Wednesday, December 31, 2008
Happy new year everyone.
There is not much news from here, which in our opinion is good. Noah is still doing very well, and he is growing, developing and in general very happy.
I'll just post a few highlights:
- There is no news about our home care, or about the house. So for now we have decided to live in The Hague, and see how well it goes. We most likely qualify for a lot of home care, but until this is decided we remain conservative. It looks like we can hope for nursing for 7 nights, 2 days of medical daycare and an unknown number of additional hours. Also some provisions for holidays may be in the packet, but again we are not sure. This is still a mayor worry, but as we cannot afford two mortgages we will stay in The Hague for now. Also it looks like the amount of care and offers for help from neighbours will be enough to manage for now.
We are still looking for a new pram, to enable us to take all his equipment, but still manouvre around in the city, and will fold away for storage in the hallway. Yes we want it all, as usual.
- He is now allowed to breathe on his own, without any machine helping him three times aday for half an hour. This is really great because the little cap to provide him with a tiny bit of extra oxygen is so much smaller then the usual tube, he can move around much better.
- We are trying to give him more solid food, for now this is just training, but he gets a bit of 'pap' with every meal during the day. It is only 10 ml of milk with a bit of babyrice or carrot usually, but he seems to get the hang of it. Also he will be going down to 7 feeds a day,from 8, skipping his three o'clock in the night feed. Good for when he comes home, so we can get some sleep.
The eating is always entertaining:
- Lastly he has grown even further, and is now 68 cm long, and weighs 7.830 kg. Which is almost 27 inch and 17.3 pounds for the more metrically challenged among us :-). This means that he is growing out of stuff, but also starts to fit into some new stuff, including some very fashionable boots!:
Noah wishes you a merry xmas (a bit late, but hey he is still a baby) and a happy new year!
Time for another nap (P.S. Don't try this at home with a baby that breaths through his mouth/nose)
See you all next year,
Louise and Thijs
Friday, December 19, 2008
Make some room in your diary!
Noah is now starting to eat real food. He got bored with only milk, and so we decided to try him on carrots. How else would we keep his hair lovely and red?!
He's not to sure about taking food from the spoon, but he enjoys taking food from fingers and that seems to work ok! He only eats a few mouthfuls but that's a great start.
Both Thijs and myself, Oma, Opa and Auntie Anneke have been busy doing training to take care of Noah and all his breathing apparatus. This means we are able to take care of him without a nurse present when he comes home.
Here is the news we've all been waiting for ... ... Noah is coming home!
Yes, it's true!
We were officially informed yesterday that the hospital is now planning for Noah to come home mid February to the beginning of March. That's only 8 weeks away!
There are lots of things to organise, but the hospital will help us out with a lot of it, we hope! We're also trying to sort out a baby carriage so that Noah can go outside. As you can imagine, we need to take a lot of equipment with us when we take him out. The beautiful pram we bought isn't suitable, so if any of you know anyone who has been hoarding an old fashioned baby carriage up in the attic, the type with the metal tray underneath, tell them to dust it off and get in touch please! We both can't wait to get him home and away from the hospital environment. As soon as we're settled we hope to see you all.
As if this weren't enough of a shock, yesterday the doctor decided to try and see just how far Noah could go. So he took him off all his breathing devices and just gave him some extra oxygen. Noah breathed on his own for 15 mins with no problem! Actually, he was quite upset to go back on the breathing machine, but it's much too much hard work for him to breath all of the time on his own.
However, this does show that it's a possibility for the future. So he now has 15 mins per day of self breathing added into his daily activity in order to strengthen his lungs further.
The doctors and nurses are so amazed at his progress, this has really thrown them into a spin. They are planning another meeting to decide exactly what this means. However Thijs and I just look at Noah and see him giving his cheeky grin and think that this is just typical Noah behaviour. He writes his own rules, go Noah! :)
We also had some people ask whether we received their post, yes we have. We do check regularly on the house and collect the post, so thanks for all the cards we've received, we've put them up around Noah's bed and it's starting to look very festive. The play nurse asked me to decorate the Christmas tree in the IC Unit. She gave me some very tasteful decorations, which I just could not in all conscience use - so I went home and dug out some of my 'unique' baubles and I think the tree looks very festive especially with the traditional Christmas Frog - you'll all want one next year! There was a certain degree of interest from visiting children, so I think it worked out ok.
We're now settled in at the new Ronald McDonald house. It's very modern and only a few steps away from the hospital so that's a good thing.
