May is #PWSAwareness Month | We Have Your 2018 Awareness Resources

may-is-pwsawareness-month-we-have-your-2018-awareness-resourcesVisit our 2018 PWS Awareness month page on the FPWR website for inspiration, educational resources and fundraising ideas to help you with your awareness activities! And don't forget to sign up for our PWS Awareness Month emails to receive a daily PWS fact that you can share to help build awareness.

Awareness Resources All Month Long

On the PWS Awareness Month page, you'll find videos, downloads, and social media graphics to share with the hashtag #PWSAwareness, and stories of hope from parents, friends, and caregivers. The page lists and links to the many One SMALL Step walks, golf tournaments, and other fundraising events organized by FPWR's amazing PWS community, with information to help advocates launch their own fundraiser easily online.

PWS Awareness Month Background

Introduced by Reps. Ed Royce (R-CA) and Jane Harman (D-CA), the House of Representatives passed House Resolution 55 on December 8, 2009. The resolution established May as an awareness month for Prader-Willi syndrome (PWS).

Facebook Profile Frames

"This important resolution marked a real turning point in the fight against PWS," said Lauren Schwartz Roth, Ph.D., former President of the Foundation for Prader-Willi Research (FPWR). "In addition to establishing an awareness month, the resolution recognizes the importance of awareness and early diagnosis and recognizes the efforts and commitment of patient advocacy groups such as the FPWR. We are deeply appreciative to Reps. Royce and Harman for their hard work and support."

For more information on PWS Awareness Month, download the PWS Awareness Month news release here.

VISIT THE #PWSAWARENESS WEB PAGE

Topics: News

Susan Hedstrom

author-image

Susan Hedstrom is the Executive Director for the Foundation for Prader-Willi Research. Passionate about finding treatments for PWS, Susan joined FPWR in 2009 shortly after her son, Jayden, was diagnosed with Prader-Willi Syndrome. Rather than accepting PWS as it has been defined, Susan has chosen to work with a team of pro-active and tireless individuals to accelerate PWS research in order to change the natural history of PWS. Inspired by her first FPWR conference and the team of researchers that were working to find answers for the syndrome, she hosted her first One SMALL Step walk in 2010 and began the development of the One SMALL Step walk program which now raises over $1.5 million a year for PWS research.

PWS Blog Subscribe