• Skip to primary navigation
  • Skip to main content
  • Skip to footer
Logo
  • Home
  • Understanding KCNT1
  • Parents & Caregivers
    • Newly Diagnosed
    • Early-Onset KCNT1 Epilepsies
      • Medications for Early-Onset Epilepsies
    • Sleep-Related Hypermotor Epilepsy (SHE)
    • Symptoms & Treatments Overview
    • Treatment Approaches
    • Genetics 101
    • Life Expectancy & Long-Term Planning  
    • Financial & Caregiving Tools
    • Support & Resources
    • Sign Up for Our Parent Contact Form
    • Share Your KCNT1 Story
    • Find a Doctor
    • World Map (Census)
  • Professionals
    • Clinicians
    • Industry
    • Researchers
      • Biospecimens
      • KCNT1 Funding
      • Publications
  • Research & Clinical Trials
    • Parents & Caregivers
    • Clinical Trials
    • Clinical Trial Educational Resources
  • Support Us
    • Get Involved
    • Ways to Give
      • Shop our Store
      • Host a Fundraiser
  • About Us
    • Our Mission
    • Our Team
    • Our Advisors
    • Our Approach
    • Our Partners
    • Our Families
  • News & Events
    • FDA Patient Session
    • KCNT1 Remembering Day: October 21
    • News
    • Newsletter
    • KCNT1 in Orlando
    • Past Conferences
      • KCNT1 Anaheim Family Conf
      • Million Dollar Bike Ride
  • Contact
  • D♡nate

KCNT1 Epilepsy Foundation Chosen as a CURE Epilepsy Grant Partner to Support a KCNT1 Research Grant

May 20

The KCNT1 Epilepsy Foundation was selected for an opportunity to potentially fund a $100,000 Rare Epilepsy Partnership Award in partnership with CURE Epilepsy, the leading nongovernmental agency fully committed to funding research to find the cure for all epilepsies. CURE Epilepsy and the KCNT1 Epilepsy Foundation will be joint partners, co-funding this research grant to accelerate progress on our research priorities, doubling the dollars and reach of our Foundation. This request for proposals will include 3 potential research directions: two intended to follow on the heels of new reports linking KCNT1 to traumatic brain injury-induced epilepsy, and linking KCNT1 to the other rare channelopathies SCN1A and SCN8A; and one to follow on the KCNT1 caregiver-reported phenomenon linking a reduction in seizures to episodes of fever. We thank our generous donors, as their contributions allow us to pursue greater co-funding opportunities which can lead to foundational research that helps us understand this devastating form of epilepsy.

Bringing Together the International KCNT1 Research Community

KCNT1 Families meet with the FDA in a Patient Listing Session

Footer

fluid-image
Donate Today
  • Parents & Caregivers
  • Researchers & Professionals
  • About Us
  • Contact
  • Subscribe
Gold 2025 Candid Seal
GAA Member Badge
Citizen Health Proud Partner 2025 Website Badge

Privacy Policy

© 2023 KCNT1 Epilepsy Foundation | All Rights Reserved | Disclaimer

EIN 84-2748218

Copyright © 2026