The LAM Foundation is a non-profit organization dedicated to supporting individuals affected by Lymphangioleiomyomatosis (LAM), a rare lung disease that primarily affects women. The foundation aims to raise awareness, provide education, and fund research to improve the understanding and treatment of LAM. In addition to research funding, the LAM Foundation offers resources for patients and families, including support groups and informational materials. They work closely with healthcare professionals to ensure that those impacted by LAM receive the best possible care and support throughout their journey.