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The LAM Foundation provides support, education, and hope to women with Lymphangioleiomyomatosis (LAM), a progressive, debilitating lung disease. Our goals are to organize, marshal the forces of the scientific community, raise LAM from obscurity, and conquer it in a decade.
The LAM Foundation serves women with LAM, or lymphangioleiomyomatosis, a progressive and frequently fatal lung disease that affects only women, usually in the prime of their lives. The Foundation provides support, education and the hope of a cure through scientific research to women with LAM around the world.
- Sally Lamb
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