The LAM Foundation is a global leader in the fight against lymphangioleiomyomatosis (LAM), a rare and progressive lung disease primarily affecting women. Founded in 1995, the organization is dedicated to funding promising research, advocating for safe and effective treatments, and ultimately finding a cure for LAM.
Through its support and education programs, The LAM Foundation provides information, resources, and a worldwide network of hope and support for women with LAM and their families. The organization also engages doctors and scientists to further understand the disease, raises funds for continued research, and has played a significant role in the approval of the first effective treatment for LAM. With a focus on targeted scientific research and improved patient care, The LAM Foundation aims to drive the completion of clinical trials, develop biomarkers for diagnosis and disease progression, and ultimately find a cure for LAM.
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