Season Greetings Everyone and A Happy New Year!
“One of the most critical components of PWSA (USA) support is the medical coverage. Parents and professionals call daily with anything from a medical question to a serious medical crisis. Support and information is provided via phone, information is emailed and faxed, and consultation is provided by members of the PWSA (USA ) Clinical Advisory Board when needed“
-Janalee Heinemann, Director of Research & Medical Affairs-
The clock is ticking and we’re still $48,100 short of our goal to raise $100,000 by tomorrow night. A shortfall like this could impact our ability to provide critical medical coverage for children, adults and families with PWS in the coming months.
If you believe that every person with PWS deserves to reach their full potential…if you’re not willing to stand by while kids go undiagnosed…you can help right now.
Tomorrow is the last day to make your year end donation for 2013. Please don’t let us start the New Year without your support. A child’s life depends on it.
-Ken Smith, Executive Director, Prader-Willi Syndrome Association (USA)