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“First 100 Days”

“First 100 Days”

Welcome to the “First 100 Days of your membership with the Phelan-McDermid Syndrome Foundation.

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Caregiver Support Groups

Caregiver Support Groups

We are thrilled to continue our support group program for Phelan-McDermid syndrome caregivers.

Continue ReadingCaregiver Support Groups
Winter Break Solutions

Winter Break Solutions

by: Carla D'Imperio, Director of Family Support.We gathered your ideas to help make the most of breaks from school and programs.We…

Continue ReadingWinter Break Solutions
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
How are Phelan-McDermid Syndrome and Autism Related?

How are Phelan-McDermid Syndrome and Autism Related?

A large percentage (~75-80%) of people with a Phelan-McDermid syndrome diagnosis also have a diagnosis of autism spectrum disorder. This article…

Continue ReadingHow are Phelan-McDermid Syndrome and Autism Related?
“First 100 Days” Program Updates

“First 100 Days” Program Updates

We started the "First 100 Days" program a year ago and have had 100 US families join our membership in that time. We are so happy to be able to provide our new families with this intensive, personal, and differentiated support.

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Neuropsychiatric Support Group Registration

Neuropsychiatric Support Group Registration

Registration is open for our third support group topic, Coping With Neuropsychiatric Episodes. This support group will be open only to those caregivers in our community who have lost a child or adult with Phelan-McDermid syndrome.

Continue ReadingNeuropsychiatric Support Group Registration
Carter Family Adventures – Our Top Travel Tips

Carter Family Adventures – Our Top Travel Tips

The Carter family shares tips and tricks on how to include your Phelan-McDermid syndrome loved one on family adventures.

Continue ReadingCarter Family Adventures – Our Top Travel Tips
SHANK3 in Phelan-McDermid syndrome

SHANK3 in Phelan-McDermid syndrome

What is SHANK3? SHANK3 is a gene that is important for the development and function of the nervous system. Genes are…

Continue ReadingSHANK3 in Phelan-McDermid syndrome
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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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