Complete your support for #!
Create Your Own Fundraiser Learn More

We Did It! Our Custom Ink Fundraising Campaign Has Closed

Need shirts for your next group event? Create your own custom t shirts.

Interested In Fundraising With Custom T-Shirts? Start Your Own Custom Ink Fundraising Campaign

Andrew Michael's FH Fund

Organized by Tanya Baltazar
Front large extended
Andrew Michael's FH Fund Fundraiser - unisex shirt design - front
Andrew Michael's FH Fund Fundraiser - unisex shirt design - back
Andrew Michael's FH Fund shirt design - zoomed
Andrew Michael's FH Fund Fundraiser - unisex shirt design - front
Andrew Michael's FH Fund Fundraiser - unisex shirt design - back
Andrew Michael's FH Fund shirt design - zoomed
Gildan Ultra Cotton T-shirt

Help us raise money for Andrew's journey with FH!

Custom Ink
All funds raised will go to Tanya Baltazar, the organizer for Andrew Baltazar.
$4,760 raised
203 items sold of
100 goal
Thanks to our supporters!
$25
Gildan Ultra Cotton T-shirt, Unisex - Sports Grey
Gildan Ultra Cotton T-shirt
Unisex - Sports Grey
  • Andrew Michael's FH Fund Fundraiser - unisex shirt design - small
  • Andrew Michael's FH Fund Fundraiser - unisex shirt design - small
Organized by Tanya Baltazar

About this campaign

Andrew Michael will be 2 years old on May 6th. He was recently diagnosed with Fibular Hemimelia after being misdiagnosed with club foot since birth. He will be undergoing surgery at CHOP on June 12, 2014.

Andrew Michael was born on May 6, 2012. He was born with a shorter left leg with three toes, half of a foot and an unstable ankle. We were told early on that he had a complicated case of club foot. He underwent castings as an infant, 8 casts total over two months, and then used several AFO braces to try and straighten his foot. It wasn't until April 2nd that we learned Andrew's true diagnosis. Andrew has a rare disorder called Fibular Hemimelia. This disorder effects the leg(s) and feet of children and causes many issues with walking and daily activities. There are two surgical options to help correct the problem; multiple bone lengthening surgeries or amputation. We have chosen amputation for Andrew's left foot and he will be having surgery soon, on June 12th. He will then wear a prosthetic for the rest of his life.Please pray for Andrew Michael and help us raise awareness for all of the children who are born with FH. It is such a rare disorder with no known cause. Thank you everyone!

Supporters

Anonymous 2 items
Sheila Burns & family 1 item + $50

God Bless Andrew. Lori, you and your family will be in my prayers.

Colleen D 1 item

Prayers & hugs from the Dangell Family

tara settle 1 item
Ellen 1 item

This little boy has been through so much in just 2 short years, yet every time I have seen him, he is happy, smiling, and laughing! He is a trouper and will do just fine! God Bless him and his family.

Aunt Diane & Crystal 1 item

Andrew is a little angel who will face this challenge and come out on top with his contagious smile and pure heart still intact.

Sandi Stegura 1 item
Machado 2 items

To Help

Jane Caffrey 1 item

Hugs from the Caffrey family.

Penetra Fam. 2 items

Comments

Share Why You Support "Andrew Michael's FH Fund"

Loading
Loading Facebook comments…