Tim Dawson

Collection for Louis Angelinetta's Leaving Do for SYNGAP1 research at the Patrick Wild Centre in memory of James Nash

Fundraising for The University of Edinburgh
£460
raised of £100 target
by 21 supporters
Donations cannot currently be made to this page
Leaving Do for Louis, 16 June 2022
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

With the passing of our good friend and colleague James Nash, Louis has asked that any collections towards his leaving do be donated to a charity close to James and Jo's heart - SynGap1 research

After 15yrs in the same building, having worked for 3 different companies in multiple roles and working his way up the corporate ladder Louis has decided to move on to different pastures. Louis will be sorely missed and we wish him all the best with his new adventure.

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 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.
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Donation summary

Total raised
£460.00
+ £77.50 Gift Aid
Online donations
£460.00
Offline donations
£0.00

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