Abbott Philson is 41 years old and lives with Prader-Willi syndrome. He lives in Maine and has been a board member for PWSA | USA for 25 years. In an effort to learn more about our adults with PWS, and to shine a light on their lives and experiences, we asked our Advisory Board members...
Aardvark Therapeutics recently launched HERO, a global Phase 3 clinical trial investigating ARD-101, an innovative, orally administered treatment designed to help reduce hyperphagia (excessive hunger) and food-seeking behaviors in individuals with Prader-Willi syndrome (PWS). This randomized, double-blind, placebo-controlled trial is an important step toward identifying a potential new treatment option for the PWS community, and...
submitted by Sarah Kasaby, mom to Khaled (living with PWS)
submitted by Caitlin Heckman, mom to Ada (1, living with PWS) We received Ada’s PWS diagnosis when she was one month old, and, like everyone in this community, our world was turned upside down. This condition we previously had no idea existed became the center of our attention. The NICU doctor who gave us her...
Question: Female, 42 years old, UPD subtype My question is about treatment for osteoporosis. My sister, to my knowledge, has never had any hormone replacement. She is obese, BMI 38, and the only abnormal lab done by her gynecologist was testosterone, which was “below the technical range of the assay.” Her vitamin D levels are...
We have an exciting opportunity to livestream a session at our 2025 International PWS United in Hope Conference! If you haven’t listened to PWS United yet, we have quite a collection of PWS-related episodes, from research to advocacy, family support, and more. We will be recording some of the upcoming conference sessions to share with...
Kate Kane is 43 years old and lives with Prader-Willi syndrome. She is legally a resident in the state of Maryland but resides in a home in Wisconsin for people with PWS. Kate has been a board member for PWSA | USA for over 15 years. In an effort to learn more about our adults...
Question: Female, 22 years old, unknown subtype Hello, my daughter has severe rectal picking issues to the point she is anemic. Got it under control in June 2023. Latest labs show anemia Ferritin at 6 Iron total at 13 hemoglobin at 11.2…doc said increase iron supplement to 325mg. My concern is it’s a new doc...
James Towle is 39 years old and lives with Prader-Willi syndrome. He resides in Massachusetts and is “proud and honored to have been given the opportunity to serve on the board this past January 2025.” In an effort to learn more about our adults with PWS, and to shine a light on their lives and...
Question: Male, 8 months old, unknown subtype We want to give hCG injections to our son, not just to avoid the surgery but for future benefits as well. His endocrinologist and urologist refused to give hCG, even after requesting so many times. I’m from the UK, and the NHS (National Health Service) have stopped giving...
We are deeply saddened to share the news of the passing of Jim Gardner, a beloved and instrumental figure in the history of PWSA | USA. Jim’s unwavering dedication and tireless advocacy laid the foundation for much of the work we continue today. As one of the organization’s earliest champions, Jim helped shape PWSA |...
Aardvark Therapeutics recently launched HERO, a global Phase 3 randomized, double-blind, placebo-controlled clinical trial of ARD-101. ARD-101 is a novel, orally administered investigational therapy being studied to see if it can reduce excessive hunger and food-seeking behaviors in individuals with PWS. About the HERO Trial As part of the HERO study, participants will be randomly...
Trevor Ryan is 35 years old and lives with Prader-Willi syndrome. He resides in Arizona and has been a board member for 10 years. In an effort to learn more about our adults with PWS, and to shine a light on their lives and experiences, we asked our Advisory Board members some questions. Below are...
Conor Heybach is 44 years old and lives with Prader-Willi syndrome. He resides in Chicago and has been on the Adults with PWS Advisory Board since 1996. In an effort to learn more about our adults with PWS, and to shine a light on their lives and experiences, we asked our Advisory Board members some...
PWS Mom Jamie Caldwell, has found a unique way to celebrate her daughter, Lydia (3, living with PWS) and PWS Awareness Month. “We started working with this project after Kristina (Rieger), owner/founder of Dalya’s Dreamers, had posted in our local special needs mom group seeking models of her dresses. As a mother with a daughter...
Question: Female, 7 years old, Unknown deletion Does the identification of PWS by genetic testing PWS give conclusive results? In other words, your child either has or doesn’t have PWS? Does a child with PWS gain weight event if her caloric intake is restricted? Would a “less than normal” caloric intake still result in weight...
Shawn Cooper is 51 years old and lives with Prader-Willi syndrome. She resides in Georgia and has been on the Adults with PWS Advisory Board since it was first developed. In an effort to learn more about our adults with PWS, and to shine a light on their lives and experiences, we asked our Advisory...
The United in Hope 2025 PWS Conference schedule is live! To help us plan effectively, please let us know which sessions you’re most interested in attending. This isn’t an RSVP, just a quick way for us to gauge excitement and prepare accordingly. It only takes about 2 minutes. Please choose one session you’re most interested...
submitted by Dorothea Lantz, PWSA | USA’s Director of Community Engagement PWSA | USA Advocacy Community Update – Capitol Hill Recap (May 5–8, 2025) From May 5th–8th, six of our PWSA | USA Advocacy Ambassadors joined forces with the Council of Parent Attorneys and Advocates (COPAA) and key partners from the rare disease industry to...
Dini Rao, mom to Ayoni (8, living with PWS) hosted a very successful United We Brunch fundraiser for PWS Awareness Month. Desi Tea for Prader-Willi was on May 4th at the Rao home in Maryland. Neighbors, community members, and local PWS families gathered together for samosas, pakoras, chai, PWS awareness, and community. “When we first...
Question: Male, 18 years old, UPD subtype My son struggles with psychosis/schizophrenia for 1.5 yrs. None of the antipsychotics applied reduced the symptoms. He is in a miserable situation. The doctors want to use Clozapine as last resource. Is this a drug used frequently in people with PWS and psychosis? Do you have any suggestions...
Pennsylvania Families and Friends! There’s an Easy and Delicious Way to Support PWSA | USA on May 15 – PWS Awareness Day On Thursday, May 15, 2025, several restaurants across Pennsylvania are generously donating a portion of their sales to PWSA | USA in honor of Prader-Willi Syndrome Awareness Day. Whether you dine in, take out, or order online,...
submitted by Lisa Graziano, proud mom to Cameron (26, living with PWS) Cameron Graziano, age 26 with PWS deletion subtype, earned his Black Belt in Tae Kwon Do when he was 17 years old. His passion for Karate started at age 9 when his ability to balance on one foot did not exceed a count...
Victor Penta is 31 years old and lives with Prader-Willi syndrome. He resides in Arizona and has been on the Adults with PWS Advisory Board since 2019. In an effort to learn more about our adults with PWS, and to shine a light on their lives and experiences, we asked our Advisory Board members some...
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.
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
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.
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.
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.
