General Education Meeting Recap by Luis Prado, Administrative Director
The 2026 General Education Meeting was a strong entry in our long line of conferences. This year PWCF returned to
Creating Connections, Confidence, and a Little Glow Along the Way By Melissa Estrada
As a mother of a young child with Prader-Willi syndrome (PWS), I know how important it is to create opportunities
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VYKAT XR Webinar for Professional Providers – Thursday, October 22
Managing Hyperphagia in Prader-Willi Syndrome (PWS) with VYKAT XR (diazoxide choline): A Webinar for Residential Providers will explore key considerations
Golden Year by Shaquinta Prince
Five years ago, when I found out I was pregnant with my daughter, I began to imagine all the possibilities
Recapping the Soleno Community Day in San Jose
The Soleno PWS Community Day at the Children’s Discovery Museum of San Jose was a wonderful gathering. We had 25 parents, family
Recapping the Soleno Community Day in Los Angeles
Soleno’s Community Day took place in Los Angeles on Saturday, July 25. I attended the event in hopes to see
Welcome to the New Website!
Dear PWCF Families, Welcome to the brand new website! We are incredibly excited to introduce you to our user-friendly home
Walking for PWS 2025
Celebrate 25 years of the Walking for PWS events at a city near you! This event series happens once a
A PWS Athlete’s Story
The PWCF Walks are now behind us, and from what I have heard they were once again amazing. This year,
A Chance Encounter
“Nobody is promised tomorrow, stay strong and savor the moment.” – Nichole Broussard Prader-Willi syndrome appears in about every 1