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.

Our family supported Lili and her parents last year by either contributing in swimming miles or with fund raising events. This year we are supporting Lili same way as last year by contributing miles to cover 3600 kms and in process to raise much needed funds.