Tag Archives: LAM stories
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
How LAM impacts daily life
People who don’t have lymphangioleiomyomatosis (LAM) probably don’t understand what it’s like living with a [...]
Jun
Positive perspectives for women with LAM
Having lymphangioleiomyomatosis (LAM) is awful. Not only is the physical decline challenging, the psychological effects [...]
Jun
Advice for newly diagnosed women with LAM
I know first hand how scary it is to get a diagnosis of lymphangioleiomyomatosis (LAM). [...]
2 Comments
Jun
Being your own advocate
Being your own advocate and trusting your instincts is so important when you have a [...]
Jun
LAM community support
Being an active member of the lymphangioleiomyomatosis (LAM) community has really helped me cope with [...]
3 Comments
Jun