18 DAYS TO DBS
Well,
now I know what I have its time to deal with it……………………..isn’t it?
No it wasn’t
not in my case. I was offered initial medication but I refused it saying can we
talk again in 6 months. This was accepted by my Doctor and consultant, I think
they knew I was in denial and prescription drugs to be taken every day would be
acceptance and I wasn’t ready for this!
I was
working for myself at this point in my career/life. I started my little
business about 1 year ago installing bathrooms and kitchens and basic
construction. It was something I had always loved, working with my hands.
How
ironic, I am in a happy place enjoying this new career working with my hands
and I am given a condition that sooner rather than later proves impossible for
me to do this work I enjoy so much!!
I had
made this change in my life after working in senior management jobs for about
15 years. Although I had enjoyed my career there was always stress and I did
wonder if this had anything to do with my condition? I still don’t know!
Anyhow,
moving on I continued to work but it was becoming more difficult to carry out
simple tasks at certain times. There was lots of examples where I struggled but
one that was becoming impossible was turning a screwdriver!
I only
managed until about August 2005, 6 months after being diagnosed and I had to
accept I needed the medication to try and control my symptoms.
My life
on medication EVERY day had begun
I
managed to work for another 2 years or so but eventually it got to the point
where I became totally frustrated with myself and frankly to slow to give the
customer a completed job in a reasonable time.
So what
now? If I can’t work what do I do? I had never been out of work for more than a
month since I was 16! You want to believe you’re a decent person, worked all
your life, paid your dues surely it was going to be a straight forward process?
Little
did I know at this time but I was about to embark on the hardest 12 months of
my life fighting the system for basic entitlement.
If it hadn’t
been for Parkinson’s UK and a man called John Bucknall (Benefits Advisor) I
think I would have given up!!
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