Skip to content
  • 2026 Conference
  • CAREGIVER SUPPORT
  • QUICK RESOURCES
  • PODCAST
  • CONNECT: Family Support
    • New Diagnosis
    • Support Programs
      • Family Support
      • First 100 Days
      • Caregiver Support Groups
    • 2026 Conference
    • Family Stories
    • Resource Library
  • CARE: About PMS
    • What is Phelan-McDermid Syndrome?
    • How Phelan-McDermid Syndrome is Diagnosed
    • Medical Issues & Clinical Care
    • PMS Neuropsychiatric Consultation Group – ECHO
    • Genetic Counselors
    • PMS By The Numbers
  • CURE: Research
    • Strategic Priorities
    • Funded Research
      • Research Grants Program
    • Family Participation Opportunities
      • Participation in Research
      • Clinical Trials in Phelan-McDermid Syndrome
    • Drugs In Development
    • For Research Partners
    • PMS DataHub
  • Foundation
    • About Us
    • Our History
    • Leadership
    • Our Financials
  • Get Involved
    • Fundraise
    • Phelan Lucky
    • Advocate
    • Events
    • Volunteer
  • News & Updates
  • Contact Us
  • CONNECT: Family Support
    • New Diagnosis
    • Support Programs
      • Family Support
      • First 100 Days
      • Caregiver Support Groups
    • 2026 Conference
    • Family Stories
    • Resource Library
  • CARE: About PMS
    • What is Phelan-McDermid Syndrome?
    • How Phelan-McDermid Syndrome is Diagnosed
    • Medical Issues & Clinical Care
    • PMS Neuropsychiatric Consultation Group – ECHO
    • Genetic Counselors
    • PMS By The Numbers
  • CURE: Research
    • Strategic Priorities
    • Funded Research
      • Research Grants Program
    • Family Participation Opportunities
      • Participation in Research
      • Clinical Trials in Phelan-McDermid Syndrome
    • Drugs In Development
    • For Research Partners
    • PMS DataHub
  • Foundation
    • About Us
    • Our History
    • Leadership
    • Our Financials
  • Get Involved
    • Fundraise
    • Phelan Lucky
    • Advocate
    • Events
    • Volunteer
  • News & Updates
  • Contact Us
Join
Donate
  • 2026 Conference
  • CONNECT: Family Support
    • New Diagnosis
    • Programs
      • Family Support
      • “First 100 Days”
      • Caregiver Support Groups
    • Family Stories
    • Resource Library
  • CARE: About PMS
    • What is Phelan-McDermid syndrome?
    • How PMS is Diagnosed
    • Medical Issues & Clinical Care
    • PMS Neuropsychiatric Consultation Group – ECHO
    • About Genetic Counseling
    • PMS By The Numbers
  • CURE: Research
    • Strategic Priorities
    • Funded Research
      • Research Grants Program
    • Family Participation Opportunities 
      • Participation in Research
      • Clinical Trials
    • Drugs In Development
    • For Research Partners
    • PMS Datahub
  • Foundation
    • About Us
    • Our History
    • Leadership
    • Our Financials
    • PMSF News
    • Contact Us
  • Get Involved
    • Fundraise
      • Phelan Lucky
    • Advocate
    • Events
    • Volunteer
  • Join
  • Donate
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!
PMSF Research Roundup: January 2022

PMSF Research Roundup: January 2022

Do you wonder how a research publication affects your loved one or the field of Phelan-McDermid research?The Research Roundup is a…

Continue ReadingPMSF Research Roundup: January 2022
Jaguar Gene Therapy Will Target SHANK3 for Gene Therapy

Jaguar Gene Therapy Will Target SHANK3 for Gene Therapy

JAG201 is designed to address mutation or deletion of the SHANK3 gene, a leading autism candidate gene, by delivering SHANK3 gene replacement therapy.

Continue ReadingJaguar Gene Therapy Will Target SHANK3 for Gene Therapy
PMSF Research Roundup: December 2021

PMSF Research Roundup: December 2021

Do you wonder how a research publication affects your loved one or the field of Phelan-McDermid research?The Research Roundup is a…

Continue ReadingPMSF Research Roundup: December 2021
Hope for Punya

Hope for Punya

https://youtu.be/NmZOnH7tpBk Punya is diagnosed with Phelan-Mcdermid syndrome and does not currently speak. Ananya, her sister, is dedicated to learning how Punya communicates…

Continue ReadingHope for Punya
Research Roundup – September 2021

Research Roundup – September 2021

Do you wonder how a research publication affects your loved one or the field of Phelan-McDermid research?The Research Roundup is a…

Continue ReadingResearch Roundup – September 2021
Shannon’s Birthday

Shannon’s Birthday

Happy 21st B-Day Shannon!Dear Friends and Family,As impossible as it seems, we are celebrating Shannon’s 21st birthday this month. In honor…

Continue ReadingShannon’s Birthday
Phelan-McDermid Syndrome Website Update

Phelan-McDermid Syndrome Website Update

by Diane Linnehan, PMSF Director of Operations The new PMSF website launched on August 11th! With the help of our amazing…

Continue ReadingPhelan-McDermid Syndrome Website Update
Research Roundup, August 2021

Research Roundup, August 2021

A monthly digest of publications regarding Phelan-McDermid syndrome. by Kate Still, Ph.D., PMSF Scientific Director A push towards Whole Genome Sequencing…

Continue ReadingResearch Roundup, August 2021
Maria runs for John

Maria runs for John

We are so thankful to Maria Punzo, who recently completed the Queens Half Marathon in honor of her nephew, John Welsh.…

Continue ReadingMaria runs for John
  • Go to the previous page
  • 1
  • 2
  • 3
  • 4
  • 5
  • 6
  • …
  • 8
  • Go to the next page

Contact Us

8 Sorrento Drive, Osprey, FL 34229

phone: 941-485-8000

fax: 941-220-6605

email: info@pmsf.org

Tax ID: 04-3673104

Engage With Us

  • News & Blog Posts
  • Resource Library
  • Events
  • Website Feedback
  • Join Our Membership

Connect With Us

Facebook-f Twitter Youtube Instagram

Translate

Financial Conflict of Interest

Privacy Policy

Charity Disclosures
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.

Log in

Become a part of our community!
Forgot your password? Get help

Reset password

Recover your password
A password reset link will be e-mailed to you.
Back to
Login
×
Close Panel

By continuing to use this website, you consent to the use of cookies in accordance with our Cookie Policy.

Accept