Thursday, November 26, 2009
We made it.
Wednesday, November 25, 2009
T minus 1 day
Saturday, November 21, 2009
Just a quick note
Friday, November 20, 2009
To the support crew
Tuesday, November 17, 2009
The end is in sight.
Friday, November 13, 2009
Constantly moving goal posts.
Wednesday, November 11, 2009
Blue, Brown, Green or Hazel?
Saturday, November 7, 2009
The family has landed.
A lucky few were able to come down to the Hospital afterwards and see Sophie, she was due for a feed anyway and woke up for it. We got some photos of the oldest and youngest of the Greenwood cousins, that is to say of Rach and Soph together, which was cool. Sophie put on a display of smiles and general gorgeousness that we were all proud of, she doesn't have to try hard to be gorgeous though :)
Thursday, November 5, 2009
The Doldrums
Tuesday, November 3, 2009
Mummys a silly clogs
Sunday, November 1, 2009
Bye Nikarhn.
My diatribe on the philosophy of procreation.
Saturday, October 31, 2009
Milestones.
Wednesday, October 28, 2009
The Good, the Bad, and the Grizzley.
I had one of those epiphany moments last night where I stopped, looked at what I was doing and thought “what the hell”. I was doing something that would not be unusual for me with one huge exception. I had just spent about 20 minutes unwrapping, reading instructions, plugging in and figuring out how to use a new gadget. Now don’t get me wrong, this is something I quite enjoy doing, and having actually read the instructions before starting this time I had done quite well and was feeling rather proud of myself. The epiphany came when I looked at the assembled device in my hand: A BREAST PUMP. OMG.
If you weren’t able to gather it from the last post, Sophie is now in a cot and holding her temperature well and Deb has moved into the Neonatal unit. Momentous events (suck suck suck on the dummy in the background). She got weighed again this morning (they all get weighed every Monday, Wednesday and Friday) and had put on 65g since Monday, making her 80g up on her birth weight. Baby steps for a baby girl.
With the good things that come with getting a little closer to normality come the bad. Believe it or not it has been some 2 hours since I started writing this, multiple interruptions you see. I don’t mind being interrupted, especially when it is to do something like bath the baby (which we did do, amongst a myriad other things) but now she is unsettled and grizzly and we can’t figure out why. This is very frustrating, you know there must be something wrong and you want to put it right for them, the fact is that if you knew what is was it would probably be quite easily remedied, but you don’t know what it is so you can’t fix it. Then they cry some more, your stress levels go up, they can read this in you and it only feeds their upset and so leads to more crying, a vicious circle of the worst sort. I know this is nothing new to all you parents out there, but it probably amuses you to hear someone else going through it.
Classic Facials
Well, she is getting a bit more settled now so probably time to settle ourselves too. Until next time, Sayonara, Ma Salaama and Au Revoir.
Tuesday, October 27, 2009
And in late breaking News...
Yes thats right Jim, none other than Sophie Greenwood herself has made the astounding move or leaving her incubator, the so called "plasticave" for the greener pastures of a cot. Reactions have been mixed, whilst young Sophie did not have much to say on the matter herself opinions of the main two witnesses to the event, parents Chris and Debra were ecstatic.
When questioned on the matter her mother Debra had this to say "Shes been building up to it for her whole life, it has always been a goal for her and she has been single minded in her determination to achieve it" and her Father Chris siad "I've always known she was going to make it this far, she was never fully comfortable with the plasticave, we are very proud of her"
In this TV blog exclusive Jim we have been able to obtain this rare footage of the event:
Notice how Miss Greenwood shows some dislike for her new surroundings vocalising her distress just as Dad notes how happy she is looking.
And in realted News we have it from reliable sources that Debra Greenwood has been moved into a room in the Neonatal unit itself. It is understood that she has been Lobbying for this move for quite some time and it feeling quite vindicated that unit government has seen fit to acquiesce to her demands. This change in arrangements is going to mean some considerable gains in efficiency can be made, reducing the so called "milk miles" that Sophies milk has to travel to the milk storage and distribution facility. "enough can't be said for the convenience factor" Mrs Greenwood said and "to be right next to Sophie and to be able to wheel her down to my room is just magic". Husband and Father Chris is also said to have been over the moon at the move, and unconfirmed reports suggest that he too will soon be able to stay in this room.
