This is the amazing journey of our two miracles. John Craig was born on November 30, 2005 at 24 weeks and 5 days gestation. He weighed 1 pound 8 ounces and was 12 inches long. John is a true miracle and an inspiration to all that meet him! Hope Amanda, our perfect little girl, is currently recovering from two brain surgeries to remove a 6cm mass from the center of her brain. Hope represents everything good in this world and she too is an inspiration to all.
For I know the plans I have for you, declares the Lord, plans to prosper you and not to harm you, plans to give you a hope and a future.
Jeremiah 29.11

Monday, September 24, 2012

This Is How We Roll!

Multi-tasking on a Monday!!!!!

We've got the feeding pump going, listening to his Brain Core Therapy, eating breakfast and helping Mommy write her grocery list......all before we head out the door for OT and a full day of school.

We don't mess around:)


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2 comments:

Anonymous said...

Hello, I have been reading your blog for years. You are an awesome mother and have really adorable children. I also have a child with a feeding tube. I'm just curious as to why John still needs to be fed through the tube since he has no issues with eating by mouth ? I hope you don't mind me asking...

Jamie and Jill said...

You can ask me any question you want....I don't mind at all. John still uses his feeding tube because he doesn't eat enough food. Yes, he can eat just fine but he burns soooooo many more calories than the average child because of his CP.