By Christina Calloway PNT senior writer email@example.com Published: Thursday, May 16th, 2013
A person of few words, Sarah Walker’s action speaks volumes about her passion to help others.
The smiles on the faces of individuals with Angelman syndrome (AS) belie a life marked by severe developmental delay, speech difficulties, seizure disorders and more. And yet, they go on
With much love, I am proud of the Angelman Syndrome Foundation. If you can help them, and families with this condition, please consider donating to them at…
Ben Philpot of the University of North Carolina at Chapel Hill discusses his project to screen for compounds that can reactivate the silenced MECP2 gene as a…
For I know the plans I have for you, declares the Lord, plans to prosper you and not to harm you, plans to give you hope and a future. Jeremiah 29:11. The firs
The Club Deportivo Guadalajara supports Angelman Syndrome Association by collecting used mobile phones and tablet in the official club shop
What we need is more people who specialize in the impossible.’ ~ Theodore Roethke. On the 9th of April 2013, aged 16 months Lily was diagnosed with Angelman … http://www.youtube.com/watch?v=i5dDH6tgIws
CHELMSFORD — A benefit walk at the high school Saturday, May 18, will help raise awareness of a neurological disorder called Angelman syndrome, as well as for medical research, education and support. Angelman syndrome affects 1 in 15,000 people, ..
Melissa Winger blogs about her son Will who has been diagnosed with Angelman Syndrome. It’s such a rare diagnosis that she wants to educate as many people as she can about its existence and how she’s coping with the challenges it brings.
Masked vigilantes will descend upon Baraboo High School this Saturday, bent on battling Angelman syndrome.
Students took a walk down memory lane by reliving their prom days for a good cause. All proceeds went to support Angelman syndrome.
A relatively little known disorder known as Angelman Syndrome is drawing focus in the medical world.
Ravalli Republic Angelman Syndrome is a rare neuro-genetic disorder that occurs in 1 in 15000 live births. …Angelman Syndrome is characterized by a happy demeanor,
Angelman Syndrome – A look at my Friends Tina & Jace. posted in Angelman Syndrome, Children, children parks family, Families, Uncategorized …
Pamela Lyman had never heard of Angelman Syndrome before her son was diagnosed at 15-months-old. Lyman has learned a lot about the disorder in the last 11 years, but her son is teaching her that he’s “just fine.”
Logan, from Ballywalter in Co Down, has Angelman Syndrome, a rare genetic disorder which causes severe learning difficulties and leaves him unable to speak.
Conrad Lyman, 11, navigates down the stairs at home with the help of his grandmother, Jean Blumenauer. Angelman syndrome makes coordination a challenge …
READER SUBMITTED: Aiello Basketball Charity Winner
The Angelman Syndrome Foundation is glad he did. Based on his selections of the final four, and choosing Louisville to win the national championship, …
Yogapalooza to raise money for Fort Bend girl with rare disorder
… a 16-month old Pecan Grove girl who was diagnosed with Angelman’s Syndrome in March. “Angels”, as they are called because of their angelic demeanor, …
Ethan dedicates this song to his little brother with Angelman Syndrome.
Made possible by a grant from the Foster Family Foundation, an organization that has been very generous in supporting the ASF’s mission, the iPads for AS program will provide up to 100 iPads to families that qualify based on financial need.