Category Archives: Living with LAM
Information and stories about living with LAM (lymphangioleiomyomatosis) based on Sarah’s personal experience with this rare, chronic lung disease.
How LAM impacts daily life
People who don’t have lymphangioleiomyomatosis (LAM) probably don’t understand what it’s like living with a [...]
Jun
Positive perspectives for women with LAM
Having lymphangioleiomyomatosis (LAM) is awful. Not only is the physical decline challenging, the psychological effects [...]
Jun
Advice for newly diagnosed women with LAM
I know first hand how scary it is to get a diagnosis of lymphangioleiomyomatosis (LAM). [...]
2 Comments
Jun
Being your own advocate
Being your own advocate and trusting your instincts is so important when you have a [...]
Jun
LAM community support
Being an active member of the lymphangioleiomyomatosis (LAM) community has really helped me cope with [...]
3 Comments
Jun
Symptoms of LAM
According to the LAM Foundation, the symptoms of lymphangioleiomyomatosis (LAM) can include: Shortness of breath [...]
Jun
Healthy living with LAM
Lymphangioleiomyomatosis (LAM) is a degenerative lung disease. As the disease progresses, one’s lung function decreases. [...]
Jun
Tips for traveling with LAM
Travel Breathe Repeat is a travel blog. One of the people traveling just happens to have [...]
3 Comments
Jun
LAM meet-ups in Australia
While in Australia, I was lucky to meet women with LAM and other members of the [...]
2 Comments
Apr
LAM meet-up in Auckland
Last year when I started talking to the LAM Foundation about this trip and mentioned [...]
3 Comments
Mar