May Is PWS Awareness Month
You Can Help Bring Awareness to Prader-Willi Syndrome!
In 2019, the House of Representatives officially recognized May as Prader-Willi Syndrome Awareness Month, and since then, our community has used this time to share stories, raise awareness, and push for the research breakthroughs our loved ones deserve. Awareness leads to action, and action leads to change.
Small actions spark big change. Educate others about PWS and the urgent need for treatments by:
Prader-Willi syndrome (PWS) is a genetic disorder that occurs in approximately one out of every 15,000 births. PWS affects males and females with equal frequency and affects all races and ethnicities. PWS is recognized as the most common genetic cause of life-threatening childhood obesity.
Watch this short video to learn more about PWS, then click here to learn more >>
If you're a parent or caregiver of a person with PWS, one of the most powerful ways you can drive progress is by participating in the Global PWS Registry. The FDA relies on well-documented data to approve new treatments, and the Registry provides the essential natural history data researchers need. Your participation helps shape the future of PWS care, ensuring that the voices of those living with PWS are heard. Take 10 minutes to complete or update your surveys today! Visit the Registry >>
Sign up for our awareness month emails and you will receive a daily graphic with a PWS-related fact to help spread awareness!
Everything we do, we can do because of YOU. Do you want treatments and a cure for PWS? If so, we invite you to join us and play a vital role by fundraising for PWS research. Fundraise >> or Donate >> to support our efforts.
Need help getting started? Fundraising can be anything you want it to be. Here are a few ways you can get started in minutes!
📱From your device – Launch a page in minutes, then share it! Become a Fundraiser >>
🧡 Host an Orange Day – Collect donations at work or school for the chance to wear orange (or jeans) for the day! Become a Fundraiser >>
🍽 Fast for the 15th – Skip a meal on May 15th and donate what you would have spent to FPWR. Download the Graphic >>
🏆 Move for Research – Run, walk, or cycle as part of our Move for Research campaign! Learn More >>
How Do I Start Fundraising?
No experience necessary! One of the easiest ways to launch a customized fundraising page in minutes is by clicking here >> Become a Fundraiser, or, simply set up a Facebook fundraiser! Check out our fundraising toolkit for templates, customizable graphics, and more!
The Foundation for Prader-Willi Research (federal tax id 31-1763110) is a nonprofit corporation with federal tax exempt status as a public charity under section 501(c)(3).
The mission of FPWR is to eliminate the challenges of Prader-Willi syndrome through the advancement of research and therapeutic development.
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