We are extremely grateful toย YOU, our PWS community, for supporting PWSA | USA on Giving Tuesday! A special thank you to our generous anonymous donors who are matching gifts dollar for dollar up to $38,500 through December 31st.
Know that your donations will make a direct impact on the lives of those living with PWS and their families, and will support Advocacy, Family Support, and Research initiatives in the new year.
IT'S NOT TOO LATE to make your Angel Drive donation at the button below and take advantage of this year's generous match!
It has been said that each of us needs just three things to be truly happy in this world: someone to LOVE, something to HOPE for, and something to DO. Together with our Prader-Willi syndrome community near and far, our mission requires all three.
WE LOVE: They are our children, our grandchildren, nieces, nephews, aunts, uncles, neighbors, patients, and friends living with the obstacles that come with this rare and complex diagnosis of PWS.
WE HOPE: We unite in hope to transform those efforts into opportunities for our loved one that leads to a life filled with possibility. We move forward each day with positivity and determination because we know with certainty that our loved one with PWS has a bright future ahead, despite the challenges they face.
WE DO so much from the moment our loved one with PWS enters the worldโฆ
Help us Continue Building our Angel Drive Thread of Hope!
This holiday season, we invite you to share your HOPE for your loved one with PWS (or the PWS community) when you fill out our online donation form. Why? Because your message of hope will become part of a thread connecting all of us near and far as we begin a new year. Share what your HOPE is for 2023 when you fill out the Angel Drive donation form.
Hear how individuals living with PWS and their families are directly impacted by your gift.




Perry A. Zirkel has written more than 1,500 publications on variousย aspects of school law, with an emphasis on legal issues in special education.ย He writes a regular column for NAESPโsย Principalย magazine and NASPโsย Communiquรฉย newsletter, and he did so previously forย Phi Delta Kappanย andย Teaching Exceptional Children.
Jennifer Bolander has been serving as a Special Education Specialist for PWSA (USA) since October of 2015. She is a graduate of John Carroll University and lives in Ohio with her husband Brad and daughters Kate (17), and Sophia (13) who was born with PWS.
Dr. Amy McTighe is the PWS Program Manager and Inpatient Teacher at the Center for Prader-Willi Syndrome at the Childrenโs Institute of Pittsburgh. She graduated fromย Duquesne University receiving her Bachelorโs and Masterโs degree in Education with a focus on elementary education, special education, and language arts.
Evan has worked with the Prader-Willi Syndrome Association (USA) since 2007 primarily as a Crisis Intervention and Family Support Counselor. Evans works with parents and schools to foster strong collaborative relationships and appropriate educational environments for students with PWS.
Staci Zimmerman works for Prader-Willi Syndrome Association of Colorado as an Individualized Education Programย (IEP) consultant. Staci collaborates with the PWS multi-disciplinary clinic at the Childrenโs Hospital in Denverย supporting families and school districts around the United Statesย with their childโs Individual Educational Plan.
Founded in 2001, SDLC is a non-profit legal services organization dedicated to protecting and advancing the legal rights of people with disabilities throughout the South. It partners with the Southern Poverty Law Center, Protection and Advocacy (P&A) programs, Legal Services Corporations (LSC) and disability organizations on major, systemic disability rights issues involving the Individuals with Disabilities Education Act (IDEA), Americans with Disabilities Act (ADA), and the federal Medicaid Act. Recently in November 2014, Jim retired.