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.

2018 Worldwide LAM Awareness Month

June is Worldwide LAM Awareness Month (WWLAM). Lymphangioleiomyomatosis (LAM) is a rare, incurable lung disease. [...]

Traveling with LAM

I mention it often here – I have a fatal, incurable lung disease called lymphangioleiomyomatosis [...]


Working full-time with LAM

I found out about my LAM just one year after graduating from university with a [...]

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Being an athlete with LAM

It took crossing the finish line of my first marathon for me to consider myself [...]

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Exercising with LAM

A couple years after my LAM diagnosis, I decided to take an outdoors fitness bootcamp [...]

Being a Nana with LAM

On April 1, 2013, my whole life changed. I was diagnosed with LAM. I was [...]


Being a godparent with LAM

My name is Catrin. I’m 45 years old, married, and live in Germany close to the [...]

Being a working mom with LAM

In 2008, I was in my final weeks of graduate school at the University of [...]


Doing physical therapy with LAM

Hi my name is Bree and I live in the coastal town of Capel Sound [...]

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Worldwide LAM Awareness Month

June is Worldwide LAM Awareness Month (WWLAM)! Ten women contributed their stories for us to share [...]