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Self Help Clearinghouse

This information is provided as a resource and does not constitute an endorsement for any group. It is the responsibility of the reader to decide whether a group is appropriate for his/her needs. For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site.

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.
The LAM Foundation
c/o Jill Raleigh
4015 Executive Park
Cincinnati, OH 45241
Voice: 513-777-6889
Fax: 513-777-4109
Verified: 9/2/2011

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