So how has it been since? Thursday was actually the best day
in terms of energy levels / pain rather surprisingly! Friday / Saturday /
Sunday I took painkillers every 4 hours and slept most of the day.
Monday I managed to function a bit more, and stretched the
painkillers to 7 hours between.
Tuesday I had no painkillers till 7pm and no nap in the day J
Wednesday I woke up with a stinking head cold. I nipped to
the doctors just to have a wound check and they took my temperature to be sure
it wasn’t an infection – all fine.
Thursday & Friday
still feeling a bit under the weather – but mostly from the cold I think.
Saturday I felt reasonably OK. Still have a tickly
throat and runny nose, but not been sneezing as much (don’t forget to sneeze
with your mouth open, otherwise I’m told it hurts!!) and no headache.
Today (Sunday) it finally stopped being gale force winds and I felt well enough to go for a walk on the beach. I didn't feel as tired afterwards so I think I am finally heading back to normal - though I've discovered the ear / cut does not like getting cold (!)
However I have had a very very relaxed week. Not been
anywhere, not done anything, just napped, read books, watched CSI and been
lazy. I am surprised how tired I get when I do anything and how much it has taken
out of me. I think in my head I thought I would be back to normal much much
quicker than this!
In terms of the implant – the cut has healed very well –
hardly noticeable now. It is tucked very close to the ear which is nice as its
out the way. It is itchy and the skin around it feels odd – like its not mine or something – a bit
numb.
After surgery what I was not prepared for was the bruising
on my jaw. It was both sides, but mainly on the implant side. I had a massive
bruise and it was sore to touch and to open my mouth wide / chew. That has
pretty much gone now (day 10).
My ear was a bit numb and bruised, the bruising and
tenderness has eased off but it is still hard. The other ear I can bend the top
down and its soft and flexible. The implant side the top is hard and much more
rigid.
My tastebuds were affected a bit – nothing too major, but
sweet things taste odd and my cuppa is slightly not right – but nothing too
major.
The most fascinating bit is the bump on my head where the
implant is – its huge!! I didn't think it would be noticeable from the outside
but it is! Some of that may be swelling I would think, so maybe it will get
smaller.
I didn't have much dizziness but more a feeling of being
light headed or off balance, and a feeling of pressure if I bent down. I'm
careful when I get up or turn corners and am paranoid about banging my head!
The main problem is not being able to sleep on the implant
side. I can’t sleep on my front or back, so I am getting a sore ear / hip /
shoulder from sleeping in the same position, but I'm finally managing to sleep
a bit better as I get used to it.
I didn't wash my hair after 48 hours – I wasn't that brave!
I finally did it on day 6 and it was fine – and felt a lot better for being
clean!!
So – what now? Well I have two weeks left till I leave for
activation – yay! I’ll be back at work for those two, though if I get tired I
might work at home. I've been busy searching for therapy resources to help.
I've downloaded audiobooks for two paperbooks I've been saving to listen to
whilst reading, I've got some word sheets and some listening apps. I’ll try and
do a list to go on here when I get time and add to it with any that are useful.
I've been learning to listen with just my bad ear (which
actually is not that much worse than my good I have discovered!) and keeping up
with my various CI groups / forums /
email lists. I have a couple of wonderful AB mentors – Michele who has been
fab, and Colin who was also implanted at my centre. I know another couple of
people on facebook implanted in my centre, and Nicola in Orkney who was done
there 3 years ago. And then there are my friends from school in varying stages
of CI journey so I am blessed with lots of people for support.
Now its just a case of waiting until switch on – and I’ll
try not to leave it so long to update you after that!!
I've decided I will publish this on a blog. Its good for me
writing it, and I know how much I hunted for and devoured every CI blog I could get. They all helped me
tremendously and I’d like the chance to “pay it forward” and hope that I can
help someone else.
This comment has been removed by the author.
ReplyDelete17 November 2013 20:30
ReplyDeleteThank you for sharing your blog, Ronie!
I TOTALLY understand that invisible middle ground that you describe in your first post or two -- I was born profoundly deaf and have always lived in the hearing world, but I am certainly not hearing and also not Deaf (I don't know ASL either). I just chose bilateral MedEls (both ears) at the same time 6 months ago, and can assure you that the 'sound' at activation and afterwards is both exciting and very strange. This whole journey and what I can "hear" is sometimes quite challenging or frustrating as well as exciting, but everything definitely does get better!! Practice, patience and each mapping all help a lot. I am glad you are blogging!
My blog address is www.silencetosoundblog.blogspot.com.
May I put a link to your blog in the "favorite blogs" list on mine?
Wishing you all the best!
Robin
Hi Robin,
DeleteLovely to hear from you - I've added your blog to my links list and please feel free to add mine to yours. I always find it fascinating reading other people's journey's - especially when from a similar hearing background. I don't think I've come across your blog yet so I will go have a read of it today!
May your journey gradually get less challenging and I look forward to keeping up with your progress :-)
Ronie
Yoohoo! Yes it's me - following you round like a bad penny! ;-) Glad to hear it's all going well for you.
ReplyDelete:-) Think we are doing a bit of mutual hanging out in the same places :-) Hope you are feeling better now and will be thinking of you tomorrow and hope the op goes ahead for you. Look forward to an update as soon as you are able! xx
DeleteFeeling lots better (dunno about the nerves though!) I will go to Southampton tomorrow, tell them about my latest history and how well I feel and will let them decide.
Delete