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Family Support Webinar: Psychosis in PWS – Early Signs, Diagnosis, and Treatment
Join PWSA | USA and Elizabeth Roof, MA, HSP, on Tuesday, March 26th to learn more about Psychosis in PWS: Early Signs, Diagnosis, and Treatment. The webinar will begin at 5pm PST/ 8pm EST. Elizabeth Roof is a Senior Research Associate at Vanderbilt University Department of Psychology and has been licensed as a Health Service Provider in Tennessee since 1994. She currently directs several research programs with children and adults with Prader-Willi syndrome alongside Elisabeth Dykens. For over 30 years, Elizabeth has followed longitudinally over 400 children, teens, and adults with PWS in research studies. She has a wealth of knowledge and experience with PWS and has valuable insights to offer in the realm of psychosis in PWS. Register for the webinar below.
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.