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PWANY 30th Annual Conference

“Advocating for Advancement”
30th Annual Conference – May 20th & 21st in Binghamton, NY
Please join us as we “Advocate for Advancement” for the Prader-Willi Syndrome Community. We will have some of the top doctors and experts in the field on hand to present on current topics and answer your questions.
Presenters include:
- Dr. Moris Angulo: Nationally recognized specialist in Prader-Willi Syndrome with the largest number of patients in the US.
- Katherine Carpenter, ESQ: Wilcenski and Pleat attorney practicing in the areas of special needs planning, trust and estate administration and long-term care planning.
- Patrice Carroll: Latham Centers’ world-renowned Prader-Willi Syndrome specialist. She works with Latham Centers’ residents with PWS, their families and consultants.
- Sally Coletti: Founder of CNY Autism Society of America (CNYASA) & creator of Advocates for Autism, LLC
- Brittni Kliment: Latham Center’s Director of Program Marketing and Admissions
- Katrina Kozak: Latham Center’s Director of National Outreach
- Dr. Jorge Mejia Corletto: Pediatric Endocrinologist at Winthrop Hospital
- Barbara J. (BJ) Goff, Ed.D: Professor of Special Education at Westfield State University.
- Rachel Johnson: PWANY Executive Director, PWS Mom, Integrative Nutrition Coach & MSEd
- Dorothea Lantz: PWSA USA Community Engagement Specialist and PWS Parent
- Amy McDougall PWANY Board Vice President, School Psychologist and PWS Parent
- Maria Picone: Founder and CEO of TREND Community and PWS Parent
- Reva Reid: Occupational Therapist and Cortical Visual Impairment Therapist
- Anne Seepersaud: LifePlan CCO Regional VP, Care Management, Southern Tier and Capital
- Dr. Deepan Singh: Child, Adolescent and Adult Psychiatrist
- Cindy Szapacs: M.ED BCBA and PWS Parent
- Dr. VanBosse: Board certified by the American Board of Orthopedic Surgery. Adjunct Professor of Orthopedic Surgery at Thomas Jefferson University
- Stacy Ward: PWSA USA Director of Family Support and PWANY’s Provider Advisor

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.
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 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.
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.
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.