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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

🦋 MARK YOUR CALENDARS! 🦋 The 7th Annual Chalk Wal 🦋 MARK YOUR CALENDARS! 🦋

The 7th Annual Chalk Walk is coming back to Hunt Valley Towne Centre on October 17th from 10AM until 4PM! 💜

For the last 7 years, our community has come together to fill the pavement with butterflies in honor of Lea and help support children and young adults living with Cystic Fibrosis and CF-related illnesses. Every butterfly drawn helps us continue making a difference, and we can’t wait to see the sidewalks come to life again this year.

Bring the family, get creative, enjoy face painting and children’s activities, and help us make our 7th year another special one!

📅 October 17 | 10AM–4PM
📍 Hunt Valley Towne Centre, Center of Main Loop (aka ‘The Valley’!)
🌧️ Rain Date: October 18 | 10AM–4PM

Save the date and stay tuned for more details as we get closer! 🦋
Lea had a way of finding something meaningful in e Lea had a way of finding something meaningful in every experience, even the difficult ones 💜

“I am so thankful for all the good and bad experiences I’ve had this year because it’s taught me more about myself than I could have ever imagined.” – Lea

Her words are a reminder that growth doesn’t always come from the moments we would choose for ourselves. Sometimes it’s the challenges, the unexpected turns, and everything in between that teach us the most about who we are.

Through it all, Lea continued to learn, grow, and embrace the life in front of her.

A little reminder from Lea to be grateful for the whole journey, not just the easy parts 🦋
There’s a reason we call it Lea’s Butterfly Bush 🦋 There’s a reason we call it Lea’s Butterfly Bush 🦋💜

Every summer, this bush comes to life with butterflies, and there’s something so special about watching them gather, flutter, and stay awhile.

Butterflies have become such a meaningful reminder of Lea to our family, and moments like this have a way of making her feel just a little bit closer 🦋

#WhyWaitForWings
🪽 Another special wing sighting for our #WhyWaitFo 🪽 Another special wing sighting for our #WhyWaitForWings map! 🦋

Lea’s second cousin Liam and his mom, Casie, spotted these wings in Harrisburg, Pennsylvania and made sure to send them our way 💜

We love seeing Lea’s family join in and help us continue filling the map. Every new sighting, whether it’s close to home or miles away, is another beautiful reminder of Lea and the legacy that continues to travel with us.

Thank you, Liam and Casie, for keeping your eyes out for wings and sharing this special find!

Have you spotted wings lately? 📸 Send us a photo in a DM or email it to LeaMarieFaraoneFoundation@gmail.com with your name and where you found them.

Where will Lea’s wings show up next? 🦋💜

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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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