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Judah's Cranial Journey

$5,293 of $5,000 goal

Raised by 56 people in 4 months
Created September 12, 2018
Fundraising Team
on behalf of Lacey Hoffman
I am Judah's grandmother. Judah and his parents Justin and Lacey Hoffman live in Cook, Ne.  At birth, my grandson Judah Hoffman was born with a rare condition called Metopic Craniosynostosis. This condition causes the soft spot on the front of his skull to close early, requiring surgery in infancy to reopen the soft spot and allow his brain to grow properly. Because of how rare the condition is, Justin and Lacey will be traveling to San Antonio in October to have it done. This page is set up to help with the additional medical and travel expenses required for our sweet grandson. We so appreciate all of the support and love they have received and are continuing to believe in God’s faithfulness.
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Update 1
Posted by Lisa Burianek
4 months ago
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Judah's Cranial Journey has reached 50% of its goal. Thanks to Aaron, Latscha and JR.
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$5,293 of $5,000 goal

Raised by 56 people in 4 months
Created September 12, 2018
Fundraising Team
on behalf of Lacey Hoffman
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BS
$100
Brad & Andrea Smith
2 months ago
JH
$50
Jeff & Melinda Holstine
3 months ago
KG
$20
Kelsey Gash
3 months ago
$50
John and Kimberly Brady
3 months ago
CB
$1,500
Cody Ball
3 months ago
DH
$100
Dan and Elaine Hanson
4 months ago
$100
Brenda Lutz
4 months ago
$50
Anonymous
4 months ago
LR
$100
Laura Redoutey
4 months ago
JD
$50
Jessica Distefano
4 months ago
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