SLC6A1 Connect

Global Genes Global Advocacy Alliance member focused on rare disease support, education, advocacy, or research. SLC6A1 Connect is a patient advocacy group dedicated to improving the lives of children and families affected by SLC6A1. SLC6A1 epileptic encephalopathy is a rare neurological condition in small children that causes seizures, severe movement and speech disorders and intellectual disability. Our group is led by and comprised of passionate and relentless parents of kids with SLC6A1. Our mission is to advance scientific research that will ultimately result in a disease modifying treatment. Directory information only; not medical advice, legal advice, or endorsement. Services and eligibility should be confirmed with the organization.