We did it!

Our campaign is now complete. 758 supporters helped us raise £22,633.00

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Closed 31/12/2023
The Society For Mucopolysaccharide Diseases (The MPS Society)

MPS Society TCS London Marathon 2023

The MPS Society has a great team of runners for the TCS London Marathon 2023 which takes place on Sunday 23rd April. Our runners are raising money for our members affected by MPS, Fabry and related lysosomal diseases.
£22,633
raised of £14,000 target
Donations cannot currently be made to this page
Event: London Marathon 2023, on 23 April 2023
Closed on 31/12/2023
RCN 1143472 and Scotland SC041012

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Story

We have an amazing team of runners who are training hard for the 2023 TCS London Marathon, which is taking place on 23rd April 2023. Our team is made up of Dave, Dale, Juan, David, Kevin, Stephen, Michael, Leanne and Caroline.

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.

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. Our team has already raised over £20,000 and they have well and truly smashed their original target!

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 MPS Society has been very helpful in sending supportive information and offering to put us in touch with other families who are affected by MPS. I know that in the difficult times to come, the MPS Society will be there for us.

To find out more about our amazing charity please head over to our website or email fundraising@mpssociety.org.uk.

Thank you.

About the charity

The Society For Mucopolysaccharide Diseases (The MPS Society)

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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 raised
£22,632.07
+ £3,854.86 Gift Aid
Online donations
£22,632.07
Offline donations
£0.00
Direct donations
£280.00
Donations via fundraisers
£22,352.07

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