Miles for Hope - Lacing up for Levi
Nevus Outreach / Miles for Hope
With each step of the Boston Marathon, we raise awareness for those living with CMN, NCM, and related conditions.
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$14,079
Raised
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$18,500
Goal
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151
Supporters
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62
Days Remaining
Recent Transactions
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Jennifer Pond
$26.00 / 2 days ago
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Carrie Coughlin
$124.80 / 5 days ago
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Amanda Chaves
$26.00 / 9 days ago
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Joanny Bauer
$52.00 / 9 days ago
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Anonymous
$52.00 / 9 days ago
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Lisa L Dean
$156.00 / 9 days ago
We love you guys and are so happy the Levi is doing so well. It is great that you have this wonderful organization to be there for all who need it. ❤️ NC Deans
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Lelia Boniadi
$52.00 / 10 days ago
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Corrie Murphy
$5.20 / 10 days ago
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Anonymous
$104.00 / 11 days ago
RUN VUTO RUN!!!! Lots of love to Levi and everyone living with CMN ❤️
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William S. Brady
$260.00 / 11 days ago
For a handsome boy who’s facial difference doesn’t take away from his spirit or his smile.
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Kathy Twyman
$104.00 / 11 days ago
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Brittney Jenkins
$26.00 / 12 days ago
You’ve got this, Vuto! Sending lots of luck and a great race for Levi☘️🏃♂️
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Carol Hannon
$26.00 / 17 days ago
Wishing you a great race, Levi’s cure and success in fund raising.
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Caroline Hill
$10.40 / 17 days ago
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About Miles for Hope - Lacing up for Levi
Miles for Hope - Lacing up for Levi
On April 20th, Michael will proudly wear a Boston Marathon charity bib and run his first marathon ever for his son Levi through Nevus Outreach!
Nevus Outreach is the nonprofit organization that represents Levi’s disease, which is called Congenital Melanocytic Nevus. This organization’s mission is to raise awareness, fund research, and provide advocacy and support for individuals and families affected by CMN and NCM (neurocutaneous melanosis).
This diagnosis is so rare that many people go their entire lifetimes without seeing it or hearing about it. We have made it our mission to embrace, celebrate and share his visible difference to make the world a more accepting, inclusive, and ultimately kind place for Levi and all individuals who have these significant visible skin differences.
We attended the 2024 Nevus Outreach conference with Levi when he was only 3 months old and it changed our life. It is Mike’s honor to run for this organization and help raise money that will directly help their cause.
We hope that through your donation, we can reach far and wide with the message to support those impacted by CMN and NCM. The more people who know about this disease outside of the Nevus community, the more people who can rally behind the cause.
Thank you.
Leslie, Michael, and Levi
If you would like to learn more about CMN please visit nevus.org