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Featured Article

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Zooming-In on What Matters: Education. Connection. Hope.

Posted on April 16, 2021   |   

March 2020. LAMposium as we know it is cancelled. May 2020. LAMposium in Your Living Room goes viral. Whoops, that is, virtual.

Last spring, when it became clear to us that we would not be gathering as a LAM community in Cincinnati, we at the Foundation quickly shifted our focus to designing virtual experiences that would capture the key elements of our beloved LAMposium. It is this vision that frames our virtual educational series, Read More

Topics: LAMposium in Your Living Room        Categories: Educational Resources

Recent Articles

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Save the Date: Breath of Hope Day of Giving!

Posted on July 31, 2019   |   
Author: A. Bloomer

Save The Date: Thursday, September 12, 2019. That’s the date of our Breath of Hope Day of Giving, a 24-hour fundraising experience and the first of its kind for The LAM Foundation. It promises to be a day filled with information, entertainment, and giving.  

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Topics: #FilltheFeather DayofGiving FundACure        Categories: Events
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Welcoming New Faces to The LAM Foundation

Posted on July 31, 2019   |   
Author: A. Bloomer

We are very excited to be welcoming a new member to The LAM Foundation team as well as congratulating a current one on a new role! Join us in giving them each a very warm welcome. 

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Categories: News
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Fundraising Simplified: Francine Kalogerou

Posted on July 24, 2019   |   
Author: A. Bloomer

Francine Kalogerou was diagnosed with LAM in February 2019 and instead of letting that define her, it helped her find a new perspective on life. In her own words, "I don’t know what the future holds for me, but I do know I have today. Yesterday is gone. The future hasn't happened yet. Looking at life and my situation positively is making all the difference in the world." With this positivity, Francine decided to take action and host a walk-a-thon benefiting The LAM Foundation. 

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Topics: Fundraising LAMChampion        Categories: Events
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Fundraising Simplified: Elizabeth Hardy

Posted on July 16, 2019   |   
Author: A. Bloomer

For her birthday, Elizabeth Hardy decided that instead of receiving gifts from her friends and family, she wanted to do something with a little more meaning. It was a big birthday for Elizabeth as she was not only turning 60, but it was also the 25th year since receiving her LAM diagnosis. She wanted to take this opportunity to ask her closest friends to join her for a brunch to celebrate and donate to The LAM Foundation as their birthday “gift”. Much to Elizabeth’s surprise, nearly everyone she told about her fundraiser sent a donation to The LAM Foundation in her honor.  

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Topics: Fundraising LAMChampion        Categories: Events
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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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