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Featured Article

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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: Dakota Campbell

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2018 Advances in LAM

Posted on December 21, 2018   |   

With your support, The LAM Foundation continues to thrive as a source of hope for individuals affected by LAM. We have again accelerated research and improved patient care, with each day moving us closer to a cure. Learn more about a few of our 2018 accomplishments. 

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Topics: clinical care LAMposium 2018 patient support Research        Categories: News

More Ways to Give: Qualified Charitable Distributions from IRAs

Posted on December 19, 2018   |   

Are you or someone you know over the age of 70 ½ and looking for more ways to give to The LAM Foundation? You may be able to donate through a Qualified Charitable Distribution! Read on to learn more about this opportunity to give.

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Topics: Donations IRA Qualified Charitable Distributions        Categories: News
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Short-Term Goals, Long-Term Effects: Outcomes of the 2017 LAM Patient Benefit Conference

Posted on November 30, 2018   |   

How can we improve the lives of LAM patients in five years or less? This is the question scientists, clinicians, and patients themselves gathered to answer at the first-ever LAM Patient Benefit Conference. Among the many valuable ideas shared, the following grant proposals have received funding to move forward. Each was chosen for its potential to result in solutions that will positively impact the diagnosis, care, or quality of life of LAM patients by the year 2023.

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Topics: Patient Benefit Conference Research        Categories: Events News
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Running for LAM: Q&A with Kat Steele

Posted on November 29, 2018   |   

Kat Steele is a LAM patient who commemorated the 5-year anniversary of her diagnosis by participating in the New Hampshire Marathon on September 29, 2018. Here, she shares insights from her journey as a LAM patient, as a runner, and as a fundraiser. 

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Topics: Fundraising        Categories: Events News
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