The Foundation embraces women with LAM and their families, provides support and education, engages doctors and scientists, and raises funds for the study of LAM. With research as its central mission, the Foundation has elevated LAM from the ranks of rare and forgotten diseases to the forefront of pulmonary medicine. The LAM Foundation funded the first LAM research that resulted in the fundamental understanding of the genetic cause of LAM and the first-ever LAM treatment trial.The LAM Foundation urgently seeks an effective treatment, and ultimately a cure, for lymphangioleiomyomatosis (LAM) through advocacy and the funding of promising research. We are dedicated to serving the scientific, medical and patient communities by offering information, resources and a worldwide network of hope and support.
Website: The LAM Foundation