A collaboration between the Children’s Hospital of Philadelphia and Penn Medicine offers children and adults with Williams ...

YEAR-OLD Alexandra was born with a rare genetic condition called Williams syndrome. Alexandra describes the condition as ...

Walk4Williams, an event raising funds for the Williams Syndrome Association, will be held Saturday, Oct. 2, at Yucaipa Community Park, 34900 Oak Glen Road. Registration begins at 9 a.m., followed ...

It is the result of the deletion of about 20 genes and affects an estimated 20,000 to 30,000 people in the US, according to the Williams Syndrome Association. People living with the syndrome tend ...

The walk, in support of the Williams Syndrome Association, also will include lunch and music by Mark Proulx. For more information or pledge forms, contact Kerri Kava at (701) 367-8645 or Ann ...

The Williams Syndrome Association was formed in 1982 by, and for, families of individuals with Williams syndrome to provide resources immediately needed and a strong, supportive community for a ...

Christopher Knight is bringing smiles to families across the country with a heartwarming new documentary. Williams Syndrome, first identified by researchers in 1961, is a rare genetic condition ...

Then they found San Antonio’s chapter of the Williams Syndrome Association, or WSA. “I can’t even count how many people we met. I had no idea that we had such a big family here.

The Williams Syndrome Association is having a fundraiser on May 5 in Urbana. Greg Dohler/The Gazette Erin Rupolo and her daughter Sophie, 3, who has Williams syndrome, Monday at their Rockville home.

Williams Syndrome, which affects one in 10,000 worldwide and an estimated 20,000 to 30,000 in the U.S., according to the WSA, is not well-known.

CONCORD, Calif., July 9, 2024 /PRNewswire/ -- The Williams Syndrome Association (WSA) launched their biennial convention today in Phoenix, Arizona. For the first time, the event has a face and her ...