Life Fest is a unique event where patients and caregivers come together for a weekend to interact with each other and the medical and scientific communities that serve them.
Faced with a rare form of cancer, liposarcoma patients have a great need for information about this disease, particularly as the science evolves and our understanding reveals a complex set of subtypes of liposarcoma, each responding differently to available treatments. Each year brings a wealth of new information, and patients are eager to learn about the latest treatments.
Life Fest workshops provide patients and caregivers with emerging medical information. Participants leave with a stronger understanding of the disease, available treatments, and how to manage side effects. In addition to our traditional educational workshops, Life Fest 2026 will feature scientific presentations highlighting the newest research and the latest treatments.
The Liposarcoma Support Network emerged in recognition of the tremendous need for support in the liposarcoma community. Life Fest 2026 will provide liposarcoma patients and caregivers the opportunity to gather for the very first time. Coming together with fellow patients from around the world is a meaningful and powerful experience.