• RARE-X Introduction

    Join Koolen-de Vries Syndrome Foundation and Megan O'Boyle of RARE-X for an introduction to the RARE-X platform. We are very excited about the launch of the KdVS Data Collection Program (DCP). When families contribute data, researchers, doctors and our community can understand more about Koolen-de Vries Syndrome and develop better treatments. This webinar will be […]

  • Webinar with Brooke Latour, KdVS Fellow

    Join the Koolen-de Vries Syndrome Foundation and KdVS Fellow Brooke Latour for an update on her past year of research. Don't forget to register!

  • KdVSF Connect – Kool Family Meet & Greet

    Join the KdVS Foundation for a casual Meet & Greet virtual event! Kool individuals of all ages and their families are welcome to attend! The event takes place September 25, 2022 at 8 pm EASTERN TIME! Not sure what time that is for you? Check your time zone HERE! KdVSF Connect events are a great […]

  • KdVSF Connect – Kool Family Meet & Greet

    Join the KdVS Foundation for a casual Meet & Greet virtual event! Kool individuals of all ages and their families are welcome to attend! The event takes place October 1, 2022 at 12 pm EASTERN TIME! Not sure what time that is for you? Check your time zone HERE! KdVSF Connect events are a great […]

  • KdVSF Connect – Emotional Support Group

    Join the KdVS Foundation for the virtual Emotional Support Group. This support group is for KdVS Caregivers. The event takes place October 23, 2022 at 8 pm EASTERN TIME. Not sure what time that is for you? Check your time zone HERE! KdVSF Connect events are a great opportunity for the KdVS community to join […]

  • KdVSF Connect – Epilepsy Discussion and Support

    In honor of Epilepsy Awareness Month, this month's KdVS Connect revolves around all things KdVS and Epilepsy. This virtual support group is open to anyone interested in the topic and it takes places on Sunday, November 13, 2022 at 8 pm EASTERN. Not sure what time that is for you? Check your time zone HERE! […]

  • KdVSF Connect – Newly Diagnosed Meet & Greet

    Join the KdVS Foundation for a virtual Meet & Greet for newly diagnosed families (diagnosis within the last two years). The event takes place Saturday, December 10, 2022 at 12 pm EASTERN TIME. Not sure what time that is for you? Check your time zone HERE! KdVSF Connect events are a great opportunity for the […]

  • Introduction to Help, Hope, Live

    The KdVS Foundation is proud to partner with Help Hope Live, a trusted medical fundraising nonprofit that supports the rare disease community across the country. Don’t take on out-of-pocket medical expenses alone: trust the nonprofit fundraising experts, and access benefits from one-on-one fundraising help to tax-deductible donations for donors to fundraising that won’t jeopardize your […]

  • KdVSF Connect – Kool Family Meet & Greet

    Join the KdVS Foundation for a casual Meet & Greet virtual event! Kool individuals of all ages and their families are welcome to attend! The event takes place January 7, 2023 at 12 pm EASTERN TIME! Not sure what time that is for you? Check your time zone HERE! KdVSF Connect events are a great […]

  • KdVSF Connect – NEW Emotional Support Group Series

    We are trying something NEW! In the past, the KdVSF Connect Emotional Support group meetings have been very popular. This February, we are offering a small group series of emotional support group meetings. This group will meet four times in the month of February and we ask attendees to commit to attend 3 of the […]