Please take a moment to read a brief overview of fundraising at the KAT6 Foundation.
KAT6 Foundation Brochure – Revised Oct 2023 – Click here to download.
Download Information Packet from rarediseaseday.org
Our KAT6 community is made up of many dedicated parents who advocate tirelessly for their loved ones. Recently, Kerrie, mother of a child diagnosed with KAT6A syndrome, was able to make a positive impact in her UK neighborhood for children with disabilities. Due to Kerrie’s perseverance, a playground in her local community is now more […]
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Interested in newborn health? Learn about the GUARDIAN Study! The GUARDIAN Study is a free research study screening newborns for rare conditions not covered by standard tests. Early diagnosis can help start treatment as soon as possible. Your choice to participate won’t affect standard screening. Your baby’s results are confidential. Sign up after birth or […]
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Tilly Collins is in the third year of her speech and language therapy degree, studying at Cardiff Metropolitan University, UK. Collins is interested in hearing your thoughts, opinions and experiences of speech and language therapy as parents of children with KAT6A syndrome. Your involvement will be a 30-minute casual interview over the phone or a […]
Read MoreHelp us support people and their families living with KAT6A and KAT6B syndromes. Your donations will fund vital research into KAT6A and KAT6B gene mutations and provide assistive equipment, technology, and therapies to families through our Empowered grants. All donations are tax deductible in the US and go to KAT6 Foundation, a nonprofit 501(c)(3).
