Parkinson's: Poetry by Jim Sheridan
Guest Post by Jim Sheridan
I believe that there is a need to give a voice to those who have
Parkinson's. Parkinson's is a rare breed, for it not only gives us weird
stammers and tremors but it robs us of our voice. It also disguises our agony
with the Parkinson's mask, which others seem to interpret as "I don't care
about anyone or anything".
One glimmer of hope, one light at the end-of-the-tunnel, is having Parkinson's has made me the best person I have yet to be.
When I was diagnosed, friends and family
said:
"what's up with you?"
"you never did this stuff before"
"you're not acting the same, this
isn't you.".
What were they speaking of?
I hadn't gone to a doctor since I was 12
years old. Now I have a Primary-Care doctor, an Endocrine specialist, a
Neurologist, a Movement Specialist, a Dermatologist, a Podiatrist, a
Rheumatologist , and
all sorts of therapist, dietitians and trainers.
I was scared to DEATH!
I thought I was going to die.
I felt the cold breath of the grim reaper
on the back of my neck.
I was given Parkinson's, Diabetes,
Arthritis and Psoriasis.
I joined every support group that I could
locate.
I have T-shirts that proclaim:
•
"I'm
battling Parkinson's, what super power do you have?,
•
"No
I'm not drunk, no I'm not on drugs I HAVE PARKINSONS"
•
"NO
I AM NOT A ZOMBIE...I HAVE PARKINSONS".
These little things bring the disease out
of the dark, in people's face and start conversations.
When I was told about my condition, I
swore I was going to hide it, I was not going to claim it....then a BOOM! happened
in my head,
and I knew:
I'm going to tell everyone,
I'm not going to go down without a fight.
As
long as there is an ounce of fight in me,
I'm going to embarrass the HELL out of this
disgusting disease.
Yes I changed. Before, I never went anywhere, I never
extended myself to help others,,,,but now like Scrooge, I have time to make up
for.
Parkies,
The other day I was
watching Johnny Cash's last music video Hurt on YouTube.
It shows Johnny going
through the years, happy times, sad times, hard times, successes &
failures
Despair and regrets are a
constant memory.
I was inspired by that
video to write this poem; THE DISEASE.
Sometimes it's hard to
separate.
THE DISEASE
This disease
This disease and me
I can't remember if I can feel
Everything still feels unreal
This disease stole my sense of taste
Food has become such a tragic waste
It wasn't content with just my appetite
It wanted more, and more, everything in sight
It took my sense of smell, in the other hand
Every little joy and pleasure it demands
It took whatever was left of my dignity
Hopelessness abounds, sans the Holy Trinity
I shuffle, I stammer, I fall
In the past I stood firm and tall
In my younger days, I was strong and proud
Disease burst into my life fast and loud
It disrupts, rearranges and ransacks your whole life
It cuts completely through like a knife
Rips everything apart like a train through a hurricane
Leaving you feeling the world's going insane
My disease and I
Have become inseparable
My disease is irreparable
I forget where I begin and where my disease ends
Everything in the end, everything blends
My condition is handed down
I've been given a thorny crown
Made to feel like a circus clown
I've been given a life sentence
No chance of repentance
Behind these bars of steel
My disease and my ordeal
In the cold, dank, dark cage, I fall and kneel
This all seems so unreal
What about my family, what about my wife
They should not suffer, the sentence was mine for life
This disease affects everyone, not just me
Why must others suffer
Why make matters tougher
I bleed red, dark crimson
The disease is Parkinson's
Jim Sheridan
2023
Jim, thanks for sharing. Everyone's experience of PD is different, but even when I listen closely to Nancy, I know I'm not hearing the subtext, the silent language inside that feels many of the things you've expressed. She's not experienced all the things you mentioned, but the fear of them can't be denied. I do think it is funny that you've changed in ways that are unrecognizable to your friends. If you'd told me 10 years ago that Nancy would be an exercise fiend, I would have asked if I could have some of whatever you're drinking...of course, now my heart medicine would forbid me from swallowing it, but that's another story. It's really good for me to read the guest posts along with Nancy's because it gives me deeper insights into PD and the issues of those enduring it. Again, thanks for the poem and sharing your personal journey.
ReplyDeleteI thought I'd signed this with my Google account, but this was Nancy's husband Steve posting.
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