Thank you for supporting your loved ones with KCNT1-related disorders this National Rare Disease Day on February 28th! Just like a zebra’s stripes, every child’s journey with a rare disease is unique. KCNT1 may be labeled "rare," but every month we connect with new families receiving this life-changing diagnosis. Together, we are showing the world that KCNT1 is not so rare after all.
Your gift — no matter how small — makes an incredible impact. By raising awareness and funding our mission, you are helping to support families, drive research forward, and bring us closer to discovering treatments and, one day, a cure.
Every act of kindness brings us closer to a brighter future for kids like Emmy. Just like zebras in a herd, we stand stronger together. From the bottom of our hearts, thank you for making a difference!
Organized by KCNT1 Epilepsy Foundation
501(c)(3) Public Charity · EIN 84-2748218
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