Your Support Matters!
Our mission is to accelerate research to find a cure for KCNT1-related epilepsy.
You Can Make A Difference - Donate by Dec 31st
You Can Make A Difference - Donate by Dec 31st
Sending Birthday Wishes for those with KCNT1 Disorders
Sending Birthday Wishes for those with KCNT1 Disorders
Make a birthday donation to the KCNT1 Epilepsy Foundation
Be Counted! KCNT1 Inaugural Census Count!
Be Counted! KCNT1 Inaugural Census Count!
Citizen.Health
Citizen.Health
Transform hours of medical paperwork into instant answers with Citizen Health's AI Advocate. Built by rare disease families, for rare disease families, get answers to your questions about medications, treatments, and care coordination for rare diseases. Trusted by 50+ patient advocacy groups.
'This is real': Newport Beach family seeks to ensure rare disease funding continues
'This is real': Newport Beach family seeks to ensure rare disease funding continues
Bilingual Volunteers Needed for KCNT1
Bilingual Volunteers Needed for KCNT1
SAMi | The Nighttime Sleep Activity Movement Monitor
SAMi | The Nighttime Sleep Activity Movement Monitor
Experience peace of mind with SAMi, the no-wearable sleep monitor providing real-time alerts & recordings for those with movement disorders
Sign-up!
Subscribe to our Newsletter
Subscribe to our Newsletter
Stay informed with the latest news, research updates, and community events from the KCNT1 Epilepsy Foundation.
Doctor Registration Home — KCNT1 Epilepsy Foundation
Doctor Registration Home — KCNT1 Epilepsy Foundation
Are you a medical professional treating KCNT1 epilepsy? Register with our foundation to support patient care and research.
Join our Professional Network - For researchers and clinicians
Join our Professional Network - For researchers and clinicians
Connect and collaborate with other scientists, clinicians, and stakeholders to further our understanding of KCNT1 related disorders and accelerate the development of treatments and cures. Subscribe to receive updates, special announcements, grant notifications, and invitations to attend Research Roundtables and other opportunities to meet, share, and learn. If you are a clinician, we also invite you to add your contact info to our special directory: https://kcnt1epilepsy.org/doctor-registration
KCNT1 Birthday Announcement Sign-up Form
KCNT1 Birthday Announcement Sign-up Form
Access Google Forms with a personal Google account or Google Workspace account (for business use).
In the News
Meet Alexandria Wild, @Georgia Power 's Environmental Affairs team and mother to Emmy
Meet Alexandria Wild, @Georgia Power 's Environmental Affairs team and mother to Emmy
Meet Alexandria Wild, permitting engineer for Georgia Power 's Environmental Affairs team and mother to Emmy. Emmy was diagnosed with a mutation of the KCNT1 gene, a rare disease that causes...
KABC KCNT1 Epilepsy 5-25-23.mp4
KABC KCNT1 Epilepsy 5-25-23.mp4
Local Boy’s Journey With Rare Epilepsy Offers Hope to Others
Local Boy’s Journey With Rare Epilepsy Offers Hope to Others
ONCE UPON A GENE - EPISODE 182 - Doctor and Rare Disease Dad Is On A Mission to Accelerate Research — Once Upon A Gene
ONCE UPON A GENE - EPISODE 182 - Doctor and Rare Disease Dad Is On A Mission to Accelerate Research — Once Upon A Gene
New hope for boy with rare epilepsy who has up to 50 seizures a day | ITV News
New hope for boy with rare epilepsy who has up to 50 seizures a day | ITV News
Three-year-old Paddy from Forest Hall has KCNT1-related epilepsy. The neurological condition is very rare. Around 12 children in the UK known to have it. | ITV News Tyne Tees
Fundraisers for KCNT1
Support our work
Contact Us and Join Our Mailing List
Contact Us and Join Our Mailing List
Connect with us. Sign up, write us or call. Whether you're a parent/caregiver of a KCNT1 patient, a friend or supporter, there's a community here for you.
For KCNT1 parents
Parents: Register to receive our updates
Parents: Register to receive our updates
If you or a loved one is affected by KCNT1 epilepsy, fill out this form to connect with the Foundation and receive personalized support.
Information for families
Information for families
Watch helpful video resources for parents/caregivers of children with KCNT1 epilepsy. Learn, feel supported, and gain clarity from trusted experts and families.
Videos on Vimeo
Videos on Vimeo
Participate in KCNT1 research
Digital Natural History Study with Invitae & Ciitizen
Digital Natural History Study with Invitae & Ciitizen
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