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Lea Marie Farone Foundation

Lea Marie Farone Foundation

Helping children and young adults with chronic illness do the things they dream of doing.

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Meet the Lea Marie Faraone Foundation

Cultivating courage, fostering freedom

Our Story

Taking Flight

Our Story

When young Lea Marie Faraone was diagnosed with cystic fibrosis, everything changed for her family. Suddenly, they had to think through each detail of their lives in terms of CF. Despite their fears and questions, they decided to live as “normally” and fully as possible.

As Lea grew older, she embraced this mindset. She became a public figure and a passionate advocate who lived the life she wanted, touching thousands of other lives along the way. She dreamt of creating her own foundation that would help improve quality of life for young people with CF and other chronic illnesses.

Lea passed away on December 13, 2018 while waiting for a transplant, but her vision forges forward today. The Lea Marie Faraone Foundation was born to fulfill her dream of helping others with chronic illness live life to the fullest each day, rather than waiting for a cure. Because no one should wait for wings to fly.

Our Impact

Improving the Quality of the Present

We help children and young adults with chronic illness do the things they dream of doing, big and small.

Grant Recipients icon

Grant recipients gain access to cutting-edge treatments that enhance life, instead of hindering it.

Fundraising Events

Fundraising events build community while benefitting grant recipients and medical research.

Scholarships

Scholarships empower young women making a difference in medicine and science.

Why Wait for Wings?

What We Believe In

number 1

There’s power in community

We want families to feel like they have a trusted place to go whenever they’re looking for support. When you’re in our circle, you’re part of the LMFF family too.

number 2

Where there’s a will, there’s a way

We believe those with chronic illnesses should do the same things we all do. Sometimes it requires a little creativity and innovation but, together, we can make it happen.

number 3

Immediate impact on quality of life

Our programs provide life-changing outcomes in the short term. You can see the result of donations as young people embrace more of the everyday things that make life beautiful.

Meet The Team

A family-founded organization

We embrace our initiatives with our whole hearts and souls. Since we’re completely volunteer-run, every dollar goes straight to the mission.

Laura O'Donnell

Laura O’Donnell

Mother to Lea / Executive Director / Co-Founder

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Laura O’Donnell

Besides her most important role of being a CF mom to Lea, Laura brings to the table more than 25 years of executive leadership in healthcare, working with major organizations such as Johns Hopkins Medicine, MedStar Health and Genesis Healthcare. Laura holds a Masters from University of Maryland Baltimore. As director, Laura has a key focus on bringing Lea’s plans, legacy, and mission to life.

Leeza Farone

Leeza Heitzman

Sister to Lea / Co-Founder / Director of Marketing & Programs

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Leeza Heitzman

Leeza has a lifetime of experience being a sister to CF fighter, Lea. She also brings a background of clinical research from Johns Hopkins University of Medicine and a degree in biochemistry from Mount St. Mary’s University. Recently, she has embarked on a new journey as a physician assistant student at the Anne Arundel Community College/ University of Maryland Baltimore Collaborative PA Program. She plans to graduate with her Masters and PA licensure by 2021, with hopes to give back her new-found medical knowledge to the Lea Marie Faraone Foundation.

Henry Faraone

Henry Faraone

Father to Lea / Co-Founder / Director of Finance & Operations

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Henry Faraone

Henry is a superhero when it comes to being a CF dad to Lea. He continues to give back to the community with more than 18 years’ experience as a teacher for students with special needs at Sheppard Pratt Health System. He holds a certification in special education from the University of Maryland University College. Henry has committed himself to drive Lea’s legacy with the Lea Marie Faraone Foundation to a national level.

Why Wait for Wings?

Find support or contribute to our initiatives

Discover all the ways you can get involved with the LMFF mission.

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Follow Us

Another beautiful pair of wings has found its plac Another beautiful pair of wings has found its place on our #WhyWaitForWings map! 🦋

These wings were spotted in Paris, France by Lea’s uncle, Dr. Richard Leupold, while on vacation 🇫🇷 It’s incredible to see Lea’s legacy reaching across the globe, with each new wing sighting serving as a reminder of the love, hope, and kindness she continues to inspire.

Thank you, Richard, for sharing this special find with us. 💜

Have you spotted a pair of wings this summer? We’d love to add them to our map!

📸 Send us your photo by email at LeaMarieFaraoneFoundation@gmail.com or simply send it to us in a DM. Don’t forget to include your name and where you found them!

Let’s keep filling the map and celebrating Lea’s beautiful legacy, one pair of wings at a time 🦋
Have you spotted any wings this summer? 🦋 Our #Wh Have you spotted any wings this summer? 🦋

Our #WhyWaitForWings map is growing, and we’d love to add your wing sightings!

Whether you’re traveling across the country or exploring your own hometown, keep an eye out for wings. Murals, sculptures, artwork, nature, and unexpected places can all remind us of Lea and the legacy she continues to leave behind.

📸 When you find a pair, send us:
- A photo
- The location
- Your name (if you’d like us to include it)

You can:
📧 Email your photo to LeaMarieFaraoneFoundation@gmail.com
OR
💌 Send it to us in a DM right here on Instagram or Facebook!

We’ll feature your photo and add it to our growing #WhyWaitForWings map.

Let’s see how many places Lea’s wings can reach this summer. We can’t wait to see where you find them next! 🦋💜
One of the greatest gifts Lea left behind was her One of the greatest gifts Lea left behind was her perspective.

Even while living with cystic fibrosis, she chose to focus on what she could do, embracing life with gratitude, courage, and joy.

“The happiest people don’t have the best of everything, they just make the best of everything.”

Those words continue to guide the work we do and remind us to make the most of every moment.

💜
Sometimes, the smallest moments leave the biggest Sometimes, the smallest moments leave the biggest impact and this one is no exception 🪽 💜

Because of the generosity of our supporters, Maddox is receiving his new AffloVest, a life-changing piece of equipment that will help make his daily cystic fibrosis treatments more comfortable and give him greater freedom to simply be a kid.

Along with his new vest, Maddox also received his Fly Me To The Moon wings, a reminder that he has an entire community cheering him on every step of the way.

To everyone who has donated, sponsored an event, attended a fundraiser, or supported the Lea Marie Faraone Foundation in any way, thank you. Your generosity makes moments like this possible. To @afflovest , thank you for allowing us to continue to improve the lives of so many who are suffering from this terrible disease. We couldn’t do it without you!

Watching Maddox’s smile says it all 💜

Here’s to helping more children and young adults living with chronic illness spread their wings and live life to the fullest.

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The Lea Marie Faraone Foundation is a 501c(3) providing life changing opportunities to children and young adults fighting chronic illness so they may live as if they are illness-free.


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P.O. Box 20396, Towson, MD, 21284, US
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