Rare but strong. Rare but resilient. Rare but never alone. This Rare Disease Day (Friday, February 28, 2025), we’re standing with the Prader-Willi syndrome community and the 30 million Americans living with a rare disease. Whether you’re sharing your story, spreading awareness, or fundraising for a brighter future, YOU can make a difference. Download our […]
We invite the PWS community to join us for a FREE and important webinar with Harmony Biosciences on Tuesday, March 11, 2025, at 5:00 PM PST / 8:00 PM EST on Zoom! CLICK HERE TO REGISTER This is your chance to: - Learn about the TEMPO Phase 3 clinical trial of pitolisant, a potential treatment for […]
Sip, Savor, Support! Join Clint and Karla Hurdle on Saturday, March 22, 2025, to support PWSA | USA. Enjoy the 11th Annual Hot Stove Dinner at this outdoor event on the beautiful grounds of Bradenton Country Club, Bradenton, FL, or virtually from anywhere. REGISTER HERE! Event Schedule: 5:00 PM EST - 6:00 PM EST | […]
When: Saturday, April 5, 2025 | 6:00 PM Where: Historical Hall (608 Old Post Road, Bedford NY) CLICK HERE TO REGISTER AND BECOME AN EVENT SPONSOR Join us for the inaugural Zahra’s Night of Light at the Historic Hall in Bedford, NY! This community event brings us together to support children like Zahra, living with Prader-Willi Syndrome. […]
Date: Wednesday, April 16, 2025Time: 9:15 AM PT | 12:15 PM ETLocation: Virtual via ZOOM Free for anyone to attend REGISTER HERE The Prader-Willi syndrome (PWS) community has reached a historic milestone – VYKAT XR (formerly known as DCCR in clinical trials) is now FDA-approved as the first-ever treatment for hyperphagia in PWS. To help families, caregivers, and […]
CLICK HERE TO REGISTER When: Tuesday, April 22, 2025 | 9:00 PM ET / 6:00 PM PT PWS families and caregivers are invited to a virtual town hall focused on VYKAT XR, the first FDA-approved medication for treating hyperphagia in individuals with Prader-Willi syndrome (PWS) ages 4 and older. This informal, community-led town hall is […]
CLICK HERE TO REGISTER Join PWSA | USA, The Endocrine Society, and Medscape Education for this live symposium on Prader Willi syndrome (PWS) where experts will explore the huge burden that hyperphagia represents for patients with PWS, their families, and their caregivers. They will delve into the pathophysiology and complications of hyperphagia and look to […]
We are excited to introduce the United We Brunch initiative, a nationwide effort designed to bring people together to connect, share experiences, gain the resources, and support our community needs. United We Brunch is about fostering hope – one brunch, one state, and one family at a time – uniting communities and creating a ripple effect of awareness and […]
Throughout May, Help Shine a Light on Prader-Willi Syndrome Awareness Month! The month of May is an important time for our rare disease community because it's recognized as Prader-Willi Syndrome Awareness Month. While advocacy efforts, the fight for research advancements, and celebration of our loved ones is important 365 days a year, the 31 days […]
When: Saturday, May 3, 2025 | 9:00 AM Where: Greater Wilson Rotary Park (1901 Branch St NW, Wilson, NC 27893) CLICK HERE TO REGISTER! Early bird ticket pricing ends March 20th! Register to ATTEND or SPONSOR the NC Hope United 5K & Family Fun Run in support of individuals living with Prader-Willi Syndrome! Proceeds from this […]
CLICK HERE TO REGISTER When: Wednesday, May 14, 2025 | 9:00 AM PT / 12:00 PM ET Where: Virtual via Zoom Free for anyone to attend! About Ivailo Grigorov Ivailo Grigorov is a Financial Advisor and special needs parent to Lucca, who is 8 years old and has a diagnosis of Prader-Willi Syndrome. After 15 […]
Louisiana Families and Friends! There’s an Easy and Delicious Way to Support PWSA | USA this PWS Awareness Month. On two dates in May, Thursday, May 15, 2025 and Friday, May 30, 2025, several restaurants across Louisiana are generously donating a portion of their sales to PWSA | USA in honor of Prader-Willi Syndrome Awareness Month. […]
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.
