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.

Gratitude and chronic illness

This year, I learned the power of gratitude. It started as a technique to help [...]

5 Comments

11 things I wish I knew 11 years ago

I was diagnosed with LAM 11 years ago. It was a tough day and an [...]

7 Comments

WWLAM 2021: Susan

For Worldwide LAM Awareness Month (WWLAM) 2021, we’re sharing stories from women who were diagnosed [...]

WWLAM 2021: Sarah

For Worldwide LAM Awareness Month (WWLAM) 2021, we’re sharing stories from women who were diagnosed [...]

WWLAM 2021: Alex

For Worldwide LAM Awareness Month (WWLAM) 2021, we’re sharing stories from women who were diagnosed [...]

1 Comments

WWLAM 2021: Meagan

For Worldwide LAM Awareness Month (WWLAM) 2021, we’re sharing stories from women who were diagnosed [...]

1 Comments

The sound of life with LAM

I met Sina in 2016 in Berlin. She was the first woman with LAM I [...]

New book of portraits and profiles of women with LAM

I’m excited to share my participation in the new book Breathe, Just Breathe. Like our [...]

Thriving with LAM: stories of hope and resilience

June has always been a time to reflect on what having the rare lung disease, [...]

1 Comments