Swim for Lili

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Team fundraiser • 4 members • The University of Edinburgh
£3,001
raised of £3,000 target
by 55 supporters
A SYNGAP1 gene mutation can cause a variety of symptoms that can range from mild to severe. The most common symptoms include learning difficulties, epilepsy, behavioural challenges, autism, and sensory processing disorder. Research is vital.

Story

A SYNGAP1 gene mutation can cause a variety of symptoms that can range from mild to severe. The most common symptoms include learning difficulties, epilepsy, behavioural challenges, autism, and sensory processing disorder. Research is vital.

Team members (4)

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About the campaign

A SYNGAP1 gene mutation can cause a variety of symptoms that can range from mild to severe. The most common symptoms include learning difficulties, epilepsy, behavioural challenges, autism, and sensory processing disorder. Research is vital.

About the charity

You can choose from a variety of Edinburgh projects to Fundraise Your Way for. All the money you raise is processed through the University of Edinburgh Development Trust (reg charity SC004307) ensuring 100% received goes directly to the cause you care about and put to use straight away. Thank You.
Find out more about fundraising with JustGiving

Donation summary

Total raised
£3,000.11
+ £324.20 Gift Aid
Online donations
£2,950.11
Offline donations
£0.00

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