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Information and stories about living with LAM (lymphangioleiomyomatosis) based on Sarah’s personal experience with this rare, chronic lung disease.
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. [...]
Travel Breathe Repeat is a travel blog. One of the people traveling just happens to have [...]
While in Australia, I was lucky to meet women with LAM and other members of the [...]
Last year when I started talking to the LAM Foundation about this trip and mentioned [...]