This June, Cisco employees are lacing up their sneakers, hopping on their bikes, and diving into the water to raise vital funds and awareness for Prader-Willi Syndrome Association | USA (PWSA | USA). From challenging bike marathons and invigorating lake swims to community 5Ks, scenic hikes, and adventurous kayaking trips, our teams are pushing their […]
Hosted by the Prader-Willi Syndrome Association of Oregon & Washington All PWS families, physicians, and nurses are welcome to attend a PWS Roadshow event! You'll have the opportunity to meet with other local families, ask the expert panel and connect with PWS professionals in your area, find out about new and potential future treatments for […]
Join host Katie Martinez, mom to Samuel (9, living with PWS) for a fun, high-energy night of music, dancing, and great memories as we move through different decades of music — spending time with friends, family, and community, letting loose, and being part of something meaningful. When: Wednesday, July 15, 2026 | Doors open at […]
A Retreat for Dads of Children Living with Prader-Willi Syndrome When: Friday, July 24 - Sunday, July 26, 2026 Where: Sandia Resort and Casino | Albuquerque, New Mexico CLICK HERE TO LEARN MORE & REGISTER TO ATTEND DADventure is a father-led, independently organized retreat created by Jonathan Andrews and Matt Rivard. This event is a […]
PWS Families in the Pacific Northwest! You're invited to attend PWSA of Oregon & Washington Chapter's PWS Picnic on August 12, 2026. Where: 18206 NE 399 street, Amboy WA 98601 (the same location as previous years) 12-14 free rooms are provided for those coming from out of town at Red-Lion Inn & Suites-Salmon Creek: 13206 […]
Created and hosted by Amy McDougall, mom to Noelle (23, living with PWS), President of the Prader-Willi Alliance of New York CLICK HERE TO LEARN MORE From the PWS Moms' Hiking Weekends Website: The original PWS Moms' Hiking Weekend started with two PWS moms who became hiking buddies, then recognized what a respite their adventures […]
Registration is NOW OPEN! Residential Providers are invited to join PWSA | USA for the 2026 Residential Providers Conference - an unforgettable gathering dedicated to enhancing care, sharing insights, and strengthening community among residential providers in the PWS space. August 21–22, 2026 The Kimpton Brice Hotel | Savannah, GA For the second time, […]
Join the Lens family for a day of golf, good spirits, and great friends as you golf and dine at Heritage Hills Golf Club in Lakeville, MA. This event is celebrating its 17th year raising critical funding for PWSA | USA, an organization that serves individuals living with PWS, their families, caregivers, and more through […]
Hey Nashville! It's time to laugh in rare form. When: Wednesday, September 30, 2026 Where: Zanies Comedy Club | Nashville, TN LEARN MORE AND PURCHASE TICKETS HERE On Wednesday, September 30th, 2026, the iconic Zanies Comedy Club will host the 2nd Annual Prader Silly: A Night of Rare Laughs. This is a one-night-only comedy fundraiser […]
We have reached capacity for the 2026 Moms' Retreat and moved to a waitlist. If you'd like to join the waitlist, please click visit https://cvent.me/ZZPORm. For questions, email afrazier@pwsausa.org. About the 2026 Moms' Retreat Every day, moms and female caregivers in the Prader-Willi syndrome (PWS) community give so much of themselves, often putting their own […]
PWS community! Join PWSA | USA CEO Stacy Ward and her family for an unforgettable evening of support, hope, and community. Hosted at the scenic and historic Brown’s Revolution Hall, this event will bring together families, friends, and supporters for an inspiring evening of cocktails, conversation, and compassion, all aimed at raising awareness and funds […]
PWS Families! You're invited to join the PWSA of Oregon & Washington Chapter for their PWS Christmas & Retreat in Portland, OR. Register here When: Saturday, December 12, 2026 | 2 - 4 PM Where: Oxford Suites Portland – Jantzen Beach 12226 N Jantzen Dr, Portland, OR 97217 Book hotel here Free to Prader-Willi Syndrome […]
Perry A. Zirkel has written more than 1,500 publications on various aspects of school law, with an emphasis on legal issues in special education. He writes a regular column for NAESP’s Principal magazine and NASP’s Communiqué newsletter, and he did so previously for Phi Delta Kappan and Teaching Exceptional Children.
