Visit The Directory - locate and preview unique blogs. click here.

73 Visitors are currently online including logged in users below:

Mister

Article real-time statistics…

  • 501Articles read today:
  • 1742Articles read yesterday:
  • 12193Articles read last week:
  • 1321575Total articles read:

Articles listed by month…

Copyright Infringement…

All materials and articles on this site are protected by copyright per the original author or blog owner and published with their consent.

Any re-blogging or re-publication of this content without the authors permission is illegal and subject to liability and criminal prosecution.

Claire - Day To Day With Parkinsons Disease

Surfacing

If the landscape will not change, then one must change the landscape oneself.

“Do you think you could manage a trip to Montreal to visit Laura?” I asked desperately on Sunday morning when it was clear that the expected weekend caregiver wasn’t going to show. I had plans to skip down to the river with the dogs for a long, refreshing swim on yet another hot, dry day, an activity that has saved me the past few weeks from certain despair, the controlled breathing of a hard swim a welcome, calming exercise. But in this caregiving business, I cannot count on anything and must be ready to scrap my plans at a moment’s notice.

Michael was still seated at the table, his breakfast dishes emptied and scattered around him. His response to my question was to fall instantly asleep. Over the years I have learned to decipher the oddest responses from him. This one was deciphered thus: “I am too overwhelmed by your question and cannot answer you so I’m going to avoid you completely by falling asleep.”

It has been almost a year exactly since we last ventured off on a day trip to Montreal (“Midsummer Madness”) and Michael’s condition has worsened – or my energy has weakened – making me wonder if we would ever manage another such journey together. It is only a two hour drive away, easy on a quiet day, but that can seem overwhelming for both of us if he is anxious. And you never know with Michael. He could be absolutely fine or the whole event could quickly devolve into a nightmare. Because I have dealt with more nightmares than I care to count, I usually err on the side of caution and stay home.

But by Sunday my restless, summer madness had reached nearly a peak. I had even been fighting shortness of breath, probably more anxiety than a physical problem. A rare visit to my osteopath last week – who poked painfully and forcefully around my torso all the while emitting intimate noises I hadn’t heard from a man in a very long time – seemed to release tension around my diaphragm. I spent the rest of that day yawning and breathing deeply as though I was taking my very first satisfying breath. I had come up for air and the feeling was so very satisfying. But it was short-lived. By Sunday the old feeling of suffocation had returned.

I propped Michael onto the couch for his usual morning snooze after rousing him from the table. I’ll call Laura, see if she is home and receiving refugees, then reassess Michael’s condition in half an hour, I thought.  In the meantime, I loaded up the car with everything I could think of for a day away with a severely disabled man, then took the dogs outside for a playtime before they might be shut in for the rest of the day.

When he awoke, I posed the question again. This time he didn’t immediately slump into unconsciousness. He merely looked at me blankly.

“Right, we’re going,” I announced. Hey, that was an affirmative response if ever I heard one.

It took only the time to direct him to the bathroom for a final emptying, then I tied his shoes and we were off. From the formation of the idea to actual execution of the plan? Forty-five minutes, forty of which was his nap time.

We arrived home eight hours later. It was a wonderfully successful, simple day, thanks to careful reorganization of the medication schedule and allowing no time for anxiety to mount. “Why don’t I do this more often?” I wondered, vowing without much conviction to make another attempt soon. We sang loudly and lustily together to old songs. I sang alone to the new ones. Michael’s lovely deep voice is long gone and his singing is rather atonal now but I was happy to see he still pitched in occasionally. At one point I looked over to see his air guitar skills being exercised. What is it with guys and the air guitar? Also, since we are analyzing male psyches, what is it with guys – the middle-aged variety, that is – and very expensive top-down sports cars? I would say that ninety percent of such cars that we saw on the road were being driven by older men sporting baseball caps. The young ones, on the other hand, were all driving Batmobiles –  or reasonable facsimiles. I took great pleasure in blasting past a bald head in a Mercedes, I in my newly-acquired bright green Accent, dubbed Joyful Joyce after my recently deceased aunt who would have enjoyed a car named after her, I believe. Not that I’m shallow or anything…

On the caffeine-fueled trip home, an old Joan Armatrading song came up on my ipod, a song I first heard the year I met Michael and associate with him, especially the sexy basso profundo who backs Joan up in this recording, a voice that never fails to reach deep down inside and cause shivers of delight. I told him so as we raced down the road (I had kept my speed under control on the way there but couldn’t resist zipping home). Unable to speak, he simply put his hand on my thigh, an old gesture that used to speak volumes.

“He loved it,” our regular caregiver reported to me upon my return home this morning. The open road had beckoned and I didn’t resist the urge despite the risks. And I didn’t have a single moment of breathlessness all day.

The landscape has changed.

* Swimmer, personification of the Orontes River, Bronze, 2nd century CE

This article is copyright protected and may not be republished without permission.

Visit the authors site or share this article with your friends... Thanks!

    avatar

    Claire - Day To Day With Parkinsons Disease

    One woman's journey as a caregiver to her husband in the advanced stages of Parkinson's disease... Loss of freedom as we have known it is a common adjunct to any disease. In the case of Parkinson's Disease it is the slow degeneration of physical capacity that limits freedom, and later in the disease for some, the cognitive impairment that limits one's ability to make rational decisions about anything, including what clothes to wear. The story of our lives together with this disease is what I hope to bring to you. Be assured that it won't be a tragic tale but I hope one of grace, humour and love for, after all, we are all struggling with life's trials in one form or another. Ours is well mapped out for us at least with all the literature available on the subject. I hope to bring it off the pages of the medical journals and into the realm of the ordinary.

    More Posts - Website

    1 comment to Surfacing

    • i am so sorry you are going through this. i take care of my brother who is mentally challenged, is a heart patient, and also has Parkinson’s. This disease is hell. Even in its best days it is unreliable, and affects all parts of the body mind and soul. my brother wants to die.

    Leave a Reply

     

     

     

    You can use these HTML tags

    <a href="" title=""> <abbr title=""> <acronym title=""> <b> <blockquote cite=""> <cite> <code> <del datetime=""> <em> <i> <q cite=""> <strike> <strong>

    *