The Lam Foundation, based in Sharonville, OH, has been providing hope and support to individuals facing the rare disease lymphangioleiomyomatosis (LAM) for over 25 years. Their unwavering commitment is to empower the patient community and drive research towards better treatments and ultimately a cure.
LAM triggers abnormal growth of smooth muscle cells in the lungs, lymphatic system, and kidneys, predominantly affecting women with no known cure. Through advances in research, the foundation aims to improve quality of life for those with LAM and work towards finding a cure for this devastating disease.
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