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
Oct
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
Jun
WWLAM 2021: Susan
For Worldwide LAM Awareness Month (WWLAM) 2021, we’re sharing stories from women who were diagnosed [...]
May
WWLAM 2021: Sarah
For Worldwide LAM Awareness Month (WWLAM) 2021, we’re sharing stories from women who were diagnosed [...]
May
WWLAM 2021: Alex
For Worldwide LAM Awareness Month (WWLAM) 2021, we’re sharing stories from women who were diagnosed [...]
1 Comments
May
WWLAM 2021: Meagan
For Worldwide LAM Awareness Month (WWLAM) 2021, we’re sharing stories from women who were diagnosed [...]
1 Comments
May
The sound of life with LAM
I met Sina in 2016 in Berlin. She was the first woman with LAM I [...]
Feb
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 [...]
Jun
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
May