I decided to post some more photos of Ben and me pre and post surgery.

Getting ready for me to go into surgery. A bit nerve-wracking.
My actual sugery apparently only took 1 hour, though I was ‘inside’ for four hours. I don’t remember waiting around that long.

If you look closely, you can see the sticky post it note that accompanied my file: "Patient is deaf". I still find it weird to be described like that.
And here is Ben’s last view of me as I am taken in. I was definitely feeling scared as they wheeled me out, but tried to think positive thoughts – e.g: “Anaesthetist promised I wouldn’t die!” Stuff like that.

Being wheeled out of the pre-op ward, and into surgery
After I got out, and had recovered (to read more about the surgery, click here) - the next morning, Dr Da Cruz came and told me it was time to take off the bandage. I was like “What the …? Now? Don’t I keep it on for like a week or something?” He explained that I didn’t need the bandage, I could keep it off, and just have the gauze covering the wound. So, you can see I am mildly freaking out as he takes it off below:

The bandage comes off in the morning, and I don't really feel comfortable without it!
So, what did I do? When I got home, I asked Ben to wrap another bandage around my head! HAHA!

At home after I made Ben bandage me back up. Thanks Ben
I just couldn’t bring myself to lie down on our couch at home, and let my ear/head touch the pillow. I kept imagining germs and bacteria getting in there. Gah! Yuk!
I mean, deep down, I knew that he was right, the wound was sealed enough with the gauze, but I decided to placate the worry-wart in me, and give myself a bandage for the day – just to make myself feel better.
So, I haven’t been able to wash my hair, and I haven’t been sleeping on my head on that side – but it doesn’t really hurt. It”s more that fear you have of hurting yourself!
And then flowers arrived from my girlfriends – thanks guys!

First day back at home, and the door bell rang, and I got a delivery of flowers from my girlfriends.
So, it’s day 5 after the surgery, and I’ve been up since 4am this morning, as I couldn’t sleep. My neck is hurting a bit, and I can really feel the computer chip thing sitting on my skull now – that is kind of freaky. I didn’t think I’d be so aware of it. Well actually, that’s not entirely true – I can feel it, but I can’t actually tell where it’s sitting.
Ben keeps telling me we should test it by dangling some metal over my head, and seeing if it sticks to my head.
Not funny.
I told him no way, I don’t even want to touch it until I see Dr Da Cruz in a week.
But still he keeps jangling his keys suggestively at my head in the hope that I’ll give it a go, see if the keys stick to my head. Am not quite ready to ‘test’ my magnet yet, and am not even sure it would work – wouldn’t you need another magnet to make it stick? I have no idea, and am not going to experiment!
I may be Robo-Kate, but I am still a scaredy cat.
17 days to go until the switch-on.
July 5, 2009 at 10:59 am
All boys are exactly the same. Considering Mat enjoys hanging things off my glasses, I can only IMAGINE what sort of fun he’d have if I came fully equipped with my own personal computer chip and magnet set-up.
I am still confused by the post-it note considering they won’t even do this surgery unless you are significantly deaf. Presumably it is a reminder for nursing staff and other assistants who may do other surgeries and need reminding? – Abigail
July 5, 2009 at 10:46 pm
Hi Kate
Good to “get to know you” via your great blog. I am one of your Mum’s old nursing friends, galvanized into action by her Luddite comments. I will have her know that I am presently loading up an IPOD. Admittedly this was purchased way back in October and I have only just worked up the courage to do it. Maybe the brave Kate facing surgery spurred me on. Good luck with everything. Cheers Sue Murray from Melbourne
July 6, 2009 at 8:22 am
This blog is fantastic and the photos are excellent! It is great that you are writing it as you go rather than just at the end – it really captures the journey you are on. I am very impressed with Ben watching ‘Sex and the City’ with you (I like your mischievous photo) and doing all that cooking. Has he tried the car keys yet?
Take care. Fiona M.
July 6, 2009 at 1:33 pm
Hi Kate
Great work on the blog – I’m really enjoying following your journey.
Lots of love
Katie
July 6, 2009 at 2:02 pm
Loving your blog Robo-Kate. You’re very brave, not to mention a fab writer. Look forward to catching up very soon for breakkie and some shopping
Or when Fi gets her butt into gear – a Mexican and Sing-Star night!
Lots of love,
Shaz xxx
July 6, 2009 at 11:25 pm
Magnets stick to my implant, and metal things can stick to the other side of my magnet… but things that aren’t magnetic don’t seem to stick to the implant itself.
July 9, 2009 at 4:12 pm
Hi Kate
Great it went well. You do have some things wrong in your blog – or at least this is not my experience. Despite the implant not reaching the centre of the cochlea you will still hear low sounds. I quite clearly hear them and as I understand it everyone else reports it to. The robotic sound is only a symptom of your nerves awakening and rengenerating. This goes away and you will hear pretty much like a normal person at least for speech. Music is not quite as good – at least for songs I don’t know – but probably, in time, those you know will sound as you remember them too. I play the piano again and that’s pretty amazing.
About two months after my implant switch on I received a phone call at work. The receptionist told me the caller was a woman but that s all. My caller asked me if I knew who it was. I said well say a bit more and she said well I haven t talked to you by phone for a long time. That didn t help much because that was everyone in my life. But I was able to say it sounds like Joanne. And it was. Now Joanne is my exhusband s sister in-law and I had only seen her maybe 5 times in 20 years. If I could recognise her voice by phone this tells me that what I hear now must be very close to what I used to hear.
July 10, 2009 at 10:55 am
So good to hear these replies from Felicity and Dan Connell. It looks like a C.I might not be too bad after all! Great to hear some differing reports. There is hope for me yet. 12 days to go.
July 10, 2009 at 10:21 am
Mahahaha. Your bf gives me some ideas. If I get bored, i might go up to your floor and poke your head to see what it feels like :p