50 Marathons for Lola

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Raising money for AT Society

The AT Society is the only charity supporting children and young people with Ataxia-Telangiectasia (AT) and funds for research to find a cure. We offer families an essential lifeline of advising and support through the many challenges they face. Life expectancy is currently just 26.

Story

Fast approaching 50, a drunken bet said we couldn't run 50 marathons before our birthdays next year. 50 by 50 is our pledge to run 50 x 26 miles between 23 Jul 21 and 23 Jul 22. Lacking any motivation (and obviously a few brain cells) I thought we should look for inspiration. The courage and determination shown by Lola and other children with Ataxia-Telangiectasia (“A-T”) every single day of their lives, puts our 12 month challenge into perspective. By the time we are 50, our struggle will be over, theirs won't. Please help us raise money and awareness for this very worthy cause!.

Ataxia-Telangiectasia (“A-T”) is a complex genetic disease which affects many parts of the body and causes severe disability. The symptoms include lack of balance, slurred speech and more than normal infections. The A-T Society is a small national charity unique to the UK in the services it offers families. The Society’s objective has been to alleviate the distress and suffering caused by A-T.The A-T Society provides support services for families, funds research and specialist A-T clinics, and helps raise awareness.

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Donation summary

Total
£3,313.15
+ £681.25 Gift Aid
Online
£3,313.15

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