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Who We Are 2018-03-28T05:34:26+00:00

Our Mission

The Prader-Willi Syndrome Association of Colorado (PWSACO) is committed to improving the quality of life and the life expectancy of those affected by Prader-Willi Syndrome (PWS), by providing emotional support, social services or care for individuals with PWS. We will work to increase awareness of PWS within society and the medical community, and will actively support research directed at improving diagnosis, quality of life, and most importantly, finding a cure.

PWSACO provides the following services

  • Direct assistance to our families through grants to cover costs of medical treatments, travel to conferences, social work, etc.
  • Support for the PWS multi-disciplinary clinic at the Children’s Hospital of Colorado
  • Funding of research projects through the Foundation for Prader-Willi Research (www.fpwr.org)
  • Seeking a long-term care solution for our PWS adult population in Colorado
  • Advocacy on PWS and disability issues with state, federal and local governments, including school systems

Our Board Members

LYNETTE HOSLERBoard President
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JEFF PORTERBoard President
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CHARLOTTE PETERSONBoard Member
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LORI HARRYBoard Member
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CRYSTAL REDNERBoard Member
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GARY HOSLERBoard Member
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ROBIN FLEISCHMANBoard Member
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MARK GREENBERGBoard Member
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KARI PORTERBoard Member
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Get Connected

PWSACO is a volunteer-run, non-profit organization devoted to supporting individuals with Prader-Willi syndrome and their families.

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