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. [...]
Jun
Traveling with LAM
I mention it often here – I have a fatal, incurable lung disease called lymphangioleiomyomatosis [...]
11 Comments
Jun
Working full-time with LAM
I found out about my LAM just one year after graduating from university with a [...]
1 Comment
Jun
Being an athlete with LAM
It took crossing the finish line of my first marathon for me to consider myself [...]
1 Comment
Jun
Exercising with LAM
A couple years after my LAM diagnosis, I decided to take an outdoors fitness bootcamp [...]
Jun
Being a Nana with LAM
On April 1, 2013, my whole life changed. I was diagnosed with LAM. I was [...]
5 Comments
Jun
Being a godparent with LAM
My name is Catrin. I’m 45 years old, married, and live in Germany close to the [...]
Jun
Being a working mom with LAM
In 2008, I was in my final weeks of graduate school at the University of [...]
3 Comments
Jun
Doing physical therapy with LAM
Hi my name is Bree and I live in the coastal town of Capel Sound [...]
1 Comment
Jun
Worldwide LAM Awareness Month
June is Worldwide LAM Awareness Month (WWLAM)! Ten women contributed their stories for us to share [...]
Jun