We did it!

Our campaign is now complete. 145 supporters helped us raise £3,742.00

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Closed 01/06/2024
£3,742
raised of £2,000 target
Donations cannot currently be made to this page
Event: Great North Run 2023, on 10 September 2023
Closed on 01/06/2024
RCN 1143472 and Scotland SC041012

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Story

Our amazing team of runners are taking on the Great North Run on Sunday 10th September 2023.

Our team has already smashed their original target of £1,500 and more recently smashed their increased target of £2,000! Well done #TeamMPS. As a small charity, we rely on events like this so we can continue to support our families. Huge thank you to everyone who has donated so far!

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

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

To find out more about our amazing charity and how you can support us email fundraising@mpssociety.org.uk or take a look at our website.

Thank you to our team of runners and to all who support them. You're all wonderful!

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
£3,741.77
+ £765.88 Gift Aid
Online donations
£3,741.77
Offline donations
£0.00
Direct donations
£0.00
Donations via fundraisers
£3,741.77

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