Min Hansen's Fundraiser
I'm Running for a Reason in the 2022 TSC NYC Marathon!
Yes, you read that correctly...I'm running in a marathon. Please help me support Dup15q Alliance and donate today
We are no longer accepting donations on this campaign, but there are other ways for you to support us today!
Isabelle Carman
"Go Dylan! You are the best. Thank you Min for the amazing race"
$100
A supporter of Min Hansen
I donated in support of this campaign.
$300
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Mark Halloram
"Great cause. Fab human!"
$100
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Sheena Makhecha
I donated in support of this campaign.
$50
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Scott and Sarah Taylor
I donated in support of this campaign.
$100
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Karla & Laurent De Greef
"Lots of love to the Kadner Reina’s. Best of luck for the marathon. We’ll be cheering on Central Park South!!!"
$200
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Anja Steinke
"Thank you Min! Here’s to Dylan! Anja, Austin, Anika and Tonie"
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christine col
"Love to Dylan and the entire fam. Y"
$50
A supporter of Min Hansen
I donated in support of this campaign.
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Bernardo Reina
"For Dylan and family !"
$100
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Bernardo Reina
"For Dylan and family. Way to go Min !!"
$100
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Mona Delank-Baker
"For Dylan"
$75
A supporter of Min Hansen
I donated in support of this campaign.
$500
A supporter of Min Hansen
I donated in support of this campaign.
A supporter of Min Hansen
I donated in support of this campaign.
$1,000
Suzanne Sands
"Suzanne Sands"
The St. Clair Group, Las Vegas
I donated in support of this campaign.
$500
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Amber Howard
I donated in support of this campaign.
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Noah Kadner
I donated in support of this campaign.
$250
Steve Kadner
"Kathy and Steve Kadner"
$250
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Monica Reina-Kadner
"Thank you Min! We are so proud and feel blessed that you are running for Dylan and creating awareness about this rare disease!"
I am excited to announce that I have signed up as a Charity Runner in the 2022 TSC NYC Marathon to support the Dup15q Alliance!
I know I said I'd never run a marathon. I meant it too, until I learned Dup15q Alliance was a charity partner for this year's NYC marathon. Dup15q Syndrome is extremely rare and characterized by a number of symptoms that may include, hypotonia, epilepsy, cognitive delay, motor delays, autism, and similar facial features.
I first became aware of Dup15q when I met our friends, Monica and Noah, years ago. Their youngest son, Dylan, is a Super Duper, having been born with the syndrome. For those of you who haven't had the good fortune of meeting Dylan - he gives the best hugs and has the happiest laugh. He loves Cookie Monster, swimming, and riding his bicycle. He gives our dog, Zoe, the softest pets whenever he sees her. Dylan is thriving, but it hasn't been easy for him or his family. There is no cure for Dup15q and, because it's so rare, it's often difficult for them to find the right medical and social resources. This is why organizations like Dup15q Alliance matter. Their mission is to provide family support and promote awareness, research, and targeted treatments for Dup15q Syndrome.
I will be taking on 26.219 miles of New York City streets on November 6th. Will I be setting any personal records? No, probably not. Will I potentially keel over somewhere along the route? Most likely yes. But it's going to be one heck of an experience.
Join me in supporting real change. Let’s support good in the world and make a difference.
Just a small donation will go a long way to helping me meet my goal for Dup15q Alliance.
To learn more about dup15q syndrome visit: https://dup15q.org/