3D

(This is her mouth open, tongue half way out and her little arms around her face)

This was a picture from our last specialist appointment.  I kept saying this is my miracle girl and the Lord continues to bless with that each appointment.  The specialist said we officially HYDROPS FREE!!!!  Then the cardiologist said that the small hole in her heart that he saw, has closed up so we are now VSD FREE!!!!!!  As far as we can tell she still has the hygroma on the back of her head, but because she is getting bigger, it is harder for us to see her neck.  She is a mover and shaker for sure.  Brent was able to feel her move for the first time last week (which he said "is cool and weird!)  He has not been patient enough to feel her again, not that he its take much because she loves to kick as soon as I lay down as night!  It's so sweet!

Thanks so very much for continued prayers for total healing!  It's been hard for me to not let my heart just expect the total miracle.  At the same time I am still guarded that she may have Turners or some other type of chromosome problem.  No matter what happens, I know for sure how loved Avery Grayce is for sure!  Not just by me, or by our families but by so many people.  One of my favorite moments last week was when two sweet kids that I love climbed into my lap and asked to see Avery.  I told them both (they are 2 and 3) that she is not here yet.  They asked for me to open my mouth so they could see if they could find her!  Wish it was that easy.