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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

There’s less than one month until our 7th Annual L There’s less than one month until our 7th Annual LMFF Chalk Walk!

Take a look back at last year's Chalk Walk that we filled with color, the community, and joy in Lea's honor 💜

With the butterfly-covered pavement and the laughter-filled afternoons with family, this event is one of our favorite days of the year. And we're just getting started on making this year even bigger.

📅 Save the date: October 17 | 10AM–4PM
📍 Hunt Valley Towne Centre, Center of Main Loop
🌧️ Rain Date: October 18

Who's ready to fill Hunt Valley Towne Centre with color again? 🎨
Another LMFF Mission accomplished! The latest Fly Another LMFF Mission accomplished! The latest Fly Me To The Moon grant has officially launched! 🚀🌕

Our LMFF Advisory Council is honored to have awarded medically necessary therapy to a 4-year-old grant recipient from Georgia living with a chronic illness, helping advance her quality of life and giving her family a little more freedom to simply enjoy being together.

At the family's request, we're keeping her story private, but they wanted to share their heartfelt thanks with all of you:

"Thank you to the LMFF team, our sponsors, our donors, and everyone who follows and supports this mission. Your generosity means more than words can say."

This is exactly why we do what we do. Every grant, every donor, every one of our supporters, you're part of what makes moments like this possible 💜

Here's to more launches ahead 🔭🦋
Why do we paint the pavement with chalk butterflie Why do we paint the pavement with chalk butterflies every year? 🦋💜

The Chalk Walk isn't just a fun family event. It's one of the most visible ways we bring cystic fibrosis and CF-related illness awareness into the community. Every butterfly drawn on the ground represents a life touched by CF, a message of hope, and a reminder that no one should have to wait for wings to fly.

This year marks our 7th Annual Chalk Walk, and every single one has been a testament to what community can do when it shows up for each other.

📅 October 17 | 10AM–4PM
📍 Hunt Valley Towne Centre, Center of Main Loop
🌧️ Rain Date: October 18

Come paint the pavement with purpose this October 💜 The more butterflies we draw, the more support and donations we receive.
Say hello to the Butterfly Catcher 🦋 This is one o Say hello to the Butterfly Catcher 🦋 This is one of the brand new children’s activities at this year's Chalk Walk and we are SO excited to debut it!

Little ones will get to toss butterflies into the catcher and see how many they can land. How adorable (and fun!) is that?!

Bring the whole family and let the kids play their way through a day made for community, color, and connection 💜

📅 October 17 | 10AM–4PM
📍 Hunt Valley Towne Centre, Center of Main Loop
🌧️ Rain Date: October 18

See you on the pavement! 🎨

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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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