The LAM Foundation
EIN: 31-1438001 · Cincinnati, OH
Our Story
In the early 1990s, Sue Byrnes established The LAM Foundation after her daughter Andrea was diagnosed with lymphangioleiomyomatosis (LAM). With limited information available, Sue's determination to find answers led to the creation of a global leader in LAM research and advocacy.
Impact
Since its inception, The LAM Foundation has raised nearly $34 million, with over $18 million allocated to groundbreaking research, resulting in the first FDA-approved treatment for LAM.
Why Donate?
Your contributions directly support vital research, advocacy, and education initiatives, significantly impacting the lives of women living with LAM and propelling the search for effective treatments and a cure.
Get Involved
Join the fight against LAM by donating today. Your support can help change lives and drive research forward. Whether through cryptocurrency or cash, every contribution counts!
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