Toby is my 16yr old son who has Smith-Magenis-Syndrome. This run is

for him and all the other SMSERS out there.

The Smith-Magenis Syndrome (SMS) Foundation UK is at the heart of our community. We will be the first point of contact for those seeking information and support. Nobody should ever feel isolated or alone. We value every person affected by this genetic disorder and shall empower them to reach their full potential as respected members of society.

Connecting Families – Raising Awareness – Building Futures