease that causes weakness and wasting of the voluntary muscles in infants and children. SMA impacts every muscle in the body hindering the ability to walk, sit, stand, eat, breathe and swallow. The mind always remains unaffected and children with SMA including Sophia are bright, sensitive and playful in spite of their failing bodies.
We are trying to raise money for Sophia's ongoing treatment in Paris, as the treatment is not available on the NHS, as well as ongoing costs of physio and hydrotherapy sessions.
Any donations big or small will be life changing for Sophia.
Thank you
Alexandra Madlin aka Auntie RaRa
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Supporters
8
The Gunay's
Mar 12, 2017
We saw Sophia's story on BBC News and fell in love with her!! Wishing her and her family all the best xxxx
£20.00
Anonymous
Mar 8, 2017
Anonymous
Mar 7, 2017
£50.00
Anonymous
Mar 2, 2017
Wishing Sophia and her family all the best.
Anonymous
Mar 2, 2017
£10.00
Frankie Ward
Mar 2, 2017
Good luck, I hope your family gets the help they need and deserve
£10.00
Anonymous
Mar 2, 2017
£10.00
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