|WHY SHOULD YOU
PWSA (USA) has credibility and clout.
We know the difference between noisy, activism and quiet, long-term
accomplishment. We are not a start-up organization. Our money goes to
research and member support. PWSA (USA) has a 30-year history of providing
services to families dealing with Prader-Willi syndrome.
We value your time and money.
PWSA (USA) has a strong and ethical not-for-profit accounting system that
assures our organization has the appropriate checks and balances required
by law and good charitable operation standards recommended by the National
Association of Non-Profit Boards and Council of Better Business
We are recognized in the research community.
The professionals on our Medical and Scientific Advisory Boards are
recognized by their peers worldwide. They have access to the latest
scientific data and guide us through the complex world of research.
We offer membership support.
While we continue our fight for a cure for our children, PWSA (USA) will
not forget your loved one’s other needs for support, education and
community awareness. No other organization in the world has the extensive
education and support programs provided by PWSA (USA).
PWSA (USA) is a relatively small group of committed people trying to
serve an ever-expanding population—without federal or state aid. We need
your active support.
Together we will make the sun shine brighter on our
children... and together we will find the CURE!
“I don’t know what your destiny will be, but one
thing I know; the only ones among you who will be really happy are those
who will have sought and found how to serve.”
~ Dr. Albert Schweitzer