Your friends are fundraising. Don't miss out, opt in.

Fundraiser complete

This page is now closed, but you can still donate to the cause directly

The Patton's Great Scottish Run page

David Patton is raising money for The Society For Mucopolysaccharide Diseases (The MPS Society)

Participants: Judith and Emma Patton

Donations cannot currently be made to this page

Great Scottish Run · 30 September 2018

The MPS Society provides specialist support to children, adults and families in the UK who are affected by MPS, Fabry and related lysosomal storage diseases and we fund research into treatment and therapies. These diseases are rare, genetic, life-limiting conditions with no cure.

Story

On 30 September my mum (Wee Jude), sister (Emma) and I will be taking part in the Great Scottish Run. It will be my mums first ever 10k and my first half marathon so hopefully we will be able to finish!! 

We will be raising funds for MPS Society, a charity that is very close to our hearts since my two sons, wife and wider family were diagnosed with fabry disease last year. Fabry is a rare genetic condition that leads to the failure of key organs in early life and similar to other rare diseases it often doesn't get the attention or funding that it needs.

MPS Society works tirelessly to support families with Fabry and other enzyme deficiency disorders through raising awareness, driving research in to new and improved treatments and providing invaluable ongoing support to families.

We will also be running in memory of my late father-in-law, Jim, who had Fabry but was never diagnosed and never had the opportunity to get treatment; highlighting the importance of raising awareness around these conditions and increasing the chances of early diagnosis.

Any contributions that you can give to this very worthy cause would be greatly appreciated

Donation summary

Total
£5,120.00
+ £753.00 Gift Aid
Online
£5,120.00
Offline
£0.00

Charities pay a small fee for our service. Learn more about fees