It's very late so I will just get this posted, Thijs will work on adding the photos later in the day. We are totally not prepared for Christmas and so we need to do a little bit of shopping (mostly to see just how stupidly expensive a new kinderwagen is!!) so the photos may take a little while. I'm thinking of celebrating Christmas in March, I just might be prepared by then!!!!
A few more pictures from the Clini Clowns visiting, and hopefully more news soon!
Tot binnekort!
xx The Drosten juniors
Thursday, December 4, 2008
The Latest Adventures .... plus photos!
As you probably guessed, we have been very busy, but with what?
Well, we'll tell you about that. First of all what we have been doing, and then how Noah has been doing, so feel free to skip to the next paragraph! (And of course pictures are included!)
We have moved to the Ronald McDonald permanently, and have put up our house for sale. Feel free to visit www.funda.nl, (the dutch housing for sale website), and put our address in. We de-cluttered the house, Anneke helped us, plus she took the first few boxes of stuff away to make it look all nice and tidy. We have already had two potential buyers even in this difficult time, so we are very hopeful. It does help that the house is beautiful :-).
The MickyD house is quite nice, here is our view from the window, a few buildings are obscured due to the snow, but it's a nice atmospheric photo!:
And two shots walking home at night. Can you see the heron in the water? The Erasmus hospital is the white building in the background. The colours of the light in the corridor are a representation of the days weather and so it's always new. A very nice piece of art in my opinion (the lights not the iron thing!).
We are not really looking for a new place to live yet, as we don't know how much home care Noah needs and how much financial help to assist with this care we are entitled to. Above this, we can't afford two houses at the same time. We are just starting to investigate how we go about arranging for home care and we are anticipating needing a lot of time to battle through the next layer of forms and bureaucracy.
Louise has had another meeting with her work doctor, who recognized that her stress levels are too high and her fitness levels are too low for going back to work.
Also we have been caring for Noah, who is more interactive and demanding of our time. With that we go on to the stuff you are waiting for - The Noah Update! :)
The last two and a half weeks have had a lot of ups and downs but most of all, a lot of time spent waiting for things to happen.
It started of with Noah's new corset breaking, a replacement was ordered immediately. At the same time Noah was giving a full review. Well, at least all the different specialist were asked to take another look and advise on continuing his care. And so the waiting started......
Without his corset Noah was not able to burp and fart as before, so he was less happy, although not in a terrible way. He was grumpy a lot of the time, and it required a lot of attention from us to settle him down.
A few days after the promised delivery date of his new corset finally arrived, it turned out to be too big! Even though they made it from the same measurements as the first one, it was completely useless. A new one was ordered again.
In the mean time we had spoken with the doctor who promised us that as soon as the corset arrived Noah would be starting on his portable home breathing machine. This is the biggest step forward for him since birth in the process of going home(keep in mind that we need to be trained to use the machine before he actually goes anywhere). You can imagine our disappointment at the delivery of the wrong size.
The new delivery was also delayed, so we had to stare at the fully set up home machine standing idle in the corner for another weekend. But last Tuesday afternoon the corset arrived instead of the Friday morning that was promised, but we were so happy it finally arrived that we didn't complain too loudly. We imagine it must be very busy in the corset making industry this close to the festive season!
Unfortunately ............the nurse qualified for setting up this specific machine was ill, and her replacement was not in till Thursday....... We were now a full two weeks delayed.
We got a stern talk on Wednesday during our regular meeting with the doctor. He warned us that it is very difficult for babies to change breathing machines, and they have to be weaned very slowly. Half an hour a day of using his new machine would be a great first start.
Thursday everyone was ready, and a lot of people gathered around his bed. Louise, the doctor and his normal nurse were there, plus the breathing specialist. They were a bit worried, and even put some calming drugs out in case he really wouldn't like his new machine. So the switch was made, and everybody held their breath for a few seconds...
Noah yawned, burped, and farted very loudly before promptly falling asleep! This cleared everyone away from his bed quickly since they had to breath after holding their breath for that long :0). He is actually doing so well that he has just kept going ever since, not even having a break during the night. They have even removed the hospital machine:
We are very very very happy about this big step forward. We should start our training on the use of his machine on Thursday, and then we will be able to see the end of the hospital hopefully in a couple of months.
Other stuff that has happened:
We noticed that Noah was drinking less and less from his bottle, so a specialist was asked to have a look (one of the many from the big review). It took about three weeks for someone to actually show up, but the result is that Noah will start on semi solid food (pap) on Monday. He seems to be getting his teeth, (yes! teeth not just one for our Noah!) so we wanted to try solid food soon anyway. Another nice step in his development!
