Thank you for attending our international 2014 conference


By Sue Lomas


Dear Families and Friends,

It was so wonderful to see so many families from so many places at our International Conference in Orlando, Fla. 

Thank you all for making the trip and for the incredible outpouring of love and friendship.I also want to thank the families who could not make it to the conference but were so enthusiastic about watching and commenting on the live streaming of sessions.

Each conference, we see how strong, resilient and caring our group is. Even with all our growth, we continue to believe and nurture our one voice, our one mission: to improve the quality of life for all of our children.
And each conference, our resolve is reinforced. 

Thank you all for being part of it, part of this amazing family.

Best,
Sue
Board President, Phelan-McDermid Syndrome Foundation


_______________________________________________________________________________

 

Our sponsors were key to the conference's success


By Barbara Cruz


Dear PMSF Family,

I would like to offer a sincere thank you to this years conference sponsors and the team of volunteers who gave so freely of their time to make our 2014 conference a success.  Without the generosity and hard work of these individuals our conference would not have been possible.



Gratefully,
Barbara Cruz,
Executive Director
Phelan-McDermid Syndrome Foundation

 

_____________________________________________________________________________________


Largest number of families ever attends PMS conference

By Nick Assendelft
Vice President, Board of Directors


Outstanding. Wonderful. Enriching.

That's how many family members described their experiences at the 2014 Phelan-McDermid Syndrome Foundation International Conference in Orlando, Fla., the largest gathering ever of families affected by Phelan-McDermid Syndrome.

Click Here to Read Full Story

_____________________________________________________________________________________

Last Updated on Monday, 11 July 2016 00:20
 
Copyright © 2017 Phelan-McDermid Syndrome Foundation. All Rights Reserved.