Coming to you live from TBH NNU, this is Reporty Dude Makamanameup for TV blog signing off.
Sunday, October 25, 2009
Can you imagine a better birthday present?
- Maintaining her core body temperature out of the incubator. They have been gradually reducing the temperature in her incubator and will continue to do so until it reaches room temp, about 24^C in the NNU. She is currently at 26^C having started at up around 35. The nurse tonight said she may well achieve this and therefore be out of the incubator by tomorrow. Wicked.
- Getting off the monitor. She still has the pulse oximeter attached, thats the one on her foot to measure her O2 saturation. We can remove it whenever we want at the moment but she still needs it when she is in the incubator. I don't know what the criteria is for having this removed but I suspect it will come off when she comes out of the incubator, so maybe tomorrow for that one too.
- Keeping up her feeds, pushing them back to 3 hourly instead of 2 hourly and putting on weight. As described above this is all important and a gradual process.
Saturday, October 24, 2009
It was a morning like any other....
Friday, October 23, 2009
Role reversals
Thursday, October 22, 2009
To bath, that is the answer.

We covered out her privates to preserve her dignity a little bit :)
A bit more on Deb, as mentioned in the first post in this blog one of the symptoms of her pre-eclampsia was foot swelling. Paradoxically her level of swelling went up after the birth and was causeing her a bit of pain, despite my foot rubbing efforts. This was something to be expected apparantly, although we weren't warned about it and it can take up to 6 weeks for it to correct itself. Not my Deb though, just over 1 week and now her legs are coming back to normal, Yay.
Deb has come home for one night tonight, will do her good to get out of the hospital for a while although she has found it hard to leave I think it is good for her to come home now while she can, because when Sophie gets on the breast she won't be able to. She was given a breast pump to take home with her, great that they should supply her one but wait till you see it, it really must be circa 1950! It weighs in at about 20 kilos and is a VERY solid piece of engineering, we were a little bit disappointed with it at first but now that it is home and set up and we don't have to move it around it is actually quite good, not too noisy and does the job well. I bet the light little plastic ones she has been using up until now will not be working in 60 years time.
Thank goodness Debs friend Lorraine has been very generous and donated us heaps of baby stuff, including a small portable breast pump, so if you read this, thanks heaps Lorraine.
And now for the main act, todays cutesy pic and vid. The picture is of her in her first clothes, and in the video she got the hiccups, which was just a delight and so we just had to video it.
Wednesday, October 21, 2009
The Marsupials will show us the way.
Here she is again, doing the "Dr Evil" post naso gastric tube insertion.
They moved the goalposts on her a bit today, they decided she would need to get up to 26ml per 2 hours not 21, but not to worry she is up to 23 and going strong. We have also been able to get her up wrapped in a blanket like you would any other newborn and hold her while she is having one of her ever more frequent wakefull periods. We seem to be falling into a bit of a pattern whereby she can be got up, changed, fed and have a cuddle every second or so feeding, so every 4 hours or so, it just depends on wether she wakes up enough to make it worth having a cuddle and to interact with her. Something that I havn't mentioned as of yet is that she really does sleep a lot, and I mean probably 22 hours out of the day, but that is also getting better.
She has also been moved into a smaller side room, still in her incubator but out of the main hustle and bustle of the main area. She was moved to make room for possible newcomers and there was indeed a few new additions to the neonatal community today, they really seem to be coming and going all the time.
Grandma Judy and cousin Gabi came and visited, they timed it well and she was having a feed and nappy change, during which she woke up, wide awake and so Grandma and Gabi got to have a hold. Both of them seemed to be delighted with her, and how could you not be? Gabi got all clucky which was nice, Gabi if you are reading this I think that you will be a wonderfull mother someday.
Another vid of her having awake time.
