Our campaign is now complete. 145 supporters helped us raise £3,742.00
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The MPS Society is taking place in the Great North Run on 10th September 2023. Our runners are raising money for our members affected by MPS, Fabry and related lysosomal diseases.
The campaign has now expired but it's not too late to support this charity.
Visit the charity's profileOur 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!
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