Tag Archives: LAM stories
Thriving with LAM: Dina
Dina is sharing her story of hope and resilience as part of our “Thriving with [...]
1 Comment
May
Thriving with LAM: Meg
Meg is sharing her story of hope and resilience as part of our “Thriving with [...]
May
Thriving with LAM: Maria
Maria is sharing her story of hope and resilience as part of our “Thriving with [...]
May
Thriving with LAM: Sally
Sally is sharing her story of hope and resilience as part of our “Thriving with [...]
May
Taking control of life and LAM: Stephanie’s story living with a rare disease
The LAM community is small, with only a few thousand cases known worldwide. So it’s [...]
2 Comments
Feb
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