Rachna Gupta

Bhavya and Aadvik Supporting Swim for Lili

Fundraising for The University of Edinburgh
£125
raised of £150 target
Donations cannot currently be made to this page
Swim for Lili, 31 March 2023
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

Bhavya and Aadvik are supporting by donating swim distance to a great cause and eager to raise awareness and funds as well! Please support.

This fund raising is being done by Aadvik’s class mate parents. I am super proud of my kids and while they donate the swim distance, I shall appreciate donations to encourage them. Please consider donating as little as you can. Every penny counts! 

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.

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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.

Donation summary

Total raised
£125.00
Online donations
£75.00
Offline donations
£50.00

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