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Lymphangioleiomyomatosis

Self Help Clearinghouse

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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. Newsletter for general distribution, patient listserv, 'Personal Journeys', advocacy program and newsletter solely for patients.

Write:

The LAM Foundation

c/o Jill Raleigh

4015 Executive Park

Cincinnati, OH 45241

Voice: 513-777-6889

Fax: 513-777-4109

Website: http://www.thelamfoundation.org

E-mail: info@thelamfoundation.org

Verified: 9/2/2011

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