by Fran Howard, in RT Magazine

The LAM Foundation is a breath of hope for those with a rare lung condition

Nearly 20 years ago when 31 year-old Susan Jardine of Mill Valley, Calif. was diagnosed with lymphangioleiomyomatosis (LAM), only a handful of physicians in the United States had even heard of the disease. She was told that LAM was a rare and fatal lung disease with no cure.