Ann Arbor, MI Lymphangioleiomyomatosis. The LAM Foundation International...

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The LAM Foundation

International network. Founded 1995. Provides education for doctors, patients and support for women and their families who have LAM (lymphangioleiomyomatosis). LAM is a rare lung disease affecting only women, where smooth muscle cells grow throughout the lungs. A newsletter for general distribution and patient listserv, Personal Journeys, Lung Transplantation Booklet, advocacy program and newsletter solely for patients.
Write:
The LAM Foundation
4015 Executive Park, Suite 320
c/o Leslie Sullivan-Stacey
Cincinnati, OH 45241
Voice: 513-777-6889
Fax: 513-777-4109
Website: http://www.thelamfoundation.org
E-mail: info@thelamfoundation.org
Verified: 10/8/2008

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