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Emery's Army: Sturge-Weber Awareness

Organized by Joy Elise Davis
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Emery's Army: Sturge-Weber Awareness Fundraiser - unisex shirt design - front
Emery's Army: Sturge-Weber Awareness Fundraiser - unisex shirt design - back
Emery's Army: Sturge-Weber Awareness shirt design - zoomed
Emery's Army: Sturge-Weber Awareness Fundraiser - unisex shirt design - front
Emery's Army: Sturge-Weber Awareness Fundraiser - unisex shirt design - back
Emery's Army: Sturge-Weber Awareness shirt design - zoomed
Gildan Ultra Cotton T-shirt

Profits from all shirts go directly to Emery and her family. Your contributions assist Emery in receiving medical care as she struggles through the challenges of Sturge-Weber Syndrome.

Custom Ink
All funds raised will be paid directly to Nick Davis for Medical Expenses.
158 items sold
$4,880 raised
150 goal
Thanks to our supporters!
$20
Gildan Ultra Cotton T-shirt
Unisex - White
  • Emery's Army: Sturge-Weber Awareness Fundraiser - unisex shirt design - small
  • Emery's Army: Sturge-Weber Awareness Fundraiser - unisex shirt design - small
Organized by Joy Elise Davis

About this campaign

Emery's rare disease calls for significant medical attention and developmental rehabilitation.Your purchases assists Emery in receiving the best care possible as she struggles through the challenges associated with her rare syndrome. Join Emery's Army.

Emery Grace was born on August 4, 2015. Her parents felt on top of the world as they welcomed the arrival of their new baby girl. After a few hours, they noticed there was something different about their sweetheart. She was born with a large Port Wine Stain, which is a birthmark, on the right side of her face. At the time, her parents did not know the challenges this would bring to Emery's life. Emery has always been a smiley and happy baby. Everything seemed ormal, and i appeare she would live a completely normal life. 

On January 3, 2016, Emery was life flighted to Primary Children's Hospital after having multiple prolonged seizures. She was diagnosed with Sturge-Weber syndrome, a rare condition that is associated with brain atrophy, seizures, strokes, glaucoma, developmental delays and a long list of other lifelong challenges.

Emery's path will be different. There are no sure answers for her future right now, but her parents hope that by providing her with optimal care, answers will be found in the coming months and years. Emery is a happy, sweet irl, who is oved by any. She will have a wonderful life. Join her fight. Join Emery's Army.
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Supporters

Ryan and Tiffany Wilson 1 item
Anonymous 1 item + $75

Please don't send a shirt. Just want to make a donation.

Lisa Davis 13 items
Trost Family 1 item + $25

We're proud to support Emery's Army with love!

Anonymous 1 item
Andra Judd 1 item

I understand, a little, of the emotional roller coaster we go through when our little ones have challenges, whether physical, mental, emotional, etc.. i just know that there is a reason and a purpose and God loves us and wants us to trust in Him.

Anonymous 2 items

I am supporting this campaign, because I like helping others with their needs.

Anonymous 1 item + $100

Denver feels it's of great worth, so do I.

Anonymous 1 item + $150
Anonymous 1 item

Was asked to look at your web site

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