For life well lived, today
We help youth with cystic fibrosis and chronic illnesses live like they’re illness-free.
A non-profit supporting children and young adults with chronic illness to pursue their dreams in the present.
Because why wait for wings to fly?
About Lea
A passionate advocate for quality of life
Lea Faraone was a nurse, public figure, and driven advocate who passed away at 28 due to cystic fibrosis. She believed no one should spend their time waiting for a cure, so we should do everything we can to improve their quality of life now.
Help young people with chronic illness live life to the fullest
Get Involved
Fly Me to the Moon
Recipient stories from the LMFF community
Our Key Sponsors
Learn more about living with chronic illness on our blog
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Meet our 2023 Blog Ambassador | Tyler Smith
What comes to mind when we here to words, “we need to […]
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Chronic Illness and Mental Wellness
Our returning Blog Ambassador, Kasey Seymour, who underwent double lung transplant surgery […]
The Vision In Action
Our Mounting Impact
16+
Over 16 Fly Me to the Moon grants awarded—and counting
$210,000+
Over $210,000 worth of medical equipment and supplies donated
$120,000+
Over $120,000 raised for a cystic fibrosis cure
Fly Me to the Moon Stories
Meet a Few of our Past Recipients
Why Wait for Wings?
Find support or contribute to our initiatives
Discover all the ways you can get involved with the LMFF mission.