Helpful travel tips and resources for families visiting the Kool Klinic from across the U.S. and around the world. For many families in the Koolen-de Vries Syndrome (KdVS) community, traveling […]
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We’re thrilled that a milestone moment is being met for the Koolen-de Vries Syndrome Foundation (KdVSF) and our global community—the very first Kool Klinic is officially opening this April in […]
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October is Cybersecurity Awareness Month — a perfect time to pause and make sure we’re all staying safe on the internet. The online world helps our Koolen-de Vries Syndrome (KdVS) […]
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September is Service Dog Awareness Month; a perfect time to shine a spotlight on the incredible pups who play such an important role in the lives of individuals with Koolen-de […]
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The Back to School season can bring excitement, new opportunities and fresh routines. But for families of children with Koolen-de Vries Syndrome (KdVS), it also comes with unique challenges like, […]
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Becky is sharing her Koolen-de Vries Syndrome (KdVS) story for KdVS Awareness Day - because every story deserves to be seen, heard and celebrated.
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Nothing quite prepares you for the moment you’re told you and your children have a rare genetic syndrome. Koolen-de Vries syndrome wasn’t something I had ever heard of before, let […]
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The time is here! The Koolen de Vries Patient Advocacy Summit will be held in Chicago, IL, USA from July 16th – 18th, 2025. There are so many sessions to […]
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Wow, what a year! Download our 2024 annual report to view a quick snapshot of initiatives we worked on throughout 2024.
READ MORECalling all Kool Adults, Caregivers, Teachers and Healthcare providers! We’re asking for members of our community to meet with our friends over at Medical College of Wisconsin (MCW) who has […]
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