Video Library

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Try as she might, Dawn Robinson couldn’t figure out what was wrong with her body. For eight years, she had consulted a wide range of specialists about numerous nagging health issues. Trouble breathing. Chest pain. Fatigue. It wasn’t until her lung collapsed in February 2020, that a resulting biopsy determined the cause: lymphangioleiomyomatosis (LAM).

Watch this video to hear Dawn's story and learn what The LAM Foundation means to her.

To make a donation The LAM Foundation visit, https://give.thelamfoundation.org/give/457347/#!/donation/checkout

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Thespena wants a cure for Lymphangioleiomyomatosis (LAM). Listen to her story to hear why supporting LAM research is important.

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DONATE TODAY: https://give.thelamfoundation.org/give/447817/#!/donation/checkout

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Please join us for the Day of Giving on Thursday, September 9, 2021. This day is an opportunity for the entire LAM community to come together on one day in a collective effort to Fund A Cure for LAM. Learn more: https://give.thelamfoundation.org/day-of-giving-2021

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"It takes all of us, and together, we can make it happen." - Sharlene Dunn

Please join us for the Day of Giving on Thursday, September 9, 2021. This day is an opportunity for the entire LAM community to come together on one day in a collective effort to Fund A Cure for LAM. Learn more: https://give.thelamfoundation.org/day-of-giving-2021

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The LAM Foundation urgently seeks safe and effective treatments, and ultimately a cure, for lymphangioleiomyomatosis (LAM) through advocacy and the funding of promising research. We are dedicated to serving the scientific, medical, and patient communities by offering information, resources, and a worldwide network of hope and support.

Founded in 1995, The LAM Foundation is the global leader in the fight against lymphangioleiomyomatosis (LAM).

LAM is a rare and progressive lung disease that primarily affects women and has no known cure. Headquartered in Cincinnati, Ohio, The LAM Foundation provides support and education for women with LAM and their families, engages doctors and scientists to continue to learn more about the disease, and raises funds for continued research. In May 2015, the FDA approved Rapamune as the first effective treatment for LAM, based on research and patient engagement supported by The LAM Foundation.

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