With all these nice things, it was a bit unfortunate that Noah had another incident last Monday due to the stupidity of the specialist nurse that takes blood. She started without his assigned carer or one of us there. Noah panicked because of the pain and she did not recognize it, or know how to handle it. During an incident he forgets to breathe and starts turning blue......Luckily Louise walked in and called over a nurse to give him more oxygen while she settled him down. While Louise was settling him, his cannula fell out, which brought all of the nurses running. Everything was put back immediately, and with plenty of oxygen Noah recovered very quickly. It was over within a few minutes, but these kinds of things leave us completely drained.
On Wednesday Noah got a fabulous chair, which two of the nurses went and bought for us as we were busy at the hospital looking after him. Thanks ladies! This chair is great as it secures him in place leaving your hands free to interact with him. He loves it, and so do we! Her are two pictures, one with a chair we borrowed from the hospital, and one in his new one!
Thursday he got a new feeding tube, because the old one was leaking. As he always has a lot of wind problems this tube needs to be finely tuned, a thing which would have some serious consequences..... We finally got a full written description of Noah's medical problems and history. We will read this carefully and try to phone or visit my uncle (who is a pediatrician) with all our questions and for translation of medical terms. I will try to update the side bar of the blog to give you a full description, now that I no longer have to rely on my memory!
Sinterklaas visited on Friday, presenting Noah with many presents, and of course pepernoten (this is the dutch version of Santa Claus, who brings seasonal mini cookies as well as gifts).
Despite the picture he seemed to enjoy a softened, soaked pepernoot.
He also brought a vaccination, so Noah is now up to speed on those as well.
Noah needed his feeding tube (sonde) tweaking a bit because he couldn't release air through his sonde, causing him to vomit, and causing a lot of distress. It needs to end in the top of his stomach, so the excess air can easily escape through it otherwise pressure builds up.
Later in the afternoon my parents dropped by, bringing more gifts, a piggy bank shaped like Noahs ark. Absolutely fantastic!
The plastic surgeon was another visitor who came by to fit Noah for a helmet. This helmet will help encourage his head to grow into a more normal shape (he has been in his bed more then normal kids, so the back of his head has gone flat).
Saturday Nonkel and Lia came by, and gave him a book. Since Noah loves reading it was the perfect present!
When Noah fell asleep, we went downstairs for a coffee. When we returned to Noah after their visit we walked in whilst he was having another incident. He had actually turned completely blue - gray, which was incredibly scary. I was there first and managed to make contact with Noah which always helps. It quickly turned out that his feeding tube was still not in the right position, and when Ichanged his position an enormous amount of pressure was relieved from his stomach (usually know as projectile vomiting). The nurse had to breathe for him with one of those balloons that you see in emergency programs and pure oxygen. It took over an hour for his heart rate to drop to normal levels, so we had a big scare that evening. The strangest thing was that once Noah's oxygen levels went up (within minutes) and he got back on his home breathing machine he kept breathing for himself without problems. Tough little man he is!!
Today Tanja and Rob visited, and brought him some lovely new clothes. We will put pictures up of him in his new outfit soon, for you to check them out. Otherwise it was a blessedly uneventful day.
All in all, a long time of waiting, finally lots happening, all in a few days and a big step forward. The scary bits can be explained, and happen when we are not there to calm Noah down, help him burp and fart and generally take care of him. Some nurses know Noah very well, and do the same, but they often have to take care of two or more patients as well as their paperwork. Also nurses unfamiliar with him don't know how sensitive he is to some things, while being very tough in other areas. So that is why it sometimes takes a while for a new update. We spend the time drinking a proper glass of whiskey instead :-).
Thijs and Louise
Thursday, November 20, 2008
Quick update
Hi everyone,
Just a quick update. Noah's breathing has progressed a lot most likely due to the corset we (and the doctors) think. He is now on 18 hours a day of needing only little support, which is a very promising step. As soon as he is on 24 hours of minimal support he can be transferred to a simpler breathing machine, which can be taken home. The transfer, getting used and training process will take a lot of time (months) but it now seems that he can indeed come home in the near future.
T o show you his smile, we had to rely on visitor, Marijke and Frenzey, who have a vast experience of trying to catch running dogs on camera. They managed to get a good shot of the grin :
Also they told us Lilo is doing fine, and send some pictures to proof that Lilo gets the royal treatment, including her own throne!
Of course an afternoon snooze on the couch is also allowed, as part of the royal treatment.
Well, more news soon, because we are busy arranging lots of things for when Noah comes home, but we'll write about that some other time.
