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We are raising money to fund a research project at Queens Square Neurology Institute, in the hope of curing SLC6A1 and changing lives

SLC6A1 is a debilitating condition caused by a mutation in the SLC6A1 gene. This effects brain function and causes a challenging epilepsy, learning disabilities, speech delay or absence, autism, ADHD, tremors, motor disorder and challenging behaviour. This is an ultra rare condition, and yet there are 6 children in Kent with the condition. Help us cure this disease.
This project successfully funded on 5th March 2024