The KAT6A families have recently created The KAT6A Foundation, a 501c3 organization to support families coping with this extremely rare disease.  Please visit the Foundation’s website to donate.

The Muller’s also participate in the annual Race for Every Child sponsored by Children’s National Medical Center. We enter a team called “KAT6A Kids” and all funds that our team raises go to support KAT6A research through a dedicated fund at the hospital.

Please consider joining us in the race or in raising funds!