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WHO WE ARE

Connecting families, professionals, and researchers to build a better future for the PWSACO community.
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.

Our Board Members

JEFF & KARI PORTER

Board President & Member

GARY & LYNETTE HOSLER

Board President & Member

LORI HARRY

Board Member

MARK GREENBERG

Board Member

ROBIN FLEISCHMAN

Board Member

AMY PORTER

Board Member

ROBIN GRAY

Board Member

Get Connected

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