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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 [email protected].
  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

We’ve had some more wings spotted! 🪽 Our social m We’ve had some more wings spotted! 🪽

Our social media manager Kayleigh was touring a pumpkin patch in Black Creek, British Columbia, Canada and found these beautiful wings that instantly reminded her of Lea & our recent Chalk Walk event! 🧡🇨🇦

Every pair of wings, whether handmade, spotted, or sent from near or far, is another beautiful reminder of Lea and the legacy that continues to travel with us.

And just a reminder: our wings campaign isn't limited to summer! You can send us your wings any time of year! 📸 DM us or email a photo to LeaMarieFaraoneFoundation@gmail.com with your name and where you found (or made!) them.

We can’t wait to see how far Lea’s legacy travels 🦋
A day filled with butterflies, community, and so m A day filled with butterflies, community, and so much love, that’s what Chalk Walk is all about 💜🦋

Our 7th Annual Chalk Walk was one to remember! We saw familiar faces and new families who joined us for the first time. It was incredible to see everyone come together to celebrate Lea’s legacy and raise awareness for Cystic Fibrosis.

Over 520 butterflies filled the pavement at Hunt Valley Towne Centre, each one a beautiful reminder of the love, hope, and support that continues to surround this community.

To everyone who helped make this day possible, thank you for being part of something so special. We couldn’t do it without you! Our sponsors, Hunt Valley Towne Centre, our volunteers… each and every one of you truly help us make a difference.

Now, let’s relive a little of the magic from this year’s Chalk Walk 🎥💜
Now that we’ve had a chance to process the weekend Now that we’ve had a chance to process the weekend, we are so incredibly grateful for the absolute success that was our 7th Annual Chalk Walk! 💜🦋

We met so many new families and spread so much more awareness of LMFF and the families we support. And together, we drew over 520 butterflies across Hunt Valley Towne Centre in honor of Lea and those living with Cystic Fibrosis and CF-related illnesses!

It was also so special to have our 5th Women in Science Scholarship winner, Maggie, volunteering with us at the event. Seeing the next generation show up for this community was incredible 💫

To everyone who drew, donated, volunteered, sponsored, and cheered us on, whether in person or from afar: thank you. You helped us fill the pavement with hope, and you’re the reason Lea’s legacy keeps living on.

Stay tuned, because our official Chalk Walk reel is coming soon! 🎥 But for now, swipe through to see some of our favorite memories from the day 💜🦋
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! 💜

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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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