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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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Fly Me to the Moon

A grant program for young people affected by cystic fibrosis and other chronic illness.

About the grant

Providing care that enhances life

Those with chronic illnesses often need special equipment and resources to keep their health to the highest standards. Fly Me to the Moon provides young beneficiaries with the tools needed to live life to the fullest so they know they are more than their illness.

  • Medical equipment
  • Home health care
  • Adjunct therapy
Apply for the grant

Grant Eligibility

Fly Me to the Moon is available to those who:

  • Are a child or young adult diagnosed with a chronic illness and in need of a medical intervention that will significantly improve that individual’s quality of life.
  • Have completed the Fly Me To the Moon Grant Application, Medical Care Team Letter of Referral, and current prescription or sufficient documentation for the medical device or service needed.
  • *At this time, pharmacological therapies are not eligible for fulfillment under the Fly Me to the Moon grant.
  • Physician referral must be from a physician practicing in the United States of America.
Start the application

Before you apply

The Fly Me to the Moon Grant provides assistance to children and young adults living with chronic illness. Before completing the full application, please review the eligibility requirements below.

Applicants must meet the following criteria:

  • Age: The potential grant recipient must be between 0 and 26 years of age.
  • Chronic Illness: For purposes of this grant, the potential recipient must be living with a diagnosed chronic illness. This includes, but is not limited to, individuals with cystic fibrosis (CF) or CF-related mutations.
  • Grant Request: Funding may be requested for medical equipment, adjunct therapies, or home health needs that support the individual’s medical care and quality of life.
  • Grant Limit: At this time, each eligible individual may receive one grant award from the Lea Marie Faraone Foundation.

How to apply

We look forward to playing amongst the stars with you! To apply, please follow these steps:

  1. Download and complete the Fly Me to the Moon Grant Application
  2. Obtain a letter of referral from a member of your medical care team (i.e. physician, social worker, etc.) stating why you need the medical device or service applied for. A signature and date are required.
  3. If selected as a beneficiary, LMFF will request a prescription or other sufficient documentation where appropriate for the medical device or service applied for. *If such documentation cannot be produced, eligibility for the grant may be forfeited.
  4. Please send both the completed Fly Me to the Moon Grant Application and the medical care team letter of referral to leamariefaraonefoundation@gmail.com.
  5. Submission of this application grants permission for the Lea Marie Faraone Foundation to email you.
Apply Today

Fly Me to the Moon Stories

Meet our Fly Me To The Moon Grant Recipients

  • Maddox

    Maddox

    Meet our newest Fly Me To The Moon grant recipient: Maddox Duffey 🌕💫 Maddox is a little fighter living with cystic fibrosis, and we’re honored to support his family through our Fly Me To The Moon Grant. After navigating insurance challenges and rising medical costs, Maddox’s family was left facing a significant financial burden for…

    Learn More

  • Ray

    Ray

    Ray is a 17-year-old living with Spinal Muscular Atrophy Type 1 (SMA), a progressive neuromuscular disease that causes severe muscle weakness. Diagnosed at just five months old at Children’s Hospital of Philadelphia, Ray has faced countless medical challenges with strength, resilience, and an incredible outlook on life. Despite it all, Ray continues to thrive. He…

    Learn More

  • Cooper

    Cooper

    Cooper Pike was diagnosed with Cystic Fibrosis at just 17 days old through newborn screening.Cooper is now 2.5 years old with daily treatments, a loving supportive system and his unstoppable energy. Cooper is living each day with courage, curiosity, and heart. He loves t-ball, football, running and jumping on his trampoline. Cooper’s Mom advocated for…

    Learn More

View All Recipients

Why Wait for Wings?

Apply for Fly Me to the Moon

If a young person you know is eligible for our grant program, we invite you to apply and share your story. We can’t wait to hear from you!

Apply Now

Follow Us

TODAY'S THE DAY! 🦋 The 7th Annual Chalk Walk has TODAY'S THE DAY! 🦋

The 7th Annual Chalk Walk has kicked off at Hunt Valley Towne Centre and we’re here until 4PM!

Bring your family, grab some chalk, and help us paint the pavement in honor of Lea and everyone living with cystic fibrosis and chronic illness.

📍 Hunt Valley Towne Centre, Center of Main Loop

🎨 Butterfly chalk art zone

💜 Face Painting & Children’s Activities

 📣 Meet the LMFF team + learn about the programs your support powers

Can't make it? You can still take flight with us and support our cause. Donate $10 online and we'll write your name on a butterfly for the day 🦋

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

See you today at Hunt Valley Towne Centre! 💜
📣 Special shoutout to The Greene Turtle Hunt Valle 📣 Special shoutout to The Greene Turtle Hunt Valley for supporting the 7th Annual Chalk Walk once again! 🦋

Here’s how they’re helping us make this year even bigger:

🍔 Donating 20% of sales on October 17 (just show or mention the flyer!)
🎟️ Hosting a raffle with a Greene Turtle gift basket at the Chalk Walk
🦋 Selling Butterfly Bundle butterflies in store

Every bite, raffle ticket, and butterfly helps us continue supporting children and young adults living with cystic fibrosis and CF-related illnesses 💜

Thank you, Greene Turtle, for being such a wonderful part of our community and for helping us carry Lea’s legacy forward 💫

📅 October 17 | 10AM - 4PM
📍 Hunt Valley Towne Centre, Center of Main Loop
🌧️ Rain Date: October 18
Every butterfly on the pavement starts with a piec Every butterfly on the pavement starts with a piece of chalk, and this year, all of it is thanks to the Towson Elks Lodge #469! 🦋

We are so grateful to the Towson Elks for providing all of the chalk for our 7th Annual Chalk Walk. Because of their generosity, every family, friend, and neighbor who joins us can grab a piece of chalk and help fill Hunt Valley Towne Centre with butterflies in honor of Lea 💜

Their support helps us keep sharing Lea’s story, raise awareness for cystic fibrosis and CF-related illnesses, and empower families through the Fly Me To The Moon Grant and other LMFF initiatives and awareness campaigns.

Thank you, Towson Elks, for helping us paint the pavement with purpose this weekend 💫

📅 October 17 | 10AM - 4PM
📍 Hunt Valley Towne Centre, Center of Main Loop
🌧️ Rain Date: October 18
The countdown is ON… we're just 5 DAYS away from f The countdown is ON… we're just 5 DAYS away from filling the streets with color, community, and hope 🦋

Whether you'll be joining us in person or participating from afar, this is your reminder to grab your chalk, spread Lea's message, and help raise awareness for cystic fibrosis and CF-related illness.

📅 October 17 | 10AM–4PM
 📍 Hunt Valley Towne Centre, Center of Main Loop
 🌧️ Rain Date: October 18
 🎨 Butterfly chalk art zone
 💜 Face painting & Children’s Activities, including our brand new butterfly catcher game!
 📣 Meet the LMFF team + learn about the programs your support powers

Let's make our 7th Chalk Walk the most vibrant one yet 💜 The more butterflies drawn, the greater support we receive!

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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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