Weʼve raised £0 to Help children and adults live with Smith-Magenis Syndrome
- Closed on Wednesday, 24th October 2018
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Our little girl has a condition called smith-magenis syndrome. This effects her daily life both physically and mentally. Were quite lucky as our princess is quite low end spectrum. Some of these children can't sit, stand, talk or even eat unaided. I will anonymously be donating any funds raised to one family in need. (The family will be chosen by the ambassador of the smith magenis foundation).
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Chloe Eccles started crowdfunding
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