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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

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

  • Logan

    Logan

    Logan was diagnosed with CF through prenatal screening. While Logan has been […]

    Learn More

  • Noah

    Noah

    Nine-year-old Noah is a baseball enthusiast with a lot of energy. He […]

    Learn More

  • Landon

    Landon

    Landon’s journey with Cystic Fibrosis began at just three weeks old when […]

    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

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leamariefaraonefoundation

Today is #GivingTuesday. 🙏 This is a day to su Today is #GivingTuesday. 🙏 
This is a day to support Lea’s mission. This is a day to make a difference in someone’s life. This is a day to give back because so many of us have so much in our lives to be grateful for. 

Every donation big and small counts. This year, we’d like to THANK YOU for making a donation so for every $50 donation you make, you’ll receive either an LMF Foundation hat, t-shirt, or a mug. Select the item of your choice when making your donation via the link in our bio!

Share this post with someone who can help us make a difference this year! 🩷
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#givingtuesday #giveback #givingseason #makeadifference #donatenow #nonprofit #medicalnonprofit #makeadifference #givehope #bethechange #CysticFibrosis #CFWarrior #CFAwareness #CureCF #CFCommunity #BreatheEasy #FightCF #CFAware #CFResearch #CFAdvocacy #leamariefaraone #leamariefaraonefoundation
Tomorrow is Giving Tuesday, a day to come together Tomorrow is Giving Tuesday, a day to come together and make a real difference. 🙏🩷 It’s not just about helping children—it’s about lifting up entire families, giving them the chance to build a better life. If you’re a parent in need, please don’t hesitate to reach out—we’re here for you. And if you’re a parent who can lend a hand, your support this month can truly change lives.
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#givingtuesday #giveback #makeadifference #givingseason #donatenow #nonprofit #philanthropy #bethechange #togetherwecan #givehope #CysticFibrosis #CFWarrior #CFAwareness #CureCF #CFCommunity #BreatheEasy #FightCF #CFAware #CFResearch #CFAdvocacy #baltimorenonprofit #leamariefaraone #leamariefaraonefoundation
Sharing a few things we're thankful for today and Sharing a few things we're thankful for today and everyday. 🩷🙏 From our family to yours, wishing you a Happy & Healthy Thanksgiving. 
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#thankfulgratefulblessed #ThankfulThursday #Thanksgiving #cfcommunity #leamariefaraone #leamariefaraonefoundation
This Giving Tuesday, make a difference that lasts This Giving Tuesday, make a difference that lasts a lifetime. 🙏 Your support helps us continue our mission of helping children and young adults living with chronic illnesses like cystic fibrosis live a better quality of life. Together, we can make a difference. 

Save this post so you remember to give back on December 3! Now share this post with someone so we can make an impact together this year. 🙌🩷
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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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