MPS Society TCS London Marathon 2025

The MPS Society's 2025 team of runners will be raising money to help us support our members who are affected by MPS, Fabry and related lysosomal diseases by taking part in the TCS London Marathon on 27th April 2025.

£16,885
raised of £18,000 target

London Marathon 2025 · 27 April 2025 ·

Closes 31/12/2025

Be a fundraiser

Create your own fundraising page and help support this cause.

Start fundraising

Story

4th April update

Our team members are Tom, Ruth, James, Phil, Richard, Ashley, Josie, Cydney-Ann, Liz and Emily. They have recently smashed their original target of £15,000 and our runners are now aiming for £18,000. This will be such an incredible amount to raise for The MPS Society. Good luck #TeamMPS

Our MPS Society cheer squad will be between mile 14 and 15 on the day. Please pop by and say hi if you can! You won't be able to miss our blue flags, banners and pompoms!

_______________________________________________________

Our amazing team of runners are preparing to take on the ultimate challenge, the 2025 TCS London Marathon, which is taking place on 27th April 2025.

If you want to support our team, we'd love you to come along on the day and cheer them on. If you can't make it on the day, you can donate to an individual runner's page or spur on the whole team by donating via this page. You can also send good luck messages for them to the email address below.

The MPS Society provides vital support to families affected by one of 27 rare, life-limiting genetic conditions. We want all affected children and adults to have access to exceptional support and advice, world-class clinical care and effective treatments.

As a small charity, we rely on wonderful people like our team of runners to raise funds so we can transform the lives of those affected by these conditions.

The support from the MPS Society has been amazing: from always being there at the end of the phone to producing literature in non-medical language.

Events organised by the MPS Society have given us opportunities to connect with other families outside of the hospital environment, which has helped to build a network of support.

To find out more about our wonderful charity and the work we do, head to www.mpssociety.org.uk

To contact us, please email fundraising@mpssociety.org.uk

Thank you.

Help The Society For Mucopolysaccharide Diseases (The MPS Society)

Sharing this page with your friends could help raise up to 3x more in donations

You can also help by sharing this link on:

About the charity

The Society For Mucopolysaccharide Diseases (The MPS Society)

Verified by JustGiving

RCN 1143472 and Scotland SC041012
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.

Donation summary

Total
£16,884.61
+ £3,415.88 Gift Aid
Online
£16,384.61
Offline
£0.00
Direct
£0.00
Fundraisers
£16,884.61

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