Our journey
From Uncertainty to Advocacy…
Our journey with Angelman syndrome, has been both challenging and incredibly rewarding. Through this video, we hope to share a glimpse into our life, the
August 9, 2024
Our journey with Angelman syndrome, has been both challenging and incredibly rewarding. Through this video, we hope to share a glimpse into our life, the
After two whirlwind weeks of traveling through six states and clocking over 2,100 miles, we’ve finally hit a pause button, giving us a moment to
When faced with a challenging situation, do you see the glass as half empty or half full? Do you choose to pity or to praise?
As parents of a child with special needs, my wife and I often encounter unique challenges that require unique solutions. Our son has Angelman syndrome,
As any parent can attest, the worst thing you ever want is to have to watch your child suffer. Unfortunately, we had no control over
We LIKE to be adventurous … ok, ok … pointing out the key word – like! We traveled to the Philippines in 2017 and it
We have been home since Saturday. I’m not a writer so it’s harder for my creative mind to write on the spot while we are
The mission of the Angelman Syndrome Foundation is to advance the awareness and treatment of Angelman syndrome through education and information, research, and support for
We are beyond grateful to Anker for their generous donation of the Nebula Mini Projector, and it has been a total game-changer for our family!