Thijs
Wednesday, November 19, 2008
Picture post
After a bit emotional post, now some hard fact and new news! Of course with lots of pictures for the new internet generation, that doesn't like plain old words :-).
First a picture of one of the nurses, going to clean Noah's throat, which crudely described is like vacuum cleaning the little breathing tube. Luckily Noah doesn't mind this much, he is quite relaxed waiting for it to happen.
As you can see here after the cleaning. His tube needs cleaning quite often when he is active, up to every few minutes when he is drinking his bottle (swallowing means movement around the throat, which irritates and releases phlegm). When he sleeps, his tube hardly ever needs cleaning (all though he often needs a lot of cleaning when he wakes up and starts moving).
Not the best picture ever, but Noah refuses to let his smile be captured on camera. Still you can see he looks happy!
To make clear how difficult it is to catch the smile on camera: even when bopping in his chair he still hides it behind a soft toy. Camera shy?
To annoy the nurses we bought a Toy That Makes Noise (TTMN). The TTMN also has flashing lights, lot's of different noises, and a feet operated bit. We feel it may too much, because we have caught nurses playing with the TTMN. They claim they were setting it up for Noah, but we are nor sure if we should believe them. Anyway, for all of you that think these things make great gifts: THEY DON'T. Thank you from the parents :-)
Random picture without much comment. Cute though......
Even for babies, but also for their parents life goes on, and we had the pleasure and honour to be invited to Franks zero st birthday. He is a friend of Noah (well their respective parents are friends anyway), and was also born a bit early. The party was to honour the day that he should have been born, and his successful move home.
As you can see Frank is not impressed by the festivities (he spend a bit of time in the hospital, teaching him to sleep through an absolute racket).
The feast was big (this was a breakfast/brunch party, and the hosts did not dare to put everything on the table for fear of collapsing it)
And a last shot of Franks proud and happy parents.
Now a new development: Noah has a corset (like one of these tellsell programs). Here he is showing of his new, slim figure. It helps a lot with his breathing, allowing him to sleep while only needing the machine for support. Before his breathing frequency would drop too far, but now he can maintain a normal breathing frequency. Of course breathing this way is still exhausting, but he is back up to 3 periods of 4 hours of breathing on his own, with the machine for support.
The corset also seems to help him fart and burp. This may not seem a thing to be happy with, but Noah has had a lot of wind pains, and moving air out his system is, as far as we are concerned, good! (and sometimes smelly).
Anyway, this is Noah showing of his slim new figure in his American cowboy look. You can imagine him yelling 'rawhide' here (still soundless of course). It was actually a yawn, but it was nearly 7, bedtime for little babies anyway!
And as a final one, a personal message from Noah (in true American style):
To visit!
My parents will organize a party sometime for me, but in the meantime don't be shy!
Louise and Thijs
Saturday, November 15, 2008
Inspiring poem
We believe we are blessed to be Noah's parents, and so lucky to have friends and family like you. So when I read this poem, I felt that it expressed perfectly what I believe, that there is a plan and that plan is perfect, we just don't see it all yet.
I hope you will find some comfort from reading this poem and that it's not too mushy! So thanks Peter for sending me this.
You are who you are for a reason....
by Russell Kelfer
You are who you are for a reason.
You're part of an intricate plan.
You're a precious and perfect unique design,
Called God's special woman or man.
You look like you look for a reason.
Our God made no mistake.
He knit you together within the womb.
You're just what He wanted to make.
The parents you had were the ones He chose,
And no matter how you may feel,
They were custom-designed with God's plan in mind,
And they bear the Master's seal.
No, that trauma you faced was not easy.
And God wept that it hurt you so;
But it was allowed to shape your heart
So that into His likeness you'd grow.
You are who you are for a reason,
You've been formed by the Master's rod.
You are who you are, beloved,
Because there is a God!
Friday, November 14, 2008
Pictures
First of all, Noah needed a EEG because the doctors thought that during his incidents he looked a little bit like he had an epileptic attack. It was only a check of a remote possibility, and nothing like that was found, but a great photo moment!
Here is Noah in his gym, working out while his Aunt Anneke is supervising the excercises (out of picture)
Maarten O.L. also dropped by, but all the exercise made Noah to tired to wake up.
And it was also Halloween recently, for which Noah has a fiiting outfit.
Another very fitting outfit. (I won't remember any of this)
Off course plenty of bath times, but one picture will probably do for now.
Opa and Oma also come to visit quite often, so here is Opa with Noah.Well, hope you enjoy, and more post (and maybe even pictures) will follow soon.
Thijs