Monday, April 19, 2010

Do you know why I am so happy?

Because I am out of CICU!
And now in the Step Down Unit. Please join me in praising the Lord!

15 comments:

Barbie said...

Oh what a blessing!! I am so thankful for all of you. :-)

Jeanniemb1 said...

Praise the Lord!!!! That is wonderful! God is so good!

Tami said...

How wonderful!!!!

definintely an answer to prayer:-).

God is good!!

Hugs,
Tam

Football and Fried Rice said...

Yeah!!!!!!! Could John Asher smile any bigger? Darling! And what great news!!

Jennifer and Matt said...

Wonderful news!! And what a happy smile that is on John Asher's face!

Mama Leigh Ann said...

Wooooooo Hooooooo!!!!
Doing the happy dance with y'all!!!!!
Love that smile!!
Leigh Ann

Alison said...

Go John Asher, go! We will miss you, but we will visit you on the floor (so don't even think of trying to come back to see us..we will come to you ;)

Alison

Unknown said...

Congratulations! He has got the biggest smile I think I have ever seen!

Trey and Cheri said...

Thank God for answered prayers! So happy for all of you. John Asher could not be any cuter! Still praying John Asher will be able to participate in baby dedication on Mother's Day.

MamaStew said...

What an answered prayer! That is such wonderful news- the CSU (Cardiac Step-Down Unit) is the final step before hitting the road and getting OUT of Egleston! Congratulations, John Asher! Please be sure to tell all of the CSU staff hi from Cabell :)
Praying your stay in the CSU is a very brief one!
Amy Stewart

Jenna said...

WOO HOO!!!!!! So very, very exciting!!!!! That's awesome! Praise God!

Boy, he just looks os much happier....like he's feeling a ton better!!!!

The Huff's said...

Amen!

McCance said...

Fantastic!!! Praise God!

Everything Beautiful Shay said...

Precious baby and looks so sweet and happy!!! So thankful he is doing well and hoping you all are home very soon!!!
Blessings!

Mei Mei s and Mayhem said...

Just found your blog through the china heart yahoo group.

I loved reading your story and Im so happy to hear your little man is doing much better. We will keep him in our prayers!!

OUr daughter has repaired ToF too. Hers was repaired in China at 15 months old. It sounds like she had many of the same complications. She was in the hospital for a month and her nanny through tears said they really thought she was not going to make it.

We got her 3 1/2 months post surgery. She is doing amazing and we have been home 19 months now!! She has more energy than my other 4 kids put together!! No meds and no restrictions!! She will need a new valve sometime in the next few years but all and all things are going great!!

Look forward to keeping up on your blog!! You have a beautiful family!!

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