Tag Archives: LAM stories

Thriving with LAM: Dina

Dina is sharing her story of hope and resilience as part of our “Thriving with [...]

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Thriving with LAM: Meg

Meg is sharing her story of hope and resilience as part of our “Thriving with [...]

Thriving with LAM: Maria

Maria is sharing her story of hope and resilience as part of our “Thriving with [...]

Thriving with LAM: Sally

Sally is sharing her story of hope and resilience as part of our “Thriving with [...]

Taking control of life and LAM: Stephanie’s story living with a rare disease

The LAM community is small, with only a few thousand cases known worldwide. So it’s [...]

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2018 Worldwide LAM Awareness Month

June is Worldwide LAM Awareness Month (WWLAM). Lymphangioleiomyomatosis (LAM) is a rare, incurable lung disease. [...]

Traveling with LAM

I mention it often here – I have a fatal, incurable lung disease called lymphangioleiomyomatosis [...]

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Working full-time with LAM

I found out about my LAM just one year after graduating from university with a [...]

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Being an athlete with LAM

It took crossing the finish line of my first marathon for me to consider myself [...]

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Exercising with LAM

A couple years after my LAM diagnosis, I decided to take an outdoors fitness bootcamp [...]