Past president of the Education Law Association and co-chair of the Pennsylvania special education appeals panel from 1990 to 2007, he is the author of the CEC monograph The Legal Meaning of Specific Learning Disability; the more recently published books, A Digest of Supreme Court Decisions Affecting Education and Student Teaching and the Law; and the two-volume reference Section 504, the ADA and theSchools, now in its fourth edition. In 2012, he received Research into Practice Award from the American Educational Research Association (AERA) and the Excellence in Research Award from AERA’s Division A (Administration, Organization & Leadership). In 2013, he received the University Council for Educational Administration’s Edwin Bridges award for significant contributions to the preparation and development of school leaders. In 2016, he received the Education Law Association’s Steven S. Goldberg Award for Distinguished Scholarship in Education Law, and in 2017 he received the Council for Exceptional Children’s Special Education Research Award. Note:Perry’s website is perryzirkel.com
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.
Over the years, as a special-needs parent navigating the Special Education system for Sophie, Jennifer became interested in learning as much as possible about that process. She began by attending PWSA (USA)’s first Wyatt Special Education Advocacy Training in March of 2013, and went on to complete a rigorous 9-month Special Education Advocacy Training course with the Council of Parent Advocates and Attorneys in May of 2015. This included successfully completing an advocacy internship with PWSA (USA). Jennifer is referred school cases by PWSA (USA)’s Family Support Counselors, and then works closely with parents and schools to review education records, assess the child’s situation at school, provide further information about how the syndrome affects the school experience, and, as needed, create improved IEPs and behavioral plans. Jennifer was excited to take on this role of helping parents in the PWS community to work collaboratively with school professionals and parents to create positive, effective learning environments for children with PWS across the country. Jennifer is a graduate of the WSEAT program.
Dr. Amy McTighe is the PWS Program Manager and Inpatient Teacher at the Center for Prader-Willi Syndrome at the Children’s Institute of Pittsburgh. She graduated from Duquesne University receiving her Bachelor’s and Master’s degree in Education with a focus on elementary education, special education, and language arts.
She obtained her PhD from Capella University in Education focusing her research on Prader-Willi Syndrome. Dr. McTighe is also a graduate of the William & Mary Law School’s Institute for Special Education Advocacy. Dr. McTighe is currently the chair of the Special Education Advisory Board for the Prader-Willi Syndrome Association-(USA). Amy is the Chair of PWSA (USA)’s Special Education Advisory Board.
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 Program (IEP) consultant. Staci collaborates with the PWS multi-disciplinary clinic at the Children’s Hospital in Denver supporting families and school districts around the United States with their child’s Individual Educational Plan.
Staci Zimmerman has lived in Denver, CO for the past 17 years. She lives with her husband and 5 year old daughter. Staci attended The University of Kansas, with a B.A in sociology and an M.ed in Special Education, with an emphasis in Autism Spectrum Disorder. Staci enjoys teaching fitness classes, and keeping a healthy, active lifestyle in Colorado.
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.
Before founding SDLC, Jim was the Executive Director of Advocacy, Inc., the Texas Protection and Advocacy program from 1989-2001. During that period, he managed the growth of the program from 34 staff to a staff of 94 and from a centralized operation with one office to a regionalized operation with eleven offices spread across Texas.
From 1981-1989, Jim worked for the Advocacy Center for the Elderly and Disabled (Louisiana’s Protection and Advocacy program) as its Legal Director. From 1979 to 1981 Jim worked as a staff attorney for the Louisiana Center for the Public Interest.
Jim graduated from Tulane University School of Law in 1977, and has a BA in Accounting & Economics from the University of Puget Sound.
Jim is the author of publications and training materials on the IDEA, the ADA, and Section 504, including: Keeping Students with Disabilities in School: Legal Strategies and Effective Educational Practices for Preventing the Suspension of Students with Disabilities – A Resource Manual (2014); Stopping the Schoolhouse to Jailhouse Pipeline by Enforcing Federal Special Education Laws (2006), co–authored with Rhonda Brownstein from the Southern Poverty Law Center.
Jim has served as lead or co-counsel in several major IDEA actions in Texas, Louisiana, and Mississippi on behalf of thousands of students with disabilities, including Angel G. v. Texas Education Agency; Luke S. v. Louisiana Department of Education and Mattie T. v. Mississippi Department of Education. The past decade, he also filed and favorably settled five systemic administrative complaints in Louisiana, Mississippi, and Florida. These systemic complaints were filed under IDEA’s state complaint procedures.
Jim has also made over two hundred presentations at statewide, regional and national conferences on IDEA, Section 504, and ADA issues. The past four years he has also served as one of the faculty members at William and Mary Law School’s week long Institute on Special Education Advocacy.
