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.
Thriving with LAM: Steph
Steph is sharing her story of hope and resilience as part of our “Thriving with [...]
May
Thriving with LAM: Shea
Shea is sharing her story of hope and resilience as part of our “Thriving with [...]
May
Thriving with LAM: Najah
Najah is sharing her story of hope and resilience as part of our “Thriving with [...]
7 Comments
May
Thriving with LAM: Dina
Dina is sharing her story of hope and resilience as part of our “Thriving with [...]
1 Comments
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
How travel has helped me cope with chronic illness
I was diagnosed with lymphangioleiomyomatosis (LAM) almost nine years ago. In that time, Justin and [...]
5 Comments
Jun
Showing my stripes for Rare Disease Day
Medical students are taught to think of horses instead of zebras when they hear hoofbeats. [...]
1 Comments
Feb