I mentioned Kangaroo care yesterday and promised I would explain so here it is. Kangaroo care is another way of saying skin to skin contact, this is something that is encouraged in all newborns and to put it simply involves having the baby naked on your bare chest (nappy on), and it is not only for Mums although Mum is probably best because she has the milk factories. There has been a lot of studies done on this and they show that the babys generally do better when they get plenty of this one on one contact. The name presumably comes from the fact that marsupials, kangaroos included rear their young (which are born earlier than in other species) in this way. We saw Sophie benefit from this directly, in the first couple of days when she was having brady's and apnoeas the frequency of these noticably decreased when she was having a skin to skin cuddle, there was just enough stimulation from listening to our hearts beat, feeling us breath in and out and making the thousand tiny adjustments we make all the time without knowing to keep her from slipping into the bradys and apnoeas. It also helps with bonding and I can personally atest to that: The moment when she first was gently placed on my chest, her beating heart so close to my own and she lifted her head up looked around and then seemingly found me and stared into my eyes was a life changing moment, it will be etched onto my brain forever and will be treasured with my most precious memories.

Deb having "roo" time.
I realised today that I had fallen into a sense of security about Sophies progress, and to be sure she IS making good progress, better than could have been hoped for but on relfection she is still not out of the woods yet. She has a clear path to follow and Deb and I (and the good staff at the NNU) are holding a hand each to guide her but in the end she will have to be the one to find her way out.
Deb is doing great too, making another one of her super human recoveries. She refuses pain releif where others would be crying for more and stoically bears the sleeplessness. She amazes me every day and will probably continue to do so, although I should probably tell her so more often.
I funny thing happened today: I was sitting today holding Sophie, all was quiet and she was very alert and looking around when one of the other babys started crying. I looked at her and I could have sworn she did a huge eye roll, it wasn't of course but it was damn good impression of one and really made me laugh.
Tommorow... To bath or not to bath, that is the question.
Meal times will never be this easy again.
I havn't explained about feeding so let me try. Sophies suck and swallow reflex has not yet developed, therefore she cannot feed directly from the breast. This has two major flow on effects, the first is that she needs to have a tiny tube inserted into her stomach through her nose and down her throat so that her milk can be administered directly into her stomach. The second is that Deb has to express her milk.
Now expressing milk doesn't sound all that onerous but it has been responsible for us getting a taste of the sleepless nights associated with being new parents. Deb having had a caesarian was not in a position to be constantly getting up and down to get the breast pumping equipment so that duty fell to me (I had been sleeping in with Deb all along anyway). So, every 3 hours and every 4 at night the ritual is: going down to the "milk room" getting the pump, removing the gear from the Milton (sterilising stuff) and asembling it, bringing it back to Deb, waiting while she does the deed, 10 to 30 minutes depending, storing the product, disasembling the gear, cleaning the gear and replacing it in milton, returning the pump and if at night, going back to bed.
What a polava.
I was going to get a Fonterra sticker and put it on my back but didn't think that it would go down well with the other Mums :) I kept this up until she was able to move about and now she is doing all this herself losing sleep while I at least get to sleep through the night, that is if I can get the two of them out of my head for long enough to get to sleep.
Back to Sophie.
So the idea was to start her off on 1ml of milk (colostrum at first) every 3 hours and build our way up to 21ml every 2 hours. In this way her drip can slowly be tapered off until she is up to the 21ml, then they can remove it and we will be able to bath her!
Baby steps
The feeding process is quite interesting, first the attach a syringe to the feeding tube and suck all the air out, burping will never be so easy again. They then attach a syringe with the appropriate amount of breast milk in, remove the plunger and the milk syphons into her stomach under gravity. It takes 1 or two minutes. Meal times will never be so easy again. We are learing to do this ourselves but the Nurses still take care of the timings and amounts. So she is slowly being increased in this manner as she can tolerate it and I am pleased to say she is tolerating it well and will be up to 21ml in no time.
We had a timely reminder of just how well she is doing compared to her peers today, she had a new neighbour turn up today. A wee boy of the same gestational age as Sophie, poor little chap had to have the CPAP machine put on and so is pinioned on his back with this great hulking tubes stuffed up his nose forcing air down him. It is a well studied and accepted fact that pre-term girls do better than boys. When we asked our specialist why he just said that Men have always thought they were the stronger sex but they were wrong, that one is for all your ladys out there :)
Now for the real treat of this post. When I arrived today Sophie had been sleeping for quite a while and we wanted to get her up for a kangaroo care session, will explain about those in tommorows post. So we turned her over to change her nappy (and yes she wees and poos like any other baby) and by the time we had finshed with that she was WIDE awake, looking around and genearlly just being a gorgeous little girl, and I took some video, so here you go.
