Nick's London to Southend Bike Ride page

Nick Popplewell is raising money for The Society For Mucopolysaccharide Diseases (The MPS Society)
In memory of Grace Popplewell
Donations cannot currently be made to this page
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

We are raising money for the  MPS society in memory of Grace Popplewell.

Grace, our daughter was born on 11th January 2007, diagnosed with the genetic disorder MPS7 'Sly syndrome'. We were told her outcome was very poor and that she would be still born or live anything from a few minutes to a few hours. We praise God that Grace was a big part of our family for 5 weeks, but then sadly died 17th February 2007.  For their support and in memory of Grace and the ongoing research into MPS disorders, we would like to raise a little bit of cash from Nick's little bike ride!!!!!

Thank you all for your support.

Help Nick Popplewell

Sharing this cause with your network could help raise up to 5x more in donations. Select a platform to make it happen:

You can also help by sharing this link on:

Donation summary

Total
£378.50
+ £70.63 Gift Aid
Online
£378.50
Offline
£0.00

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