Patient Quality of Life Awards
The LAM Foundation's Patient Quality of Life Awards fund research to improve daily living and patient-centered outcomes for people with lymphangioleiomyomatosis.
Funder: The LAM Foundation
Due Dates: June 15, 2026 (LOI) | September 15, 2026 (Full proposal, invited only)
Funding Amounts: Up to $25,000 for a one-year project period; direct costs only.
Summary: Supports research projects that deliver meaningful improvements in the daily lives of individuals with lymphangioleiomyomatosis (LAM), with an emphasis on patient-centered outcomes.
Description
The Patient Quality of Life Awards, part of The LAM Foundation Grant Program, fund research that aims to significantly improve the quality of life for individuals living with lymphangioleiomyomatosis (LAM). The program encourages innovative, rigorous projects that address unmet needs in LAM patient care, support, and daily living. Proposals may use qualitative or quantitative approaches but must include the patient voice and clearly articulate both immediate and anticipated real-world outcomes. The ultimate goal is to translate research findings into tangible, positive impacts for people with LAM.
