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Endure4Eden: A 24-Hour Golf Challenge to Support the Phelan-McDermid Syndrome Foundation

Endure4Eden: A 24-Hour Golf Challenge to Support the Phelan-McDermid Syndrome Foundation

We are excited to announce the upcoming Endure4Eden fundraiser, organized by Philip Robertson and his team, to support the Phelan-McDermid Syndrome…

Continue ReadingEndure4Eden: A 24-Hour Golf Challenge to Support the Phelan-McDermid Syndrome Foundation
PHELAN LUCKY Sets Sights on $1 Million Goal

PHELAN LUCKY Sets Sights on $1 Million Goal

Over the past decade, more than 59,000 PHELAN LUCKY shirts have found homes in 33 countries across the globe. This has not only…

Continue ReadingPHELAN LUCKY Sets Sights on $1 Million Goal
Katy & Sue’s Birthday

Katy & Sue’s Birthday

We are thrilled to invite you to join us in celebrating a momentous milestone - the 70th birthdays of two INCREDIBLE…

Continue ReadingKaty & Sue’s Birthday
Team Matthew Luis – Dinner & Raffle Fundraiser

Team Matthew Luis – Dinner & Raffle Fundraiser

The Castillo family of Miami, FL held their 6th annual #teammatthewluis dinner and raffle fundraiser and raised over $18,000.00!

Continue ReadingTeam Matthew Luis – Dinner & Raffle Fundraiser
Family Fundraiser: Turner’s Tribe

Family Fundraiser: Turner’s Tribe

by Brooke Turner Jones, Mom to TurnerWe are excited about the prospects of PMS Awareness Day 2023, as it will be…

Continue ReadingFamily Fundraiser: Turner’s Tribe
Phelan Lucky 2022 Is Here!

Phelan Lucky 2022 Is Here!

Phelan Lucky 2022 is an online campaign that takes place for a strict 22-day period—from Jan. 2, 2022, through Jan. 24, 2022! It’s also the only time of year to get your hands on the coveted “Phelan Lucky” T-shirt.

Continue ReadingPhelan Lucky 2022 Is Here!
Turner’s Tribe

Turner’s Tribe

We received Turner's diagnosis in June of 2019. He was 6 years old, and to say we were devastated at first…

Continue ReadingTurner’s Tribe
Cecilia’s Advice

Cecilia’s Advice

Cecilia’s Advice was born out of that deep commitment to fostering research and family support for the thousands of families worldwide affected by PMS.

Continue ReadingCecilia’s Advice
TeamMatthewLuis

TeamMatthewLuis

#TeamMatthewLuis When our sweet and beautiful five year old son, Matthew Luis Castillo, was diagnosed with Phelan McDermid Syndrome it was…

Continue ReadingTeamMatthewLuis
Hope for 22q13 Gala

Hope for 22q13 Gala

When our son Anthony was diagnosed back in July of 2015 at the age of 15 months, we were, as all…

Continue ReadingHope for 22q13 Gala
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Copyright © 2024 Phelan-McDermid Syndrome Foundation. All rights reserved. Any information provided to members or the general public is provided for educational purposes only, and is not intended to replace professional advice from doctors or therapists.

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