Jason Smith

Jason's Cycling Across the Continent

Fundraising for The Society For Mucopolysaccharide Diseases (The MPS Society)
£3,235
raised of £2,500 target
by 82 supporters
Donations cannot currently be made to this page
The Society For Mucopolysaccharide Diseases (The MPS Society)

Verified by JustGiving

RCN 1143472 and Scotland SC041012
We support affected individuals & families to raise awareness of MPS diseases

Story

Thanks for taking the time to visit my JustGiving page.

I’m taking part in 2 long distance bike races, in 2018 I’m going to #BeMoreMike as in March 2017 we lost a cycling legend in Mike Hall. He inspired others to get out and ride. Mike’s death has had a fundamental affect on many lives but it has sent a message across the world to go out and do that bike ride.

Archie Pearson is my reason to fundraise for the MPS. He’s an active, football crazy, fun loving boy who has lived with MPS for over 10 years. Despite Archie’s battles with MPS he’s overcome such adversity to live his life by amazing us all in so many ways.

In 2018 Archie has been granted the “Make a Wish Campaign”. The MPS has provided vital life long weekly treatment for Archie and family support for over a decade. The MPS needs all the help it can to continue the life prolonging treatments that are so vital to the many MPS sufferers and families.

Every pound donated will make a huge difference to the MPS and give me even more reason to cycle faster, further and reach those finish lines in 2018. Thanks to each of the sponsors who have helped make these races possible and to support Archie and the MPS charity.

Donating through JustGiving is simple, fast and totally secure. Your details are safe with JustGiving - they'll never sell them on or send unwanted emails. Once you donate, they'll send your money directly to the charity. So it's the most efficient way to donate - saving time and cutting costs for the charity.

About the charity

The Society For Mucopolysaccharide Diseases (The MPS Society)

Verified by JustGiving

RCN 1143472 and Scotland SC041012
The MPS Society provides professional support to children, adults and families affected by MPS, Fabry and related Lysosomal Storage Diseases and funds research into treatment and therapies. These diseases are rare, genetic, life-limiting conditions.

Donation summary

Total raised
£3,235.00
+ £530.00 Gift Aid
Online donations
£2,910.00
Offline donations
£325.00

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