WELCOME TO THE VIRTUAL WALK FUNDRAISING PAGE
Unfortunately, the walk for 2017 had to be postponed to May 20th of 2018. However, you may still donate and collect donations for the chapter through this virtual walk.
We have made it easy for you to register and raise funds for PWSA New England!
Any donation collected outside the Firstgiving website can be documented on the site and collected the day of the walk.
If you would like to donate to a friend's page search for your Friend to the right.
You can also check out the event info here as well or make a general donation by clicking on the "DONATE" button
Prader-Willi syndrome is a complex non-hereditary birth defect resulting from an abnormality on the 15th chromosome. PWS typically causes low muscle tone, short stature if not treated with growth hormone, incomplete sexual development, and a chronic feeling of hunger that, coupled with a metabolism that utilizes drastically fewer calories than normal, can lead to excessive eating and life-threatening obesity, among many other medical and developmental issues. PWS is the most common known genetic cause of life-threatening obesity. Prader-Willi syndrome is a life-long condition and currently there is no cure.
*Prader-Willii Syndrome Association New England is a non-profit organization with a 501(c)(3) status as designated by the IRS and is dedicated to improving and enhancing the lives of everyone affected by Prader-Willi syndrome. This event will benefit both the PWSA New England and PWSA USA National organizations.