evie jayne: Results and Surgery Update

Wednesday, June 23, 2010

Results and Surgery Update

Hi Friends!

Got a call yesterday afternoon that Evie's CT Scan is unchanged from her last one, meaning her brain pressure hasn't increased at all... PRAISE GOD!

Got a second call this morning, that they are moving Evie's surgery back to July 16th. That is exactly what I was praying for, since John already has his schedule rearranged to have the 6 days following surgery off. Woo hoo! That gives us 3 weeks and 2 days.

I have had a few other things weighing on my mind this morning, but until I get my house cleaned up and my kids napping they are going to have to wait (:

Love you friends! Thanks for praying!
Linds, Ly & Eve

2 comments:

Misty LambertJune 23, 2010 at 1:31 PM
Praise God... all good news.
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Melissa SwartleyJune 23, 2010 at 7:57 PM
FANTASTIC!!! So happy for you all! I love how you have been adopted into a great group of moms and cute kids too! "Holland" just gets better and better! http://www.our-kids.org/Archives/Holland.html
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Our Story

Hi New Friends!

This is the story of our Evie Jayne... as it unfolds. When I was 20 weeks pregnant with Evie, our second daughter, we were told that she had a lethal form of Osteogenesis Imperfecta. We finished the last 4 months of our pregnancy praying for a miracle, but also planning for Evie's passing. Evie was born on September 19, 2009, and the few minutes to hours we were supposed to have with her have turned into months.

Evie has a bone disease called Hypophosphatasia. She has been on a clinical trial since she was 2 months old, and it is going beautifully so far. She is truly a miracle, healed by our Heavenly Father, blessing our lives one day at a time.

So here is our blog to share her story, our joys, fears, prayer requests, and day to day life with our precious girls.

If you are new, here is a link to the Beginning of our Story.