About KCNA2 Epilepsy

Global Alliance

KCNA2 Epileptic Encephalopathy

Why a Global Alliance

KCNA2 Epilepsy Global Alliance provides information and support for those who are diagnosed with KCNA2 and their families. Since the creation of our parent support group via Facebook in 2017, over 75 families from around the world have joined. Though there is currently no cure for KCNA2 Epilepsy, there is a need for advocacy, research opportunities, and effective treatment interventions.


The KCNA2 Epilepsy Global Alliance team includes the Board of Directors.  These parents and professionals volunteer their time, without compensation for their service.


The KCNA2 Epilepsy Global Alliance team includes The Scientific Advisory Board. Our scientific team is comprised of individuals dedicated to supporting families and advancing research, treatment options, and quality of life for individuals diagnosed with KCNA2.