When we first learned of Annie's spina bifida diagnosis, communication with our support groups was one of our top priorities. At that time, John decided to host our own domain to get the word about Annie out. As life has continued on (at a rapid pace), the unwieldiness of having to post on an actual webpage (which I don't know how to do), has hampered our communication through the website.
Today, on the SECOND Annie-versary of Annie's fetal surgery, we are launching a new platform. We'll catch everyone up on the happenings over the last few months, and continue to post new updates here.
Thank for your patience with us! Spoiler alert: Annie is doing tremendously well!! While we don't have any specific/urgent prayer requests, I know that many of you feel invested in her and would like to know how she is doing.
From now on, you'll find us at adventureswithanniecaroline.blogspot.com
I'm going to try and copy over all of the original website to this blog, but in the meantime we'll leave www.anniecaroline.come alone--it just won't receive the updates. Please feel free to share this information with anyone you wish.
We are immeasurably grateful for the mercies that God shows us every day. Two years ago, we had absolutely no idea the little person Annie would become. We could not be more grateful for her spunky little self every day. Sometimes it takes big situations like this one to really bring life into focus. We certainly are thankful for every milestone she conquers and are in awe of her abilities.
Surgery day and our first Annie-versary celebration!
Annie-versary 2015! I had no idea how much I would appreciate seeing a baby's knee pull up like hers does in this picture!
Annie-versary 2015. Her precious back--Jack calls her scar her "boo-boo."
"See, God has come to save me. I will trust in Him and not be afraid. The Lord God is my strength and my song; He has given me victory!" Isaiah 12:2
We love ya'll! Happy Annie-versary!
MK
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