Living with LAM

Read personal stories and advice about living with lymphangioleiomyomatosis (LAM),based on Sarah’s and others’ personal experiences with this rare, chronic lung disease.


Patient Stories

Hear from people living with LAM around the world.

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Sarah’s Advice

Read Sarah’s story, tips, and musings about living with LAM.

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Read about the incredible times Sarah and Justin met people in the LAM community.

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Worldwide LAM Awareness Month

Peruse the WWLAM Archives from throughout the years.

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Share Your Story

Are you living with LAM and interested in sharing your story?

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