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Back To Theatre

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Hi everyone

So after a steady few weeks with Oliver gaining weight and overcoming his infection we didn’t get this week off to a great start!

It’s half term here so we left Oliver in the excellent hands of Ward 28 to visit Paul’s nan in Bournemouth for one night.   On Monday as we were heading home, we got a call to say Oliver had spiked a temperature due to an infection and the line needed to be removed.  Oliver had become poorly quite quickly and needed oxygen.  By night Oliver had been to theatre before going to intensive care to recover.

On Tuesday we rushed to see Oliver who was unsurprisingly a bit grumpy but thankfully back on Ward 28.  Our gorgeous boy had taken a big step back with nasal prongs and a cannula in his foot, as well as being monitored for oxygen saturation. His feeds had been stopped so he was very hungry with no TPN or milk to satisfy him.  Luckily the doctor agreed to resume his feeds, and Oliver was instantly content!

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A slightly grumpy boy fighting the germs

Oliver is now off the oxygen and has a scalp cannula as his foot cannula didn’t last. He is much brighter in himself and we now need to wait until early next week until the doctors are sure the infection has cleared before he goes back to theatre for his third line.

Oliver is very lucky to be visited every morning by the fabulous play specialist Emma.  Emma visits Oliver before we arrive in the morning and is keeping a lovely diary of Oliver and his playtime adventures.   She even managed to capture Oliver smiling at his toys this morning. ..

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First ever smile on camera

Today we had our first big meeting where we met with his Consultant, the Ward Sister, Dietician, Pharmacist and Surgical Registrar to discuss Oliver and the overall plan.   It was really helpful to be able to speak to everyone at the same time and although the end is not yet in sight, we do know the rough plan of action…the main obstacle to overcome being whether Oliver’s small intestine does stretch with the current procedure and if it doesn’t what happens next.
Our next steps are to start to learn how to put up his TPN so this will mean regular overnight stays with Oliver which will be a juggling act but means we’ll be ready to bring our boy home when the time is right!

The good news is that once Oliver has his new line his TPN will resume as it was with 7 hours break….so the plan to bring him home on Christmas Day is still possible.

As always thanks to everyone who has read and shared my blog. 

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Piling On The Ounces

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Hey everybody!

First of all, hello to all my new followers!  My blog has now had over 6000 views and I’ve got fans as far away as Australia and America!

I’ve had a good week and now weigh 10lbs 5oz!  The doctors and nurses keep saying how well I look and everyone loves my chubby cheeks!
My feeds have gone up to 8ml every 3 hours which I love!  Even if I’m having a sleepy day I still wake up enough to guzzle my milk!

On Monday the surgeons came to see me and put a catheter in my stoma.  This is a long tube with a bung in the end and they keep the bung in for 4 hours and then take it out for 2 hours to try and stretch my intestines.  I don’t mind it and hopefully it will work as I really want to see what this “home” place is like.  It sounds nice!

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Me and my big sis!

I’ve had lots of fun this week and Emma the play specialist has been to play with me lots.  She brought me a special chair called a Bumbo and I’ve been sitting in there and trying to hold my head up.  She sings lots of songs with me too and takes lots of photos for my special diary.

Mummy and Daddy have learnt how to lock my line when my TPN finishes so they have done this every day this week and that’s meant I could have a little walk round the ward with them.   I love being out of my room, there’s so much to look at and lots of bright lights!
I had another bath this week and Mummy put lots of nice bubbles in and Daddy held me in the water.   I splashed around a bit and decided baths aren’t actually too bad!

My big sister Ella had a day off school yesterday so she came to see me and gave me lots of cuddles and played with me.  When my TPN finished we all went down
to the café for lunch but because I couldn’t have anything I had a little sleep instead!

I know when my Mummy and Daddy are with me and I love seeing them.  I can almost smile and reckon I’ll get it sussed very soon!  In the meantime it’s really funny watching Mummy and Daddy do silly things to try and get me to smile!

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Having a nice cuddle with Mummy

My Mummy, Daddy and Ella are coming to see me in a little while so I better have a little sleep before they get here.

Speak to you soon.

Love

Oliver
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Size Does Matter

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Oliver has been doing really well lately and is now a whopping 9lb 11oz.  He is still on antibiotics from his infection but they are due to be discontinued this Friday so we have our fingers crossed that his infection has gone.

The little dude is spending more time awake now and is really alert.   It’s lovely that he now responds to our voices and looks right at us and we can interact with him a bit more.  He’s still not too keen on his baths but we put him directly in the water the other day and he didn’t seem to mind it as much as when he’s in his bath seat. Rather than screaming he looked quite puzzled!

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Oliver’s usual reaction to bath time!

His TPN has been able to be brought forward so his 4 hour TPN break starts at 2.30 pm and that meant we were able to take him down to Starbucks at the hospital restaurant today.  It’s only the third time we’ve managed to take him off the ward so it’s still a real treat for us.  Oliver even woke up to have a little look around!

Oliver also had an ultrasound on his liver last week which has shown that his liver damage has not got any worse and his jaundice levels are improving.

The bad news, however, is that his barium study has shown that he has less bowel than the surgeons had thought.  He has about 20-25 cm left which is 25% of what he should have.  To manage a “normal” life he needs at least 50cm so the next steps are for the surgeons to carry out a procedure to block the end of his stoma to try and stretch the intestine.  This will involve another general anaesthetic and the process is likely to make Oliver unwell.  This will take 6-8 weeks and when they carry out the reversal the surgeon is planning on cutting out a section of bowel and cutting it and sewing it to make a longer piece. We are very fortunate that the surgeon looking after Oliver is very experienced so we know he is in excellent hands!  It’s likely this may postpone Oliver coming home and he will need TPN longer term so we will soon start to train how to manage his TPN at home.

