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Featured Article


Finding Hope Through LAM Community Engagement

Posted on May 14, 2021   |   

I was diagnosed with LAM and probable Tuberous Sclerosis Complex (TSC) in 2019 at 26 years old, when I was working three jobs and attending graduate school in Colorado. As an active twenty-something still trying to figure out my life, the stress of understanding what this diagnosis meant for my future weighed heavily on me.

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Topics: Community Engagement diagnosis        Categories: Patient Profiles

Recent Articles

Author: A. Bloomer

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Genetics Research into LAM Leads to a New Discovery

Posted on July 01, 2019   |   
Author: A. Bloomer

Genetic research sponsored by The LAM Foundation has led to a new discovery!
We need your help to learn more.

What can saliva samples teach us about LAM? It took a global network of patients, researchers, and donors like you to find out. Everything began with one common connection—The LAM Foundation. We are the global leader in the fight against lymphangioleiomyomatosis (LAM). By donating to The LAM Foundation, your gifts help move us closer to finding safe,

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Categories: News
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