As I’ve said before and I still stand by this, nobody has a duty to give me a job, if they don’t want to.
I do miss
the freedom to also have a focus, to stive to achieve a goal and getting there.
which comes with having a job.
As much as
I don’t want to admit this, despite taking few sick-days in my time, looking at
the other conditions that come with multiple sclerosis (MS), I understand why
people are unwilling to employ me.
If, like me, you ae a workhorse, you never get use to the pain of not working but you accept, the conditions that come with MS are out of our hands.
When my GP said to me: "I have to sign you off from work", I hated her for saying these words to me, but within five minutes of her saying this, I knew she was right.
Sadly I still keep applying for jobs, hoping that someone will give me a chance.
I also accept
employing a person who is dealing with::
Depression
Memory
issues
Vision problems
Losing my
ability to write
Fatigue
Motability
issues
Numbness
Loss of
balance (wheelchair included)
Dizziness
Spasms
Cognitive
issues
Anxiety
Tremors
Pain
Bladder
issues
Bowel
problems
Motor skills
Work meant
I had skills that I’d practiced long and hard to perfection. To lose these
skills and abilities, because of my disability, that I wouldn’t have chosen to
have, and it's still gut-wrenching.
I’ve learnt
how to speak again, using exaggerated articulation but I can’t write or
audio/touch type.
I still apply
for jobs that are for a data entry person but they won’t contact me again,
despite these jobs being seated jobs, which is suited to my needs.
Remember
this, to all people with a long-term health issue:
YOU ARE
HERE BECAUSE YOU HAVE EVERY RIGHT TO BE HERE!
Light and
Peace
Andria

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