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?
Start Here
The Latest News
-
Blog LAM Patient Research and Priorities Survey Provides Key Insights
-
Blog LAM Patients Advocate for Supplemental Oxygen Access Reform During Rare Across America
-
Blog CpG-ODN as novel LAM immunotherapy
-
Events Join The LAM Foundation on Giving Tuesday
-
Blog Advocating for Women in Rare Diseases: LAM Foundation’s Call to the FDA Innovation Hub
