Jim Pedley’s Blog

Out West, writings, gibberish and other wisdom

Archive for the ‘Diary’ Category

New Ideas!

Posted by Jim Pedley on February 21, 2008

As predicted, the engineer -Tony – paid me a visit yesterday and did a magnificent job of trying to make it a little more convenient for a man to be attached to a machine for most of his day…

No more tripping over airlines.  Just a simple re-routing to every room in the house and convenient plug-in points in various strategic areas.

However, I have been told that I must be attached to the machine for at least fifteen hours a day…

This was my mistake, as the visiting respiratory nurse pointed out.  It was nothing to do with the machine’s output setting; it was my stupidity at removing myself from the source of my energy – for safety and convenience…

Anyway, it has already become a lot more livable in our house, and Joan is now pleased as Punch that she does not have to keep a wary eye on the constantly changing positions of the snaking airline.

I feel a lot better, too, because – after all – Joan is supposed to be going through a recuperation period after a major operation, and the less she has to avoid additional hazards like tripping over my airlines and tumbling downstairs, the better.

Until a few months ago, I had an email buddy – George McGinnis - living in Laramie.  He was a friend of my cousin , Rose – the subject of my story “Out West”, which I am currently publishing via this blog. 

George was a little older than me and had been stationed in the south of the UK during WW2.  When hostilities ended and he came home, he went into construction of some kind and became involved in the use of cement.  The dry cement dust played havoc with his lungs and – just like me – George has paid dearly for his post-war Civvy Street way of life.

In other words he was suffering the same kind of complaint that I am – Pulmonary Fibrosis.  I got mine as a result of working in the minature foundries of newspaper printing establishments for most of my life…

Last year, – although he lasted well into his eighties - George died.  I often wonder whether he could have helped me adapt to this new situation.

It really is difficult, trying to adapt to a new way of living, especially when, as the saying goes, ‘ You can’t teach an old dog new tricks…’

Everything has to slow down, such as taking five to seven minutes to climb the thirteen stairs to get to the bedrooms.  And my computer…

But, like it or not, this is my future.  And my wife’s….   And she seems to be adapting with a lot more patience than I am.  I ask myself: why is it that women always seem to be a lot stronger than men when it comes to illness?

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Raising The Output?

Posted by Jim Pedley on February 19, 2008

My doctor paid me a visit yesterday and decided that my symptoms pointed to an inadequate supply of oxygen into my bloodstream.

This is the reason I have been slowly going downhill since I left hospital twelve days ago.  Apparently, it’s necessary for my little life-saver of a machine to up its output to No. 4.  At the moment, it’s on No. 2, which was the supply ordered by the hospital when I was discharged.

While I was  in the hospital I had been strolling around the wards and corridors, minus my oxygen attachment – which had been set at No. 4 for ten days - gleefully looking forward to home and a little walking, and a little working, in the garden.  And I had ordered a mobile supply ready for carrying about should I want to visit the shops, for instance…

Instead, I have been getting steadily weaker, with wobbly knees being the main indication that something was not right.

The other sign of something being amiss was the fact that even with my being attached to the supply, I was still panting for breath at the slightest  exertion…

Well, today I have a team coming – on doctor’s orders – to assess my current needs, and at midday I am hoping to be out of the doldrums and able to start writing about my future physical activities instead of (apart from the next edited chapters of my book) these hypochondriatical – is that a word? – tirades about my bodily condition…

Believe you me, nobody will be more happy to get away from these particular  hypochondriatical ( again, I ask: is that a word?) outpourings than I will…

Meanwhile, here’s another chapter to be going on with…

Catch you later.

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Oxgen A Help?

Posted by Jim Pedley on February 18, 2008

I have just put the phone down after a word with my doctor.  Having spent ten days in hospital after a blip downwards in my Fibrosis problem, and having now a supply of oxygen intalled at my home, I expected a remarkable recovery…

No such luck. 

I seem to have become weaker and weaker to the extent that even to stand up and turn around causes me to pant for breath – and that’s with the oxygen attached!

Obviously, some kind of adjustment is needed, either to the oxygen supply or to me…

I can just hear the wags out there suggesting that I just keel over and give up the ghost. That would seem to be the complete answer to the situation.

Not on your nelly…!

I am supposed to be able, now, to lift a mobile pack onto my back and, with it’s occasional aid, amble around the shops, or take a pleasant stroll in the sunshine.

Besides, I can’t keel over yet;  I have to finish editing the chapters of my book and publish my finished literary effort…

So, to hell with you wags out there.  I’m not ready to give up my ghost just yet.  I’ve too much to do and I want to do all the jobs that I see lining up and receding into the distance before I, myself, fade off into yonder distant blue.

Anyway, my doctor’s paying me a visit about lunchtime so let’s see what he can pull out of the bag…

Meanwhile, I’m just about ready to publish Chapter 18 of “Out West”.  I’d be grateful if you budding literary critics would give me  hand in trying to assess the worth of my effort…

Yeah.  I know.  I should let the book speak for itelf.

I have done, so far…

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Recovery

Posted by Jim Pedley on February 10, 2008

Well, after my ten days in hospital; and a few days enjoying,once again, the comforts of home, I’ve managed to edit another couple of chapters of my one and only book – “Out West”

I know that there are millions of bloggers out there who, probably, have written books for publication on the internet’s blogging facility;  I’d like to apologise to those – especially my American cousins – who may have done a pioneering trek to the West and who, quite probably, have entitled their efforts as I have done -”Out West”.  It’s entirely co-incidental, guys.  Sorry…

But – as I have said in a previous blog – I never intended to create a literary effort.  It was simply on the insistance of my son, Mark, who decided my copious notes (taken merely to help me recall things to tell people back home…) should be knocked up into a book of some description.  Not for publication; just so he – Mark – could read it…

Now, I have to sort out pictures we took and upload them onto my computer for illustration of the chapters I have written.

 I have to find out how the uploading of pictures, to add to something already written, is accomplished.

And I’m no computer geek…!

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Hospitalised

Posted by Jim Pedley on February 8, 2008

I’ve been in hospital.  (Long insincere ahh.h.h accompanied by plaintive Mozart melody on Stradivarius…)  But it’s a fact.

Ten days ago, I was suddenly attacked by a downward blip in my Fibrosis problem and couldn’t turn around without needing heavy breaths…  Joan – my wife – got worried and sent for the paramedics, who whipped me mighty fast into the Emergency Ward at Selly Oak Hospital, Birmingham, UK, where I was later moved to a Respiratory Ward for treatment.

And there I’ve lain for the last ten days, hence the delay in additions to my new blog…

It looks as though my “blip” is going to remain downwards.  A supply of oxygen has been delivered to my home for my personal use…

  Herewith starts a new life and I am trying to construct a new philosophy to cope with my altered physique and surroundings – because, at the moment, there are trails and trails of thin, plastic air tubing tangling itself all over the floor, allowing me to remain attached to my oxygen wherever I may roam within the house…!

But that situation cannot remain for very long.  I have to find a way to control the air hose in the same way I control the garden hose – on some kind of retractable wheel mounted in some inconspicuous but convenient place.

I’ll sort it, somehow.  Meanwhile, anyone out there with, maybe, the same problem, who can give me a few pointers?

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