MPS Society London Landmarks Half Marathon 2025

The MPS Society is taking part in the London Landmarks Half Marathon on 6th April 2025. Our runners are raising money to help support our members affected by MPS, Fabry and related lysosomal diseases.

London Landmarks Half Marathon 2025 · 6 April 2025 ·

Closes 31/12/2025

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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.

Story

6th April - the results!

What a team! Our runners absolutely smashed it running their hearts out on what was a stunning day with wall to wall sunshine! With Gift Aid, you have now raised over £5,000! The most ever raised for The MPS Society by a LLHM team! Well done and thank you so much for helping to make such a difference! #LLHM2025 #TeamMPS

4th April update!

We'd like to send a huge MPS THANK YOU to our runners for smashing their fundraising target. Well done Lianne, Helen C, Helen L, Alison, Claire, Sandra, Morgan and Frances, and also a special mention/thank you for Laura who was due to run but who has sadly had to pull out. You're a brilliant team and we can't wait to cheer you on!

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Our amazing team of runners are taking on the London Landmarks Half Marathon on 6th April 2025 and we can't wait to cheer them on!

Our team is aiming to raise over £3,000 so please spur them on with a donation. You can also come along on the day and cheer them on! As a small charity, we rely on events like this so we can continue to support our families.

The MPS Society provides vital support to families affected by one of 27 rare, life-limiting genetic conditions. We want all adults and children 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 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 or to register for one of our events, please take a look at our website or email fundraising@mpssociety.org.uk

Thank you to our team of runners and to all who support them. You are all wonderful! :)

Help The Society For Mucopolysaccharide Diseases (The MPS Society)

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Donation summary

Total
£4,192.00
+ £1,006.75 Gift Aid
Online
£4,192.00
Offline
£0.00
Direct
£395.00
Fundraisers
£3,797.00

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