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Information and stories about living with LAM. Lymphangioleiomyomatosis (LAM) is a rare, chronic lung disease.
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 [...]
The first woman with LAM I made on this journey was Sina. I met her [...]
We got lucky with the timing of our trip to Tokyo. The last day we [...]
When we set out on this adventure, I posted a message about our trip on [...]
During our week in the wonderful city of Edinburgh, I had the pleasure of meeting [...]
One of the goals of this journey Justin and I are on is to meet [...]
Because I have LAM, my lungs don’t work as well as a healthy person’s so [...]