The faculty and staff of the Seaver Autism Center for Research and Treatment are pleased to have worked with these patients and families, and we are grateful for their willingness to share their personal stories about autism spectrum disorder and related conditions.
The Whitney family, upon discovering their son had a rare FOXP1 mutation, partnered with the Seaver Autism Center to help better understand FOXP1-related disorder.
The Clayton family has found a second family in the Seaver Autism Center through participating in clinical trials.
Ada Mae’s Journey
In 2014, Ada Mae Grashow was diagnosed with Phelan-McDermid syndrome, a rare genetic condition.
Finding New Hope Through a Clinical Trial
Kali Kurtz was six months old when she began showing symptoms of what would later be identified as Phelan-McDermid syndrome.
The New Normal: What Our Journey with Autism Has Taught Us
The Underwood family was surprised when their daughter Charilyn was diagnosed with autism in 2004.