The LAM Foundation is the global leader in the fight against lymphangioleiomyomatosis (LAM). We are dedicated to finding safe and effective treatments, and ultimately a cure, for women living with LAM. Your gift is essential to making a difference in their lives.

All contributions directly support The LAM Foundation’s research, advocacy and patient education initiatives. The LAM Foundation is a registered 501(c)3 non-profit organization. All contributions are tax-deductible to the fullest extent of the law. If you have any questions about your gift, please call us at 513-777-6889 or email us at development@thelamfoundation.org.

Worldwide LAM Awareness Month

June has been designated Worldwide LAM Awareness Month (WWLAM) by the Worldwide LAM Patient Coalition. WWLAM brings together the global community in a collaborative effort to educate the world about the signs and symptoms of LAM, raise funds to support women living with LAM, and inspire researchers and clinicians to optimize therapies and find a cure for LAM.

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Give the Gift of Hope

"Hope came to me in the form of The LAM Foundation and its sisterhood of women. I’m thankful that the Foundation has encouraged donations that have led to life-improving treatments. I believe eventually the gifts of caring people will lead to a cure." - Meg, diagnosed in 2017

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Francis X. McCormack Career Development Award Fund

As part of Dr. McCormack's passion for leading, inspiring, and expanding promising LAM research, he has consistently encouraged young scientists and clinicians to study LAM. To acknowledge his investment in the future of LAM science, we named an annual LAM research award in his honor: The Francis X. McCormack Career Development Award.

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Donate Online

By making a donation today, your gift has an immediate impact on women living with LAM around the world. We are truly grateful for your generous support.

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