What's new?

Our non-profit association aims to:

  • Raise public awareness on the Phelan-McDermid syndrome in France

  • Provide support to people suffering from a rare disease in France

  • Organize and participate in events to raise funds for research

  • Provide support to families and organise conferences with researchers and Phelan-McDermid doctors

  • Work with and support the International Phelan-McDermid Syndrome Fondation in the USA

FIND ALL OUR LATEST NEWS on our French website by clicking on the top left flag

AND ON OUR SOCIAL MEDIA

  • 22q13 Phelan McDermid France PMS
  • Whatsapp
  • @tehanipms
  • 22q13 Phelan McDermid France PMS
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The Phelan-McDermid Syndrome Foundation launched a new website in French which will enabled French speakers to directly access its many news and other updates!


When you access the website, scroll down to the bottom of the Welcoming page and click on the language menu under "Connect with Us" and "Translate", choose "French". All the website will be translated in French and will make navigating on the Fondation Phelan-McDermid website easier for our members who do not speak English.


Our association is pleases to support and work with the Phelan-McDermid Syndrome Fondation, who has been a pionneer in bringing awareness to the Phelan-McDermid Syndrome and has contributed to many scientific advances on the Syndrome. We have signed a global partnership with the Phelan-McDermid Syndrome Fondation and, every year, we are proud to donate part of our collected funds to the USA Fondation in order to support their international work around the world.


Enjoy the visit on the new Phelan-McDermid Syndrome Foundation website :

https://pmsf.org

Download our report for past activities here