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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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Let’s improve the quality of the present

Discover how to find support or get involved with our initiatives.

Grant for Families

Fly Me to the Moon

Fly Me to the Moon is a grant that helps families and individuals affected by chronic illness, such as cystic fibrosis, access the 5-star medical care they need. Whether it’s medical equipment, home health, or adjunct therapy, we’re here to help make dreams a reality.

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Fly Me to the Moon Grant

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Support our mission of providing life-changing care and equipment to youth with chronic illnesses

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Give the gift of a brighter present

Donations are always open to help improve the quality of life for young people with chronic illnesses. See the direct impact of your contributions as children and young adults gain access to transformative treatments and resources.

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Scholarship

Women in Science

Each year, we award a $5,000 scholarship to a graduating senior at Notre Dame Preparatory School who is entering college studies in science, medicine, nursing, or scientific research.

Meet our Scholarship Recipients

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Another pair of wings has found its way onto our # Another pair of wings has found its way onto our #WhyWaitForWings map! 🦋

A big thank you to Courtney for sending us this beautiful set of vibrant yellow wings from Sandbridge Beach, Virginia! ☀️🌊

Every wing sighting shared with us is a reminder that Lea’s legacy continues to spread far beyond where it all began. It’s amazing to see our map grow with each photo, each story, and each person helping us keep Lea’s spirit flying high.

Heading out on an adventure this summer? Keep an eye out for wings wherever you go! They can be found in murals, artwork, nature, sculptures, and all kinds of unexpected places.

📸 If you spot a pair, send us a photo along with your name and location at LeaMarieFaraoneFoundation@gmail.com, or DM us!

Where will Lea’s wings take us next? 💜
Every year around Lea’s birthday, the Faraone fami Every year around Lea’s birthday, the Faraone family gathers for one of our most cherished traditions.

A holiday spent together at the beach 🌊💜

It’s a time to laugh, reminisce, share stories, and celebrate the incredible life Lea lived. While we miss her every single day, this trip reminds us that her love continues to bring us together and that her legacy lives on through the memories we share, the lives we touch, and the moments we create as a family.

These trips are filled with so much more than sunshine and ocean views. They’re filled with gratitude, connection, and the promise to keep carrying Lea’s light forward.

Here’s to another year of celebrating Lea the way she would have wanted, with family, laughter, and making memories together 🦋

Happy Heavenly Birthday, Lea. You’ll always be the heart of our family 💜
One of the core missions of the Lea Marie Faraone One of the core missions of the Lea Marie Faraone Foundation is to bring greater awareness to chronic illnesses like cystic fibrosis. One of the simplest ways we can do that is by sharing what life with CF can really look like. 💜

Did you know that managing cystic fibrosis is much more than taking medication?

Every person with CF has a unique treatment plan, but daily care often includes:
🫁 Airway clearance therapy to help loosen and clear mucus from the lungs.
💨 Inhaled medications to open the airways, thin mucus, and help prevent or treat lung infections.
💊 Pancreatic enzymes with every meal and snack to help the body absorb nutrients, along with specialized vitamins.
🏃‍♀️ Regular physical activity to support lung function, energy, and overall health.
🧬 CFTR modulators for those with eligible gene mutations, helping target the underlying cause of CF.

Living with cystic fibrosis means dedicating hours each day to treatments that most people never have to think about. By learning more about CF, we can better understand the resilience of those living with it and the importance of continued research, care, and support.

Awareness starts with understanding. 💜
This July, we’re celebrating what would have been This July, we’re celebrating what would have been Lea’s 36th birthday. A month dedicated to honoring her life, her legacy, and the incredible impact she continues to have 🎂💜

To celebrate, we’re inviting our community to take part in our $36 for 36 campaign by making a $36 donation in Lea’s memory.

Your gift helps us continue the work that meant so much to Lea, providing Fly Me To The Moon Grants, Women in Science Scholarships, Advocacy & Awareness, and support for children, young adults, and families navigating chronic illness.

Every dollar helps carry Lea’s legacy forward. Every act of generosity helps someone feel seen, supported, and hopeful 🪽🦋

Donate here 🔗 https://www.paypal.com/donate/?hosted_button_id=RVH6M8JTWA5DC

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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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