Author Archives: Sarah
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
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
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
Visiting Keukenhof gardens: tips for 2020
Are you a lover of tulips, flowers, bright colors, beautifully manicured gardens, and/or Instagrammable locations? [...]
32 Comments
Jan
Reflecting on milestones
June 17 is a pretty big day. Eight years ago today, I learned a very [...]
1 Comments
Jun
Traveling with LAM
I mention it often here – I have a fatal, incurable lung disease called lymphangioleiomyomatosis [...]
11 Comments
Jun
But it’s worth it
Travel has helped me cope with having a debilitating lung disease. It’s taken me outside [...]
16 Comments
Jan