Within the LMS community, everyone has a unique experience and sharing our narratives empowers the storyteller and all those who listen. Within the sarcoma community, those individual voices unite to serve as a core transformative component for the care paradigm with an emphasis on patient experience. This network can generate recommendations for changes to the standard of care—from initial diagnosis to end of treatment—that will create a legacy for those patients and caregivers who come after us.
National LeioMyoSarcoma Foundation
helping to empower and educate about leiomyosarcoma a rare smooth tissue cancer