If anyone feels inclined to come and say hello at the hospital, please do. Visitors are very welcome. I am trying to get back to work and Mimi is sometimes alone at the hospital. Come and see our beautiful baby. Please bring hugs.
Oh man! I wish I Iived there, I'd be there in a second! I think of you guys often and wish I could give Meems a hug, and see that sweet little baby. Hang in there and give that baby a hug for me....and Mimi too!
I wish I could have stayed longer today, but just wanted to say that Mia is such a beautiful baby. We loved having Jensen and Ellie over this morning - they have the most infectious giggles, ever. Please drop them off anytime you need to!!!
OH...I so wish I lived there, Mimi just know that If I could I would be there in a second, to come visit and give you a big hug and see that sweet little baby of yours. She is so perfect and beautiful. Hang in there, and try to keep your spirits up.
I hat to be so nosey Mimi but, I'm going to ask anyway. =) Do you mind sharing Mia's diagnosis. I've tried searching the blog for it and couldn't find it. I have a dear friend lurking and reading your blog whose daughter has Ivemark's Syndrome. She just completed her staged repair this year. Fontan was the 'final' surgery. Anyway, she keeps saying how similar your stories sound and was wondering what the exact defect was.
Still praying for all of you and the support system God has placed in your lives. Praying for wisdom for MIa's doctors and an endless amount of hope and faith to see you through.
11 comments:
Oh man! I wish I Iived there, I'd be there in a second! I think of you guys often and wish I could give Meems a hug, and see that sweet little baby. Hang in there and give that baby a hug for me....and Mimi too!
I wish I could have stayed longer today, but just wanted to say that Mia is such a beautiful baby. We loved having Jensen and Ellie over this morning - they have the most infectious giggles, ever. Please drop them off anytime you need to!!!
OH...I so wish I lived there, Mimi just know that If I could I would be there in a second, to come visit and give you a big hug and see that sweet little baby of yours. She is so perfect and beautiful. Hang in there, and try to keep your spirits up.
She is beautiful and wonderful. I LOVED visiting last night and seeing her so awake. Thanks for sharing.
We are on our way.
Soon!
You have such a beautiful family. You are amazing! Our prayers are with you.
I will take you up on that invite sometime in september! You won't be in the hospital anymore, but I am going to give you the hug of a lifetime!
I hat to be so nosey Mimi but, I'm going to ask anyway. =) Do you mind sharing Mia's diagnosis. I've tried searching the blog for it and couldn't find it. I have a dear friend lurking and reading your blog whose daughter has Ivemark's Syndrome. She just completed her staged repair this year. Fontan was the 'final' surgery. Anyway, she keeps saying how similar your stories sound and was wondering what the exact defect was.
Still praying for all of you and the support system God has placed in your lives. Praying for wisdom for MIa's doctors and an endless amount of hope and faith to see you through.
www.caringbridge.org/ca/morganfaith
I'm sorry I totally forgot to add to my post what Morgan's specific heart defect is. Hypoplastic Left Heart Syndrome (with some other abnormalities).
Hey, I would love to come by this Thursday! Childrens right?
Monica
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