A CURE IS OUT THERE. HELP US FIND IT.
DONATE

  • HOME

  • PCDH19 EPILEPSY

    • ABOUT PCDH19 EPILEPSY
    • PCDH19 EPILEPSY SYMPTOMS
    • NEWLY DIAGNOSED

  • WHO WE ARE

    • ABOUT THE ALLIANCE
    • OUR STORIES
    • OUR TEAM
    • ALLIANCE BLOG

  • RESEARCH

    • RESEARCH INFORMATION
    • RESEARCH GRANT PROGRAM
    • PCDH19 PATIENT REGISTRY
    • ALLIANCE FUNDED RESEARCH
    • ALLIANCE CONFERENCES

  • RESOURCES

    • FAMILY EDUCATION AND SUPPORT VIDEOS
    • SUPPORT
    • BEAR-ERS OF HOPE
    • PCDH19 AT SCHOOL
    • SIBLINGS
    • THE LADYBUG CARD
    • MORE RESOURCES
    • FAQs

  • GET INVOLVED

    • HOW YOU CAN HELP
    • PARENT SUPPORT GROUP
    • FUNDRAISING
    • RUN FOR A CURE
    • PHOTO / MEDIA SUBMISSIONS
    • ALLIANCE WRISTBANDS
    • SHOP THE WEB
    • EVENTS CALENDAR
    • CONTACT

  • More

    Use tab to navigate through the menu items.
    The PCDH19 Alliance is a registered non-profit by the Internal Revenue Service under Section 501 (c)(3). We are 100% volunteer run. All the funds we raise go directly to funding research, supporting families, raising awareness, and finding a cure.

    Copyright 2021 PCDH19 Alliance

    926 A #212 Diablo Ave, Novato, CA 94947

    EIN: 45-4020102

    • Facebook App Icon
    • Twitter App Icon
    • Instagram Social Icon
    Standing by our Sister: The Sibling Impact of PCDH19

    Standing by our Sister: The Sibling Impact of PCDH19

    My First 18 Months as a PCDH19 Dad

    My First 18 Months as a PCDH19 Dad

    Through Claire's Eyes: A Woman's Thoughts on Living with Autism and PCDH19 Epilepsy

    Through Claire's Eyes: A Woman's Thoughts on Living with Autism and PCDH19 Epilepsy