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Information and stories about living with LAM (lymphangioleiomyomatosis) based on Sarah’s personal experience with this rare, chronic lung disease.
The past year, I learned the power of gratitude. It started as a technique to [...]
I was diagnosed with LAM 11 years ago. It was a tough day and an [...]
For Worldwide LAM Awareness Month (WWLAM) 2021, we’re sharing stories from women who were diagnosed [...]
I met Sina in 2016 in Berlin. She was the first woman with LAM I [...]
I’m excited to share my participation in the new book Breathe, Just Breathe. Like our [...]
June has always been a time to reflect on what having the rare lung disease, [...]