SYNGAP1 research at the Patrick Wild Centre

Arulmurugan Kalyanasundaram is raising money for The University of Edinburgh

Team: Hope for Syngap

£10
raised of £150 target by
1 supporter
Donations cannot currently be made to this page

500 miles

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.

I am fundraising with my friends to raise awareness of this rare condition.

Our team plans to do 3600KM by walk, run, swim, cycle by Oct 2024 and I hope to do 800KM of those..

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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
£10.00
+ £2.50 Gift Aid
Online
£10.00
Offline
£0.00

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