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Information about what it’s like living with the rare, chronic lung disease, lymphangioleiomyomatosis (LAM).
The LAM community is small, with only a few thousand cases known worldwide. So it’s [...]
I was diagnosed with lymphangioleiomyomatosis (LAM) almost nine years ago. In that time, Justin and [...]
Medical students are taught to think of horses instead of zebras when they hear hoofbeats. [...]
June is Worldwide LAM Awareness Month (WWLAM). Lymphangioleiomyomatosis (LAM) is a rare, incurable lung disease. [...]
I mention it often here – I have a fatal, incurable lung disease called lymphangioleiomyomatosis [...]
I found out about my LAM just one year after graduating from university with a [...]
It took crossing the finish line of my first marathon for me to consider myself [...]
A couple years after my LAM diagnosis, I decided to take an outdoors fitness bootcamp [...]
On April 1, 2013, my whole life changed. I was diagnosed with LAM. I was [...]
My name is Catrin. I’m 45 years old, married, and live in Germany close to the [...]