6 Days to DBS – I feel a couple of
Blogs today you lucky people!
Well,
this time next week it will all be over, my operation that is!
Today
has started as it did yesterday, awake at 4.30am again!! At this rate I won’t
need a general anaesthetic next Tuesday, I’ll be that knackered I think I’ll
sleep through the 7 hour operation!
I am
desperately waiting and hoping for the letter from the QE Hospital confirming
everything. I know this is one reason for my sleep deprivation. There is always
a chance with the Neurological Brain surgery team something could happen, as in
priorities and my date gets moved. I really hope not I couldn’t go through this
again!
Anyway
tablets taken at 5am, cups of tea and coffee and fags done and 25 minutes of
off time passed. I’m operating as normal again.
I
mentioned yesterday about taking Paracetamol & Ibuprofen and I said I would
explain why I take these some mornings. Normally I sleep quite well and deep
but Parky does play a nasty role during the night on occasions.
I am
lucky because I sleep through it but we occasionally have a serious fight where
he attacks my limbs and muscles pounding me. To defend this I twist, turn,
tense up and only realise how much he has hurt me when I attempt to get out of
bed and this is when I need the pain killers.
People
with Parky’s will also recognise a night with a continental quilt that feels
like it weighs a ton!
7.15am
Starting to struggle, arm has gone limp and face has gone! Waited until7.30
took tablet. Bad off time 45 minutes before able to move arm comfortably!
I went
on FB and looked to see how yesterday’s blog had been received. There were lots
of likes, shares and comments and a particularly poignant comment that I have
to share.
Jeannette is a lovely lady I used to work with. I knew she was following my blog but when I saw this, I was overwhelmed that my blog had impacted on her like this!
10am Here we go again. Typing away
hand just stopped, tongue and bottom lip
dropped!! So frustrating, time for a drink and a cig. Not that bad 20 minutes off
time.
You may be wondering what I mean
by OFF time. For people with Parky’s and the medical staff, doctors, nurses
etc. OFF time is when the condition is effecting you in whatever way you
suffer, stiffness, numbness, shaking, dyskenesia, freezing etc.
Your ON time is when medication
has kicked in and your feeling okay
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