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..