Phone: 800-926-4797 or 941-312-0400
Your membership provides this website - Join Today!

 

HOME

BE INFORMED
  
> About PWS
  
> Get Publications
 
 > About PWSA (USA)
        
Board of Directors
        
Adults with PWS Advisory
       
 Office Staff

MEDICAL
   > Health Concerns
 
 > Medical Alert
  
> Psychiatric
  
> Diet Resources
  
> Growth Hormone

RESEARCH
   >
Research Grants
   >
Funded Research

   > Participants Wanted
   > Research Topics
   > Scientific Advisory Board
   > Clinical Advisory Board

GET INVOLVED
 
  > Spread Awareness
  
> Become member
   >
Registry

SUPPORT
  
 > Newly Diagnosis
   >
Non-Medical

 
 > For Families
  
> For Providers
           
Advisory Board
   >
For Educators

   > State Chapters
   > Links and Resources

MEDIA

GIVE

CONTACT US

 
Recommended for Teens and Adults with PWS and their Parents and Caregivers.

“Prader-Willi Syndrome Is What I have , not Who I am!”

by Janalee Heinemann

Our heartwarming new 70 page book is the first ever collection of writings by people with the syndrome-for others with the syndrome-and for all who want to understand what it is like to live with the syndrome. It is a window into the feelings of all of our young people with PWS-and a light reflecting all of their beauty and courage. This book will be appreciated by all older children and adults with the syndrome, and is a “must” for all caregivers, providers and teachers of our older children.  A PWSA (USA) publication, 2004 70 pages Member cost $10, non-member cost $15 plus shipping. Call our PWSA (USA) office at 1-800-926-4797 to order or Click here to order

 


Return to Home page

PWSA(USA) Disclaimer 

Membership
Payments

PWSA (USA)
Privacy Policy

PWSA (USA) Link Policy

Email PWSA(USA)

 Email Webmaster