One thing about the kid – he experiences joy in ways that I cannot fathom. Playing with a puppy, enjoying a game of hide and seek, or just getting his favorite girl scout cookie can make Finn downright joyful. It is pretty inspiring. Frankly, he has seemed a lot happier recently. There are pro…
I believe I had a chance to positively influence a child’s life today. I might have had a real impact. But I am afraid that I blew it, and that makes me sad. It occurred while we were taking a walk along one of the hiking trails in Palos Verdes. About thirty minutes into the walk, we ran acros…
Evan -7, AS, self Stimulatory behavior. Has been biting his lip. The chewy tube helps divert his self injurious behavior.
A local family who is reaching out to children with special needs is taking their support group for those with Angelman Syndrome a step further.
By Taylor Smith, The Oregonian Pamela Jean Lyman hugs her son Conrad, 11, who was diagnosed with Angelman Syndrome when he was 15 months old.
The Angelman Syndrome Foundation 2013 National Walk will be held on … In 2007 their son Gabriel was diagnosed with Angelman Syndrome at the age of twelve
Rio Vacary, aged two, suffers the rare genetic condition Angelman Syndrome which means he needs round-the-clock support from mum Gemma and dad Wayne. Gemma said her eldest sons Cody, eight, and five-year-old Jadyn, have had their young lives