Today is Wellington anniversary day. It’s just another day for us traveling to the hospital. People always ask us if we go in every day or why we go in every day, well those are really stupid questions. Our daughter is just as important to us as all of our other kids, and while she is still in hospital we will still go in there. What kind of parents would we be if we didn’t go and see her. She is the most important thing in our lives right now and until she is home we will not relax.
I would like to thank all the people that leave comments on the blog, even though I don’t respond I do read them. Support is the biggest thing for us, without everybody’s help we couldn’t do what we do.
Anyway when we arrived today we took another cake in, this was called the poo cake. It was banana though, we thought we better not make a chocolate one! Our little girl had apparently pulled out her ventilator tube last night! They left her to see how she would cope and she has gone straight onto Wellington cpap. She thinks she can just do everything by herself now. She has also started back on her feeds again, and they aren’t slow feeding her like before. At the moment she is on 2ml every 4 hours. But they won’t increase her feeds too much until they know she can cope.
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