Your Strength.
Our Support.
For 30 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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Events LAMposium in Your Living Room
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Events Region 19: Northern California & Northern Nevada Educational Event
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Blog A Promising Breakthrough in Lung Testing for LAM Patients: introducing Oscillometry
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Blog LAMposium: What to Know Before you go
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Blog Pearls of Travel: A Special Way to Support LAM Research—and celebrate with a Cruise!
