My own Christmas miracle....

That's how I'll remember this December. How else can one explain the rapid recovery my girl has made from this illness? Despite the predictions of the doctors, the way the illness was progressing, and the standard recovery time for HUS, we are going home weeks ahead of schedule. Prayer works. I had asked that everyone pray that we make it home by Christmas, and the doctors are now telling us that not only will we be home for Christmas, we should be going home on Saturday or Sunday! Amazing! Praises fill my heart.

Joyful, joyful, we adore Thee, God of glory, Lord of love;
Hearts unfold like flowers before Thee, opening to the sun above.
Melt the clouds of sin and sadness; drive the dark of doubt away;
Giver of immortal gladness, fill us with the light of day!

How can I help but sing when I look at my little girl's face, no longer constantly strained in pain or ghostly white? Praise the Lord for the great things He has done!

(Our happy Willow Grace tonight after receiving a holiday Barbie from our dear friend, Leslie)

Tomorrow, Willow Grace will have surgery some time in the morning to have the catheter removed from her tummy. Depending on how everything goes, she may or may not need to have a blood transfusion. We're praying that all goes well and no transfusion is needed. After that, we'll watch her blood levels and her nutrition, and those two things will determine when she will be released to go home. Home. That sounds so good and so hopeful to me now.

The last two days have been so joyful. Constant good news and lots of play time with my sweet girl. She's actually been out of bed singing, dancing, and walking around. While she's still be a bit wobbly on her feet, she has still managed to make the most of what energy she does have. We also finally gained clearance today to be taken off of "no contact" when her final culture came back declaring her free of e. coli! Before that came through, however, the physical therapist gained special permission for her to leave the room. The condition was that she had to suited up in a special yellow gown and hospital gloves. We told her that we needed to put her princess gloves on and a special Belle gown, and she was more than happy to comply!

(Willow Grace in the hospital playroom in her "princess" gown and gloves)

I know I've said this dozens of times here and in emails and on Facebook, but thank you so much for all your prayers. We appreciate them more than I can ever express. And I now ask that you continue to pray for us. Pray us home. And pray for Willow Grace during her surgery tomorrow, for the rest of her recovery here and at home, for our transition back to "normal" life after being in the hospital for so long.