It's Empowered Wednesday! Constança is swingin' in to say THANKS! Her family was able to purchase a swing through the Empowered Grant program and can be seen here using it during an occupational therapy session! kat6a.org/empowered-gran…

Have you ordered your KATwalk shirt?? This year, KATwalk shirts are sold separately and are available through our Custom Ink fundraiser. Adult and youth sizes and international shipping available! 🚨 The deadline to order is AUGUST 14th! 🚨 customink.com/fundraising/ka…

One of our families is in the hospital after losing everything in a house fire. Please consider donating to help cover medical costs. Waconia Brewing Co. gofundme.com/f/dru-and-chri…

Check out Peter's team's fundraising page - donate.kat6a.org/fundraiser/482…

Today's team is Peter's Virtual Walk Team! Peter was diagnosed in 2016, and in the years that followed, his parents started this foundation and worked with National Organization for Rare Disorders (NORD) to develop a patient registry to identify cases and find a treatment. donate.kat6a.org/team/517357 Natacha Esber

Check out this article on the research being done at the #ArboledaLab using #iPSCs and #cerebralorganoids David Geffen School of Medicine at UCLA #AileenNava Valerie Arboleda MD, PhD 🤷🏻‍♀️

donate.kat6a.org/team/517357

This weekend, Niagara Falls were lit in KAT6 colors in honor of our families and foundation. It was simply magic ✨ My favorite pic is our KAT6 kiddo Toby taking a peek through the binoculars Niagara Falls Canada Niagara Parks

We invite you to our upcoming webinar, "Early Treatment Pathways for Children with Neurodevelopmental Disabilities." This event will take place on October 11, 2023, at 8:00 PM (US, EST) and October 12th at 11:00 AM (AEST). form.typeform.com/to/ZoDWKJn2

This webinar is a great opportunity to gain insights and understanding from esteemed experts in the field of neurodevelopmental disabilities. Our speakers are leaders in their respective areas of expertise; presentations to be followed by a Q&A. form.typeform.com/to/ZoDWKJn2

The 5th Int’l KAT6 Conference will be held on June 8, 2024 in Baltimore, MD and offers our families a chance to connect, participate in research and meet with medical specialists. We hope you’ll join us! Register today! kat6a.org/5th-annual-kat…

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Our sweet Patrick 🥹🎻🥰🦓🎄

Merry Christmas from the KAT6 Foundation!

Join us for the KAT6 Conference! This conference supports individuals and families living with KAT6 and enables open dialogue between families, clinicians and researchers. Rooms at the group rare are limited - register ASAP. kat6a.org/5th-annual-kat… Natacha Esber Angie Serrano

In November 2022, the first project directly funded by our foundation reached publication in Genes MDPI. The work done by JOSE ANTONIO SANCHEZ and his team allow us to move forward on the path toward treatment for those living with KAT6 syndromes. Read in full 👉kat6a.org/the-first-kat6…

Join us for the 5th Int'l KAT6 Conference! Our conference supports KAT6 families with the goal to solidify KAT6A and KAT6B research internationally and facilitate open dialogue between families, clinicians and researchers. Registration is required. kat6a.org/5th-annual-kat…

The KAT6 community came together in Baltimore, MD for the 6th International Conference - two powerful days of connection, research, and inspiration. Click the link to watch the highlight video created for us by Jeff Worden: youtu.be/p1hqdczwwZg

Team Peter's KATwalk features live music, fishing and a walk in the park! This year features a new t-shirt design, available with the purchase of a "KATwalk Admission with T-shirt" ticket. KATwalk Anywhere teams can order thru our Custom Ink fundraiser. customink.com/fundraising/ka…