The LAM Foundation

Organization URL(s)

Other Contact Information

4015 Executive Park Drive, Suite 320
Cincinnati, OH 45241-1335
1-877-2873-526 (Voice - Toll-free)
513-777-6889 (Voice)
513-777-4109 (FAX)


The LAM Foundation provides support, education, and hope to women with Lymphangioleiomyomatosis (LAM), a progressive, debilitating lung disease. Our goals are to organize, marshal the forces of the scientific community, raise LAM from obscurity, and conquer it in a decade. The Foundation holds an annual research conference in Cincinnati for physicians, scientists and patients. Research pilot projects are funded at $10,000-$25,000 and three-year fellowships are funded from $35,000-$50,000 each year.

Print Resources

The LAM Foundation was founded in August, 1995 by Fran and Sue Byrnes after their 22 year old daughter was diagnosed with LAM.

Review Date

Thursday, Nov 04, 2010