Life happens while you
are busy making other plans. –John Lennon
Where I’ve
been
Truth was I felt like I was drowning. I had to try to save
myself.
I had to rid myself of my jetsam and flotsam. The blog
seemed a bit of a failure, a waste of time. No one would miss it if the blog weren’t
there.
Still, it was a difficult choice. Writers are told we need a
presence on social media, even before we publish. You know, a ‘platform’ but I
find that is a double-edged sword. Social media is great but it is a time thief
and maybe, even a big waste of time. I’m not sure.
Oh, plenty of writers become successful in part because of
their attention to social media. But time is time. How did I want to spend mine?
When I started the blog, I thought the journey I was on
might help someone else. I like the idea of helping another writer, like me. You
know, some someone dealing with caregiving, illness and trying to be a
successful writer. After all, the
journey of caregiving and illness is universal, right? Throw in trying to have
a little writing success—I was navigating obstacles and pitfalls. Learning. My
mistakes and successes with all three battlefronts—maybe, I could help one
someone else.
I could not deny writing the blog did help one person-me.
That wasn’t a bad thing, but maybe, that time had passed.
Before I began writing my blog, I did look for other blogs
about caregiving and writers, about MPGN and writers, about side effects of
prednisone and writing. I found nothing. I could have used the help, the
experience of someone dealing with those things. So why not? There had to be
others like me. Fighting similar battles. Others living/struggling with chronic
illness, caring for an aging parent, trying to write and have a little success.
Maybe, my blog could help, maybe….
I began the blog. I enjoyed writing it. I blessed my son for
the suggestion and help. I kept at it, despite the small following— until—I
couldn’t help anyone anymore. Because I was floundering. Floundering to find
things to write about. Floundering under the changes in publishing and other
things.
And then some things…the caregiving things suddenly became
impossible to share. Too private, too heart hurting. And that, stymied other
things. It became another battle. I could not find the wherewithal to defend
another front.
So, I stopped.
I missed it. A little less each week. I took the time and
made huge strides with my Work in Progress. I started to feel a bit hopeful
again. My disease was under control, had been for six years. I felt good. Able
to handle the caregiving (the emotion and family drama, not so much), though it
was getting more involved and complicated.
I worked on poetry in small pockets of time, which fed my soul, took
some classes and spent time on fun and family. I felt I’d made the best
decision.
So, Here We
Go Again
Of course, the bottom fell out. My disease flared, which really
took me off my feet, emotionally. Why I don’t know. I was well aware there
would be flare-ups, that I would never be cured, that the disease would progress.
Yet, even knowing that, deep down, I must not have believed it. I must have
thought/wanted that none of that would happen. Not to me. (denial 101, ya
think?)
The one good thing was there were no symptoms. I didn’t feel
sick, just a little tired, but I was caring for an elderly parent, a home,
husband, two cats, a dog, a yard.
The worst part is the cure. I wanted to cry when I saw the
lab results. I did. Dr. directions: Prednisone for six months and another six-month
weaning off period. I wanted to shake my fist, yell at…something.
Dealing with the side effects of prednisone again sent me
into a down ward spiral of depression. Yet, as my Dr. and Husband reminded me, (damn ‘em) it was much better than dialysis. I should be
thankful. And I was. Truly. And frustrated. And angry. I wanted to rail and
rant. (I did) I was
thankful we caught it early. And depressed and angry and sad. So many emotions
flooded me, I couldn’t hold on to a one.
Worse of all, I knew what that medicine would do to my
writing. (and hair, and face, and body)
As if the main line tap has been turned off. Nothing comes.
Nothing. Blank. I can analyze while on prednisone, so you’d think I’d be able
to continue the edits, but I was afraid. The creativity part is so gone and
without it, what could the just analytical part do to my work? And my memory
was shot. How could I keep the threads of a novel together? Could I lose what
is unique about my writing? Would I take a chance of losing the best of my
work? I just couldn’t take that chance.
Of course, about this same time things went a bit south on
the care of my elderly parent front. Stress (or as my Dr. explained, how I
handled stress) exacerbates my disease. This was not good.
(Another ‘side effect’
was how vulnerable I felt, anxious and vulnerable. How much of this was the medicine?
How much was just the return of this illness?
My writing would be derailed. For over a year? Stopping writing
again would kill me. I was depressed enough. I wasn’t as sick this time. We’d
caught it early, so I wasn’t sleeping all day, barely able to function. I had
to keep busy, work at something. Something for myself.
I had to fight—I had to Do something.
I wasn’t sure what. I floundered. I’ve floundered before,
but not like this.
(Finally, I surrendered—so I could fight.)
For the last eight months or so, I’ve been on a journey, fighting
battles. It’s not the same journey I traveled before. I don’t really know what
I’m doing. The battles are different, my response more complicated. I’ve
floundered, and sunk and risen. I’ve failed and railed, crawled up, slipped
down. I’ve learned some stuff. A whole lot of stuff.
I got my fight back.
Sometimes
On good days.
So, now what?
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