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Information and stories about living with LAM (lymphangioleiomyomatosis) based on Sarah’s personal experience with this rare, chronic lung disease.
In 2008, I was in my final weeks of graduate school at the University of [...]
Hi my name is Bree and I live in the coastal town of Capel Sound [...]
June is Worldwide LAM Awareness Month (WWLAM)! Ten women contributed their stories for us to share [...]
People who don’t have lymphangioleiomyomatosis (LAM) probably don’t understand what it’s like living with a [...]
Having lymphangioleiomyomatosis (LAM) is awful. Not only is the physical decline challenging, the psychological effects [...]
I know first hand how scary it is to get a diagnosis of lymphangioleiomyomatosis (LAM). [...]
Being your own advocate and trusting your instincts is so important when you have a [...]
Being an active member of the lymphangioleiomyomatosis (LAM) community has really helped me cope with [...]
According to the LAM Foundation, the symptoms of lymphangioleiomyomatosis (LAM) can include: Shortness of breath [...]
Lymphangioleiomyomatosis (LAM) is a degenerative lung disease. As the disease progresses, one’s lung function decreases. [...]