KAT6 Foundation

Dr. Olaf Bodamer shares an open letter with the KAT6 community regarding a new multidisciplinary clinic for folks with genetically confirmed KAT6 related disorders.

Interested? Email rarediseases@childrens.harvard.edu with the requested information.

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Listen in as the Arsenault-Hall family discusses their KAT6 diagnosis and therapy journey.

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Huge thanks to Connections Beyond Sight & Sound, Maryland/DC's DeafBlind Project, and Dr.@jenistepanek for hosting and allowing our families to share their story.

In this interview, KATwalk Co-Chair Katie shines a light on Team Benjamin's KATwalk, taking place Friday!

@SpecialOlympics Unified Champion school @slps_lakers caps off Inclusion Week with a KATwalk to raise funds, awareness and support the Bator family.

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Join @camraredisease on Wednesday, October 7th for a packed program of talks, panels and interactive workshops at #RAREsummit26 - exploring policy, care, health data, partnerships and innovation.

📷 In person or online
📷 Program & tickets: camraredisease.org/raresummit26-p…

KATwalk tees are available in the KAT6 shop!

Whether you're showing your support as you KATwalk ANYWHERE or didn't purchase a tee at registration, we've got you covered! Items can be purchased online and shipped straight to your home!

bonfire.com/store/kat6-fou… @Bonfire