We remain positive that we will finally get our gorgeous boy home one day and in the meantime we need to make the best of the situation…. we can guarantee Oliver will have the best decorated room in the hospital at Christmas!

As always, thank you for reading and following our little hero’s journey.

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Oliver and Daddy in the coffee shop

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Blood Transfusion Number 10

After a week of good progress we’ve had yet another set back, this boy knows how to keep us on our toes!

On Tuesday Oliver’s scalp cannula was removed, his feeds increased to 4ml 2 hourly and his urso (medicine for his jaundice restarted) and he was alert, happy and all looked good!

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Oliver enjoying a nice cuddle with Daddy

On Wednesday we noticed a strange rash on Oliver’s left leg so vitamin K was started, thankfully this hasn’t spread or got any worse.   He was due an eye check up this week but it was decided to postpone this until he’s better.  We had signs Oliver wasn’t himself on Thursday and Friday as he’d been unsettled for the nurses and very sleepy when we visited.  The decision was made yesterday to move Oliver back to Ward 12 for closer observation over the weekend and another antibiotic has been restarted. Whilst all of Oliver’s observations have been good his haemoglobin levels were a little low so he’s now had his tenth blood transfusion!

Oliver has been visited by the physios this week who have been great at suggesting exercises to strengthen his neck and encourage him to face the other way as he tends to favour facing to the left and is getting a wonky head!

We also met another member of the surgical team yesterday and they will be doing a barium study on Oliver, once he is well enough, to see the progress of his gut.  We were given another reality check when he explained that even when the stoma reversal takes place there is no guarantee it will be a success and another stoma may be needed. :-/

At the moment it feels we will never see the day we get to bring our boy home but we’re trying our best to stay upbeat!

On a more positive note we had a meeting with Action Medical Research this week who are funding a study into the causes of NEC at the moment and I will soon be sharing our story with them. Oliver took part in the Dove Study
before he developed NEC and hopefully his results might give some clues to why this terrible disease occurs.

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One gorgeous sleepy boy having some tummy time.

Until next time, keep sharing and following on Twitter @franhjones!

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Back to Ward 28

Hi fans!

Sorry I didn’t update you all last week but I was feeling pretty poorly. I’ve mostly been resting and fighting those germs.

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This is me sleeping on my Mummy’s chest!

I had 4 days on Ward 12 where the nurses could keep a closer eye on me.   They soon realised what a tough little guy I am when after 2 days I took my oxygen nasal prongs out by myself and managed just fine and I moved back to Ward 28 on Saturday night.

Daddy had a shock when he came to see me on Thursday.  Mummy had warned him I was a bit yellow but he decided I looked like a corn fed chicken.  He’s so cheeky….I’ll get my own back when he changes my nappy next!

After 48 hrs with antibiotics locked into my broviac line to try and kill those nasty germs, the doctors tested my line again and it was ok so on Friday night my TPN got restarted.  I have had to have lots of blood tests, which means getting jabbed in the foot, but the doctors are happy that the magic numbers are getting better and I don’t look so yellow either.

I have missed my bottles so much and have been a bit of a diva demanding my dummy. ..a boy’s got to have some pleasure!  Thankfully the doctor said I could start having bottles again today so my Mummy and Daddy gave me 2mls of milk every 2 hours today.  It tasted so good even though it was only a tiny bit.

I still have my silly hat too as I need my cannula for my antibiotics for a few more days yet. The nurses try and wrap me up so I don’t pull at it but I’m quite good at wriggling!

I had my photo taken for the Leicester Mercury too as Mummy is trying to make people aware of how nasty NEC is and for this blog!
http://www.leicestermercury.co.uk/Celebs-help-mum-s-blog-raise-awareness-plight/story-19858592-detail/story.html

That’s it for now as I’ve got to get some rest as my noisy sister is visiting with Mummy and Daddy tomorrow as she’s got a day off school.

Keep following my mummy on Twitter @franhjones and my blog.
If you feel generous please donate via the Donate tab as this will help the NNU ward where the lovely doctors and nurses helped me get better.

Lots of love

Oliver
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Oliver’s new bedroom

Hi everybody

So I hear my blog has had over 700 views now, impressive hey (a little like me!).

On Monday night I moved to my new home on Ward 28 at Leicester Royal.  It’s a children’s ward so it has lots of bigger kids as well as a few babies like me. I’ve got my own room with a big boys cot and I’ve got my toys to make it nice.
My sister will like it here because there’s a TV in my room and a big playroom.  The play specialist is even getting her a card and present for when she visits at the weekend. ..and I thought I was the special one!!

I’m now having all my feeds (4ml 2 hourly) in a bottle so I don’t have to have a silly NG tube up my nose anymore.  Everyone thinks I’m really sleepy but I know when theres a bottle in front of me and quickly make it disappear!

I got to have a nice cuddle with my mummy today but I was a bit too tired to play…I’m saving my energy for when Daddy comes to visit as well tomorrow.

Talk to you all soon.

Oliver. X

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Oliver graduates from NNU

As if being an hour away from Oliver wasn’t bad enough I’ve got a sickness bug so haven’t been able to see Oliver for 2 days so far.  Good job Paul is taking lots of pictures for me although he’s back at work tomorrow so he won’t get a visit. I want to see him so much but need to know I’m not going to pass on my germs!

Oliver was moved from NNU to the children’s ward last night and has a side room because he’s young and in isolation. His favourite nurse Keara got him all ready for his move doing his care, changing his stoma bag and putting a fresh baby gro on and took him to the ward. He now has a full size cot so looks tiny in it.

Oliver now weighs 3kg (6lb 10oz)