Some? A whole shelf-full Over 5 litres I reckon!She is in the second bed on the left as you walk into room four. I have tried to upload some piccies of her onto here but I can't get it to work (I'm a bit of a technophobe)! I think Andrew and Amelia share the same milk fridge too, I saw some bottles labeled up for baby Andrew!
We were the same. My husband reckoned we would have a memorial fridge by the time we left. He kept asking if he should call wiseman dairies to borrow a tanker to deliver it with. I'll tell you though, as they start getting bigger, it is amazing how quickly it gets used up. We took a big cool box with us when we went to get her thinking there was heaps in there but there were only 3 bottles!Some? A whole shelf-full Over 5 litres I reckon!She is in the second bed on the left as you walk into room four. I have tried to upload some piccies of her onto here but I can't get it to work (I'm a bit of a technophobe)! I think Andrew and Amelia share the same milk fridge too, I saw some bottles labeled up for baby Andrew!
Fingers crossed for Millie. At least Alder Hay has a great reputation, is it not one of the best Children's hospitals in the country?The cardiologist is going to be reviewing Millie's PDA, they have administered courses of meds to close it but no joy, The doctors feel that the PDA is holding her back from gaining weight etc, and if the cardiologist agrees then there is a very strong possibility she will be referred to Alder Hay to have the operation to close it. I am terrified about her going under the knife, she is so tiny and delicate. But I am told it's a relatively straight forward procedure. Has the duct in Andrew's heart closed on its own or with meds?
The cardiologist is going to be reviewing Millie's PDA, they have administered courses of meds to close it but no joy, The doctors feel that the PDA is holding her back from gaining weight etc, and if the cardiologist agrees then there is a very strong possibility she will be referred to Alder Hay to have the operation to close it. I am terrified about her going under the knife, she is so tiny and delicate. But I am told it's a relatively straight forward procedure. Has the duct in Andrew's heart closed on its own or with meds?
Andrew sounds like a little fighter and he is growing amazingly well. Sounds like you are in an amazing unit.
These premature babies are amazing. My LO is huge now, she has been through a massive growth spurt, three weeks ago I bought her home at 4lb 10 oz, she is now 8lbs (4 times her birth weight). You watch before you know it, Andrew will be huge and you will wonder where your tiny little tyke went.
Another great first. I remember Abby lying licking it all kitten like. We had her fed through her tube at the same time so she got used to getting a full tummy at the breast. I do remember looking down at her tiny head agains my massive boob and thinking "That must scare the beejeezers out of her!"Well, today Andrew stared at my boob ("What do you expect me to do with that? ) and kissed it a couple of times, but didn't associate it with food. Try again tomorrow, if we manage to get there when he's off Cpap - they're changing him to 12hrs off & 4hrs on.
He's going to have an MR scan next week to get a better look at the site of his cranial (extra-dural) bleed. Hopefully we'll get a better idea from those results as to whether there's any damage.
Sorry, not writing much as not in a chirpy mood today.
Meant to say, I also had my 6wk post-natal appointment and discussion with the consultant who runs the Placenta Clinic here ...
The problems I had with my abnormal bloodflow into the placenta, resulting in Andrew's IUGR and premature delivery, are likely to recur. He doesn't think they'd be as bad a second time, plus they would go for a high level of monitoring (doppler scan @ 11 weeks and take it from there), and insist on screening if appropriate.
He recommends we wait at least a year before trying to give the c/section time to recover, and also to see whether Andrew has any difficulties resulting from his premie birth and cranial bleed. He reckons there would be no problem fertility-wise with waiting, as I fell pregnant so soon this time round.
My OH was there when we were told this, he's keen on a second child, but we haven't actually discussed the consultant's advice yet. My worries would be around needing the higher level of care, having a premie and then baby having a protracted SCBU stay, all whilst having a toddler (Andrew) to take care of.
Got a surprise when I phoned (after a long lie-in) this morning to check on Andrew's progress - he'd still not been put back on Cpap since 6am yesterday morning! That was 28 hours at that point ... 33 hours by the time we left him this afternoon, and still going strong just on his nasal cannula!
And he'd been dressed in a cute babygro with "I love Daddy" all over it.
And they've switched him to a nasal gastric tube - nobody really said why, but I'm hoping it's so that they can start cup-feeding him, and to give him more of a chance to breast-feed! Which I didn't try today, I didn't want to disturb him when he was so many hours off Cpap, I didn't want to stress him out more! Save it for tomorrow.
Oh, and he weighs 1.404kg (3lb 1.5oz) now!