Bhavya and Aadvik Supporting Swim for Lili

Rachna Gupta is raising money for The University of Edinburgh

Team: Swim for Lili

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.

Help Rachna Gupta

Sharing this cause with your network could help raise up to 5x more in donations. Select a platform to make it happen:

You can also help by sharing this link on:

Donation summary

Total
£125.00
Online
£75.00
Offline
£50.00

Charities pay a small fee for our service. Learn more about fees