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
Rosie the Riveter wearing a LAM Foundation pin

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.

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