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Mia Moo Fund

Organized by Carrie McCoy
Front large extended
Mia Moo Fund Fundraiser - unisex shirt design - front
Mia Moo Fund Fundraiser - unisex shirt design - back
Mia Moo Fund shirt design - zoomed
Gildan Youth Ultra Cotton T-shirt

Buy a shirt to help our cause!

Custom Ink
All funds raised will go to Carrie McCoy, the organizer for Mia Moo Fund.
$570 raised
34 items sold of
50 goal
Thanks to our supporters!
$20
Gildan Youth Ultra Cotton T-shirt, Unisex - Jade Dome
Gildan Youth Ultra Cotton T-shirt
Unisex - Jade Dome
Organized by Carrie McCoy

About this campaign

Every kid deserves a smile. By purchasing this shirt, you are helping to fund research, raise awareness, and help those in need. This is one of two designs that is available in youth and adult sizes. This fundraiser ends February 8th and the shirts will be delivered about 2 weeks after that time. You can have your child wear this on the day of Jonathan's surgeries, if you'd like. I will post the details of his surgeries on the blog: http://unspeakablejoymovement.blogspot.com . Please share this fundraiser with your family and friends. Thank you for your support and God bless!

IMG_27321JPGEvery 4.5 minutes a U.S. baby is born with a birth defect according to Coleen Boyle, director of the National Center on Birth Defects and Developmental Disabilities at the Centers for Disease Control and Prevention in Atlanta. Birth defects account for about 20 percent of mortality in the first year of life. In addition, babies born with birth defects have a greater chance of illness and long-term disability than babies without birth defects, Boyle said. "Most of us know someone affected by these conditions - a child born with cleft lip and palate; a young girl with Down syndrome; a co-worker who has lost a baby due to a severe heart defect," Boyle said in a statement.

There are 4437 babies born with cleft lips annually and 2651 babies born with a cleft palate. It is the fourth most common birth defect in the United States. Our son, Jonathan, was born with a severe bilateral cleft lip and palette. He is in the early stages of repairing it. Our goal is to brin awareness to this while raising funds to help other families through the Mia Moo Fund. Consider purchasing a t-shirt today. You can wear it when Jonathan has his surgeries. We will share his surgery dates with you on the blog.  

Supporters

Abbey Mueller 4 items

Carrie McCoy and her family used to part of our church family and we just really appreciate her and her family.

McCoy Kids 6 items
Lauren McCoy 1 item
Melinda Nelson 2 items

We have a 2 1/2 year old granddaughter that was born with a clef lip and pallet. She lives with us now and is doing amazing but has a long road ahead of her. May God Bless you!

Carrie McCoy 1 item
J Darr 1 item

Encouraged to see how you are seeking to serve others as you also walk through this.

Terry Abramson 1 item
Holly Smith 1 item
Anonymous 1 item

What a great cause! I love how God is using you and little Jon to reach others! Love you friend!

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