This episode features a conversation about Prader-Willi Syndrome (PWS) and the different resources available for families who have a child with PWS. We were joined by Paige Rivard, CEO of the Prader-Willi Syndrome Association of the United States (PWSA-USA), and Dorothea Lantz, PWSA-USA's Community Engagement Specialist.
Contact:
Lisa Ford
lford@arcnj.org
732.828.2022