Your Strength.
Our Support.
For more than 25 years, The LAM Foundation has provided hope and support to individuals facing this devastating rare disease. Our unwavering commitment is to empower our patient community and urgently drive research toward better treatments and a cure.
About Us
LAM
(Lymphangioleiomyomatosis)
LAM triggers the abnormal growth of smooth muscle cells, especially in the lungs, lymphatic system, and kidneys.
The disease strikes women almost exclusively and has no known cure.
Advances in research provide hope for a better quality of life and ultimately a cure.
Newly Diagnosed?
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The Latest News
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Blog LAM Patients Advocate for Supplemental Oxygen Access Reform During Rare Across America
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Blog Assessing Unsupervised Exercise in Interstitial Lung Disease
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Blog New Automated Method to Segment and Measure Lymphangioleiomyomatosis Lung Cysts in CT Images
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Blog I Am a LAM Patient and Oxygen Advocate. Here’s Why Congress Needs to Pass the SOAR Bill.
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Events Optimizing Nutrition in Lung Transplant: Step-by-Step Guide for Pre and Post Transplant Recipients