Isn’t she just a pet? My heart just bursts with pride every time I see this.
One other thing of note happened today, she had the dreaded IV line changed from one arm to the other. Strangely enough she tolerated the procedure well, thanks in large part I believe to the pain relief she received. This is another of those “wow that is really interesting” moments, the pain relief consisted of nothing more than sucrose solution, sugar water dripped into her mouth, and it really worked! The trouble started when they came to remove the old one which had been fastened with a splint and sticky (really sticky) tape, she had a fair paddy man, worked herself up into a real state, which we had never seen before, cried her little heart out poor thing, all good exercise for her lungs I suppose and she slept really well after that.
It is one year to the day tommorow (the 22nd) that Sarah was born and died. It is going to be a rough day I think, we plan to spend quite a bit of time down at the cemetery but the weather might put the Kaibosh on that. In any case we will be with her in our hearts, Sophie too, even if she doesn't know it yet. If you want to do something for us and her just take a moment to remember her if you met her, if not just know that she existed and that she was a person and that she was loved, the fact that she exists in your minds and hearts, if even for the few moments while you read this gives me solace....... Thanks.
Perhaps I should have called this post "tears on the keyboard"
Let the roller coaster continue.
Tuesday, October 20, 2009
Fancy a morning Latte?
As mentioned earlier Sophies biggest problem was to be her breathing, her lungs were formed enough to breath but this was not the end of the matter. It is common in premmies this age to have what they call "Brady's" which is an episode if bradycardia where her heart rate would slow down from about 130 beats per minute to around 80. Associated with this is Apnoea's where her respiratory rate would slow right down, the problem here being that she is just so small and her muscles so weak that she just gets tired and forgets to breathe!
As you can imagine when this first happened we fair panicked. All manner of alarms and flashing lights go off and you can see her heart rate and respirations fall and after a small lag period her oxygen saturation as well. The only positive being that all that is needed to get her out of it was a bit of stimulation, a pat on the back, pick her up and put her down, just taking her blanket off was usually enough. We can be thankfull for that as some babys her age need CPAP (continuous positive airways pressure) where air is blown into there lungs or even in some situations intubation and ventilation!
Day one she did not do too many of these, but on day two the frequency increased slightly. Not too uncommon we were told but could also be an early sign of infection, this turned out to be the case but only a little skin infection in her goin area and a zit on her neck! Easily cleared up with a little topical anibacterial cream.
The frequency of these Brady's and Apnoea's has slowly decreased to where today she has only had a few, which as you can imagine we are pretty stoked about.
There is a stimulant they can use to reduce the amount of apnoeas and brady's that neonates have...... None other than good ol Caffiene! The first time I came in and they told me they had given her some I looked at the nurse indredulously, then looked at Sophie WIDE awake, eyes open and moving around (she doesn't do much of that yet) and thought well, it works for us why not them? The real funny bit is when they had her IV line temporarily removed they added some caffiene to her milk! Latte anyone? LOL
I will cover feeding, breast milk and how she gets her nutrition later.
I am going to fast forward a bit here to the later events of the day she was born (thurs the 15th) and come back to Sophies ongoing health issues a bit later.
That night just happened to be the SANDS group (Stillbirth And Neonatal Death Support) candle lighting ceremony, which is a small ceremony where you can go along and light a candle to remember your lost little ones. We had planned to go to remember Sarah and Deb wasn't going to let a small thing like major abdominal surgery stop her! So we bundled her into a wheel chair and wheeled her down to the chappel where the ceremony was conveniently being held and lit our candles for Sarah. What a trooper. If our tear ducts hadn't been pushed to the extreme allready that day then they were after that. The ceremony was lovely and I think it did us good to have some emotional release, we have been feeling fragile about Sarah for a while now as her anniversary is coming up and the investigation into her death is still ongoing.
Can you imagine more of a rollercoaster of a day than that? Extremes of emotion, first anxiousness and worry, then elation and joy, right back to grief and sorrow. We felt like ping pong balls on the table tennis game of life, and it was one of those crazy chinese olympians playing for gold!