Walking for Smith-Magenis Syndrome
Toby was born with a rare chromosome disorder called Smith-Magenis Syndrome (SMS). He was diagnosed at the age of 18 months.
Raising money for
Smith-Magenis Syndrome Foundation UK
Donations accepted until 22-08-2017
We are raising money for the Smith-Magenis Foundation a charity that helps children of all ages and families living with condition. The foundation is a small charity that rely solely on fundraising and donations, so every penny counts.
On the 22nd July 2017 there is a group of us that are going to walk the Llangollen Round which is a 33ish mile high-level walk all in one day :)
Running / Walking
Event is completed
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with gift aid: £215.21
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