Every leiomyosarcoma (LMS) diagnosis deserves to be understood individually. Every patient deserves access to knowledgeable specialists. And every patient deserves hope grounded in credible information and advances in research.
At the National Leiomyosarcoma Foundation (NLMSF), our commitment to you is to make the science understandable, the resources accessible, and the patient voice stronger — keeping patients and their families at the center of everything we do.
A new diagnosis of leiomyosarcoma can feel frightening and overwhelming. Patients and caregivers may be uncertain where to turn, what questions to ask, or how to navigate the journey ahead.
You do not have to face this journey alone.
Through our website, educational programs, resources, and direct support, NLMSF is committed to helping patients and their families and caregivers:
- Understand your diagnosis through clear, credible, patient-friendly information.
- Ask informed questions and have more meaningful conversations with their healthcare team.
- Find knowledgeable specialists and resources to help guide their care.
- Strengthen YOUR voice and advocate for themselves throughout their journey.
- Feel supported and empowered from diagnosis through treatment, survivorship, and beyond.
Our commitment is to you. Your voice matters. Your questions matter. And you are not alone.
Together, we can help patients and families navigate the challenges of leiomyosarcoma with greater knowledge, stronger advocacy, meaningful support, and hope.