Cian's Kicking Cancer

Cian's Kicking Cancer

About my blog

This blog will be updated by my mummy and daddy to let everyone know how I'm doing and tell you all about the fantastic support that I am receiving from lots of very caring charities.

We are extremely grateful to our family, friends and supporters for fundraising and sending us messages of encouragement.

We also have a dedicated Facebook Page.

Contrasting Theatre Trips

Daily updatePosted by Daddy Case Thu, December 17, 2015 23:16:01

As I mentioned at the end of my last blog, Wednesday night for Cian was with his mum… and as I hoped, both slept as peacefully as a night in hospital can be.

I too had a good night sleep at home.. that may sound a bit obvious, but good sleep is more a luxury now, so I welcome it whenever it happens. It’s also a necessity to ensure that we have the strength to support our whole family.

Mummy Case said that although Cian had a good night sleep, he woke up grumpy due to the pain he was still experiencing. His mood wouldn’t get any better as he was now ‘nil by mouth’ for a few hours in preparation of his impending operation.

Me on the other hand, had it relatively easy getting our other 2 (Dylan and Bethany) ready at home for their school trip.

They haven’t been in school all week, as my emergency recall to hospital early on Monday morning meant that our fragile routine of alternating looking after our well children at home and taking them to school, while the other parent nursed Cian at hospital was sent into disarray. As it is the last week before the Christmas break, their school was sympathetic and allowed the children the time off.

But today was their annual Christmas outing to the New Theatre, Cardiff to see the pantomime; which this year is Aladdin. So we met the school at the Theatre and I even managed to blag a spare ticket to see the performance with the kids.

However, it certainly didn’t escape me that at the same time the curtain was going up, Cian was in a completely different theatre only a mile away; but his experience was far less appealing.

For Lorraine and I it is a priority that we keep things as normal as possible for our other two, as easy as it would be to purely focus on Cian… to the point that we had a slight ‘ticking off’ from a senior doctor as I missed a rather important consultation to ensure that one of us attended their nativity. Something I do not regret for an instant.

All the children from the school (and me) loved the panto and definitely joined in with the audience participation. It’s great seeing children laughing and enjoying themselves, and it has even more significance at the moment.

Not that life on Rainbow Ward is full of children feeling sorry for themselves and despair. Yes, you can hear the sound of seriously ill children vomiting and/or crying resonating in the corridors now and again; but the majority of the time these inspirational kids can often be seen smiling and laughing. Especially when they are visited by special guests!

This afternoon whilst we were all in our respective theatres, The Welsh Guards (in conjunction with Dreams and Wishes) were on the ward distributing Christmas presents. Unfortunately Cian yet again missed the visitors, but they did leave presents on his bed ready to welcome him back from his op.

Cian arrived back to his room with mum just before 5pm. There to greet him, were me; his brother and sister; and his uncle G (my brother Gareth).

He wasn’t in a fantastic mood, but it was considerably better than the last time he woke from General Anaesthetic where he was verging on psychotic. Now Cian is usually a placid kid, and not the kind that commonly throws a tantrum… but when he does, usually through a sense of injustice, it can be quite a challenge to calm him.

So now Cian finally has a Hickman Line installed. For those of you who are curious about the Hickman Line, I have included a photo of Chemo Duck with one surgically implanted.

Cian got his Chemo Duck today. I have to admit, when I heard this thing existed I questioned its value; but after seeing him it makes total sense as a way to portray to children the different aspects of the treatment… and you can’t help but fall in love with the little yellow fellow.

I got to spend a couple of hours with Cian this evening while Uncle G entertained his siblings in the Playroom, before heading back home hopefully to leave mum to have another peaceful night.

Dylan and Bethany will be going into school for the final day of term tomorrow. The whole family will be wearing our Christmas jumpers in support of Text Santa. Although that cause do not appear to aid any of the charities that are assisting us, they are helping others in a similar position.

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