Well, we go to McMaster tomorrow for another ultrasound and visit with the high risk doctor. I didn't write anything after last week's appointment as nothing much had changed. They did not do any measurements of the baby so we could not really check on the growth of the baby. They only do measurements every two weeks so hopefully tomorrow's ultrasound will provide more information and hopefully Nathan is continuing to grow.
I have found it really helpful to read other members' blogs. Although it's terrible that so many people are affected by CHD, it is comforting that we are not alone and there are people out there who understand what we are going through.
I am very concerned about how this will affect our daughter Maddison. She is so excited to have a baby brother. I have tried to explain that he will be sick when he is born and will be spending time in the hospital but she is not quite 3 and doesn't understand. I also read on the Lobo's blog that children are not allowed in the NICU at the hospital. This has me worried since I figured Maddison and I would be staying in Toronto a lot while the baby is at Sick Kids but if I can't bring her there with me I don't know what we will do. This will all be scary and confusing to her so I don't want her to feel abandoned by me on top of everything else. It will also be difficult because Mike will have to keep on working through all this. (Besides a few days off here and there.) Well, enough of this. I was just venting some of the things that I'm always worrying about.
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