Who Are We? Delving into the Rich History of Our Foundation
Tracing the Origins of the Foundation:
In 1997, a pioneering group of patients, caregivers, and families informally united to offer mutual support. By 2001, this collective became the officially named National Leiomyosarcoma Foundation, attaining its 501c3 status. Since 2002, the NLMSF has actively funded research. Today, we are proud to be distinguished as a 100% trusted organization by Charity Navigator, hold a Guide Star Gold designation, and are consistently recognized as a ‘Top Rated Charity’ by Great Nonprofits.”
Our Foundation's Board Members: A comprehensive showcase featuring photographs, names, and a designation as an LMS Survivor, Caregiver, or Friend of the Foundation, along with their respective locations across states or countries
Board Members
Achee, Annie - Colorado
Achee, Mitch - Colorado
Aguilar, Alex
Bain, Kathleen - Colorado
Forgess, Lynne - Philadelphia
Hancock, Chris - Washington
Lee, Greg - Canada
Sebaney, Jacque, - Texa,
Stoddard, Marlana- Oregon
Williams, Chandalyn
NLMSF Community Ambassadors
Corids, Charlee
Mathews, Jim
Noh, Denny
Our Foundation's Medical Advisory Committee for our 'Connect with a Clinician' Program: Featuring the names, titles, and sarcoma center locations, including both the city and state.