Welcome to the Prader-Willi Syndrome Missouri Association website. We're glad you took the time to look at our site and hope you visit us again.

PWSMA's Mission Statement

To achieve a positive difference in the quality of life for children and
adults with Prader-Willi Syndrome and their families.

Our Visions

  • WE BELIEVE  the individual with PWS is first and foremost a human being.

  • WE BELIEVE  in respect for those individuals with PWS and their
    families.

  • WE BELIEVE  a firm, positive and consistent attitude towards both
    behavior and weight management are critical for individuals with PWS to have a quality of life - something which was previously thought impossible.

  • WE BELIEVE  we are a learning Chapter that values communication,
    contributions, teamwork and problem solving from one another in order to provide those individuals with PWS the chance to live happy, healthy and productive lives.

  • To further the mission and programs of the national association,
    PWSA (USA).

  • To promote the ongoing work necessary to guarantee a fulfilling
    lifestyle for children, teenagers and adults with PWS by supporting medical research, education and individualized residential living arrangements.

  • To provide parents and caregivers with a national and international network of information, support services and research endeavors to expressly meet the needs of those individuals with PWS.

  • To increase community awareness of PWS in the State of Missouri.

Welcome! You are the Hit Counter visitor to our website.

Contact Us:

Prader-Willi Syndrome Missouri Association
PO Box 410252
Creve Coeur, MO 63141
(314) 935-9358
whitmanb@slu.edu

 

Disclaimer:

The PWSA of MO web site is intended to provide information only - not to diagnose or advocate particular treatment options. The Diagnosis of Prader-Willi Syndrome should be made through a qualified medical professional. Individuals should only make decisions about treatment options in close collaboration with their own health care team of professionals. Thus, it is strongly urged that patients do not change treatment without first consulting their physician.
The inclusion of any resource or link in the PWSA of MO Web Site does not imply endorsement.
If you have any questions, please write the Prader-Willi Syndrome Missouri Association.