Showing posts with label caregivers. Show all posts
Showing posts with label caregivers. Show all posts

Friday, May 13, 2011

The Truth Will Out

Four-and-a-half weeks ago,
when a mild headache suddenly exploded into head-clawing pain,
I called 911,
and earned an ambulance trip to the hospital.

It was the third time in my life,
all in less than a week,
that I’d experienced that kind of pain.

Calling 911 on myself,
and the ambulance ride --
those were brand new.

Both the male and female paramedics seemed competent,
and, as far as I could tell, they did all the “right things”.

But of all the medical professionals I’ve encountered in past weeks,
they weren’t exactly the kindest.
They were somewhat brusque,
dismissive of my pain and fear,
and surprisingly oblivious to the comfort it would have been to have a loved one near.

As we rocketed over bumps and potholes,
I lay writhing on that narrow bed
gripping the bedside as tightly as possible with my IV hand.
The first medications they administered did nothing to relieve the pain.
My eyes covered due to extreme light sensitivity,
I could see nothing but darkness.

When we’d started our trip,
I’d called out,
“Is anyone back here with me?”
The male medic told me he was,
but even with the assurance of his presence,
I felt alone and terrified.

A few moments later,
after carefully considering it,
I asked the medic if he would hold my hand.
He responded with some surprise,
“You want me to hold your hand?”

To his credit,
he took two of my fingers –
the only ones not occupied with IV and monitor and clutching the bed --
and grasped them in his glove-tipped ones.
Only for a second, though,
for he soon excused himself.
“I’m just trying to get some paperwork done.”

So I released my reluctant comforter to do his paperwork.

In due time,
he finished his paperwork,
his driving-partner delivered us safely to the hospital,
and they handed me over to the care of Emergency Room staff.

Days later,
when I was safe at home, recovering,
the memory of the hand-holding incident floated up to me.

I’d been in so much pain.
so distraught,
so desperate for comfort!

The memory of the paramedics' dismissive tone makes me ask myself:
how many times have I,
as I teacher,
dismissed a child's emotional needs
because I had to "get paperwork done"?

Now that I’ve returned to the classroom,
that question is with me every day.

At the same time,
the memory of that night brings laughter,
for it hints at something I thought was long-hidden:

Regardless of my claims that I’m an independent, single woman,
despite the fervency of my assurances
that I’m delightedly content with my single state --
I’ll go to extreme measures to have a man hold my hand. :)

-- Reenie

Saturday, February 26, 2011

A Month of Life


I missed my first day of work on February 1. This is February 26, and I’m not well yet. I missed four days of “official” work, two full days of unpaid writing, and several partial days. Even when I’ve been back at work, I haven’t felt like myself.

Earlier this week, a local librarian heard me cough and suggested strongly that I should be home in bed. She wasn’t convinced by my assurance that I’d done my time in bed...and this was much better!

As of today, I see big-time progress. I’m still easily tired, but I only coughed a few times today. Woo hoo! I’m nearly well!

In the meantime, I’ve missed a month of my life.

As I'm sure you've figured out, one can do a lot of things with a month. A few summers ago, for instance, I spent an entire month in Thailand. Trust me on this: a month-long holiday in Thailand is better than a month of sickness.

I’ve been inclined to feel just a little bit sorry for myself. Okay, I'll admit it -- more than just a little.

My pity parties last about two minutes -- when I’m brought up short by the reminder that many people are sick for months...even years. They don’t simply miss out on a month of To Do lists before bouncing back to the usual work or school scene.

These people have to give up their entire “usual scene”, because their illness has no known ending. Or because the treatments required to save them from it, make them too sick to be out in public. Some of them wonder if they'll ever have a To Do list again.

I’d never dare to pretend that, after a mere month-of-slowdown, I can understand what it’s like to have a chronic illness.

But I do want to say this...

Hats off to you who are sick, week after week, month after month, year after year. May God give you courage and strength.

Hats off to you who get horribly sick from your treatments... but keep going for treatments anyway.

Hats off to you who care for a loved one for year-in and year-out... but don’t allow yourself to get bitter about it.

Hats off to you who bear a life-long diagnosis with patience and dignity... and refuse to get mad at God.

My greatest hats off, and my deepest bows, go to you who bear chronic illnesses with no family or friends nearby. May you know the Friend you cannot see, but is always with you. May you know how much He cares about you. And may you know that He’s preparing a much grander life for you on the other side.

This life won’t last forever... but that one will! Now that's worth a WOO HOO!!

-- Reenie