The Montana Medicaid Drug Use Review Board will be meeting virtually from 1 PM – 5 PM MT on Wednesday, Sept. 17, 2025.
Here’s how you can help:
The Medicaid Drug Use Review Board needs to hear directly from you – the parents, caregivers, and family members who understand the real-life impact of hyperphagia (excessive hunger) in PWS. One of the medications under review is Vykat XR, the first-ever hyperphagia treatment specifically for individuals living with PWS that was approved by the FDA in March 2025.
We’re asking families to submit written testimony to help decision-makers understand why access to this treatment is so urgently needed.
Submission Details:
Max TWO Pages
May include photo
Medicare/Medicaid/Medicaid Waiver recipients are favored
Meeting Details:
- When: Wednesday, September 17th
- Time: 1:00 – 5:00P MT (Virtual Only)
- Advanced Registration Required: https://events.teams.microsoft.com/event/00ce34a5-f2d8-4b55-ad85-c09a5acf02dd@1f053f7a-e47d-43fd-9182-8507c9ff10c7
Meeting Agenda can be found at: September 17, 2025
Policies and Procedures for providing comments: https://dphhs.mt.gov/boardscouncils/medicaiddur
Should you decide to provide written or oral testimony, please be aware of the need to comply with all necessary disclosure requirements regarding your employer, as well as any business relationships you may have (or had) with Soleno Therapeutics, Inc. and/or other companies that may have an interest in this meeting.
If you are interested in providing oral testimony, please complete the Public Testimony Form and submit it by Noon the day prior to the meeting. Individual comment will be limited to a maximum of 3 minutes per person and is subject to further limitations depending on the number of speakers (15 minutes divided by total speakers).
If you would like to provide written testimony, please refer to the requirements for submission within the MT Medicaid DURB webpage. To allow the board adequate time to review and research. Please email written comments and/or clinical information, with a statement indicating that it is public comment, to PDL@mt.gov at least 7 days prior to the meeting. Please limit information to 2 pages.
Writing Guide:
- My name is:
- I live in:
- My child living with PWS is ___ old and receives Medicaid in the state of MT.
- Thank the members of the committee for the work they do.
- How do the unmet needs of PWS affect your family?
- If your son/daughter IS taking vykat XR, explain how access to the drug has changed your lives?
- If your son/daughter IS NOT taking vykat XR, how will having access to an approved drug to treat hyperphagia in PWS change their lives and what their future looks like?
- What is your hope for the approval of drugs to treat hyperphagia in PWS.
Review:
If you’d like help drafting your story or want someone to review it with you, PWSA | USA is here to support you. Reach out to a fellow parent or contact us directly (info@pwsausa.org or 941.312.0400).
Remember, the experts will cover the science; your testimony will touch the hearts of the decision-makers. Bring them to tears with the reality of our challenges and the promise of what could be. This is where the power is.
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.