Please select all the ways you would like to hear from Travel Breathe Repeat:
You can unsubscribe at any time by clicking the link in the footer of our emails. For information about our privacy practices, please visit our website.
We use Mailchimp as our marketing platform. By clicking below to subscribe, you acknowledge that your information will be transferred to Mailchimp for processing. Learn more about Mailchimp's privacy practices here.
Information and stories about living with LAM (lymphangioleiomyomatosis) based on Sarah’s personal experience with this rare, chronic lung disease.
The LAM community is small, with only a few thousand cases known worldwide. So it’s [...]
I was diagnosed with lymphangioleiomyomatosis (LAM) almost nine years ago. In that time, Justin and [...]
Medical students are taught to think of horses instead of zebras when they hear hoofbeats. [...]
June is Worldwide LAM Awareness Month (WWLAM). Lymphangioleiomyomatosis (LAM) is a rare, incurable lung disease. [...]
I mention it often here – I have a fatal, incurable lung disease called lymphangioleiomyomatosis [...]
I found out about my LAM just one year after graduating from university with a [...]
It took crossing the finish line of my first marathon for me to consider myself [...]
A couple years after my LAM diagnosis, I decided to take an outdoors fitness bootcamp [...]
On April 1, 2013, my whole life changed. I was diagnosed with LAM. I was [...]
My name is Catrin. I’m 45 years old, married, and live in Germany close to the [...]