Author Topic: ArtyMar's blog: buying the dream  (Read 122085 times)

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Offline SteveJ

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Re: ArtyMar's blog: buying the dream
« Reply #250 on: October 24, 2015, 07:07:54 AM »
you owe me a box as well  :)



Offline gillian handbury

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Re: ArtyMar's blog: buying the dream
« Reply #251 on: October 24, 2015, 14:29:54 PM »
Oh No!!! ArtyMar...I hope it's buy one get one free!!! Ha! Ha! .x if not SteveJ you can share mine....

Offline ArtyMar

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Re: ArtyMar's blog: buying the dream
« Reply #252 on: October 24, 2015, 17:13:09 PM »
  :) I'll bring along a truckload, don't worry!

Offline ArtyMar

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Re: ArtyMar's blog: buying the dream
« Reply #253 on: October 29, 2015, 12:54:40 PM »
October 2010  London

BLOG 40:  Good signs

Now there’s no doubt about it. He’s responding, and more clearly. Even King-of-the-Jungle agrees. OH is not opening his eyes, but the squeezes are much more obvious. Hurray! I send out a group email to wider family and friends and get a deluge of responses. The waiting game goes on, but we’re excited and optimistic. I know that OH can hear us and that he is willing himself to return to us. That’s all I need. I feel sure that his other senses and functions will return – however long that takes.

He’s now been in the ITU for 6 days. When the team considers he has recovered sufficiently, he’ll be moved to an intermediate critical care ward before being moved into the general ward. We just have to remain positive and be patient, not so easy to achieve. Strange to think that the merest squeeze of an eye can bring such euphoria, but it means so much. Not only that he can hear, but his brain is functioning well enough to be able to follow an instruction, despite the onslaught of surgery to his body.

My dear optimistic friend, King-of-the-Jungle, again cautions against being over optimistic – he says OH is far from being out of the woods. They don’t yet know just how well his brain is functioning, never mind his kidneys. Also the longer he is unable to walk, the weaker his leg muscles will become. King-of-the-Jungle is a prophet of doom alright. Maybe working in an environment where a number of patients die causes him to be the way he is. Maybe in the past he gave patients’ families false hope and when the worst happened, they turned on him. Who knows? At any rate, I feel certain that OH has turned a corner and will continue to make progress. He is now largely breathing on his own, another good sign. We absolutely refuse to be downhearted. I even find myself thinking momentarily of our villa being built slowly but surely in far away Fethiye. I wonder how it’s getting along having received no photos for a while. Maybe the lack of photos is because I’m no longer emailing L constantly – pushing, pushing, pushing for news. Maybe it’s because the weather is bad there and little building is going on, perhaps the true reason. Anyway, I dismiss these thoughts almost as soon as they surface. When OH is better, I’ll have time to attend to other matters. For the moment, it’s his progress that is important, not that of the villa.

If OH continues this progress, we tell ourselves, he’ll soon make it to the next stage, and be out of the ITU!

Sadly, we hear that Mavis’s Dad has passed away. It seems she, herself has severe OCD and lives at the hospital in the mental health ward. The young guy on the other side of the curtain is still in a coma.

OH, though, is improving!

. . .  to be continued  . . .usually posted on Thursday


Offline echogirl1

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Re: ArtyMar's blog: buying the dream
« Reply #254 on: October 29, 2015, 18:17:46 PM »
Another great post, good news at last x

Offline gillian handbury

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Re: ArtyMar's blog: buying the dream
« Reply #255 on: October 30, 2015, 19:54:11 PM »
Stay strong! Stay positive!! R & G....x x

Offline ArtyMar

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Re: ArtyMar's blog: buying the dream
« Reply #256 on: November 05, 2015, 13:01:36 PM »
October 2010  London

BLOG 41:
  The Miracle Man

After the excitement of finally seeing some progress for the better, reality (King-of-the-Jungle-style) sets in.

It will be a long, slow haul. OH is now out of the ITU and is finally in the general surgical ward in this specialist hospital. The NHS is never perfect but nevertheless is a wonderful institution, no doubt about it. He is receiving excellent care – but he is unbelievably weak. He’s off the oxygen, no longer needs a breathing tube or dialysis, and his kidneys, though weakened have not been permanently damaged. As to brain damage, if any, too early to tell as he is too weak to speak more than a word or two. He still has a number of tubes coming out of various part of his body and due to the numerous operational procedures (opening and reopening and closing the abdomen) he has been left with a large incisional hernia i.e. there is no longer a functioning muscular wall to the abdomen to hold the organs in that region in place, so when he is eventually able to stand up, he’ll look like a pregnant man in the final months! His previous surgery (before this massive operation) had left him with a relatively small incisional hernia due to the decision to use a mesh rather than stitches – which was a new procedure at the time. Unfortunately, the mesh broke before leaving hospital and another operation to fix that small hernia was unwarranted. Before this op, we had hoped that , as an incidental part of the surgery, the hernia bulge caused earlier could be eliminated. Now, that hope has been dashed and he has been left with a much bigger hernia! He is unaware of this, of course, but it is a tiny price to pay for being alive.

Daughter is still with me. She has put her family and work life on hold in the US and comes with me every day to the hospital. Sons and other family come in the evenings and weekends whenever they can. Our lives have narrowed down to the routine of hospital/home/hospital/home.

I’m in the ward. Daughter has gone to get us some coffee. The prof sweeps in with junior doctors and medical students in tow, like royalty accompanied by his courtiers. He pulls the curtain around the bed and I offer to go but he waves this aside. He addresses his courtiers: “and now I’d like to introduce you to the Miracle Man!” He then goes on to tell them of all the difficulties, trials and tribulations he had in OH’s operation and I can tell from the admiring looks on their faces, that they think that he, not OH is really the miracle man. There’s no mention of the Aussie doctor or other members of the team at all.

The nurses are trying to get OH to sit up but this is both too painful and exhausting, even though he is supplied with a special battery device with an inflatable cushion under his bottom to make it easier. The latest medical research, it seems, shows that no matter how major the operation, patients must get out of bed soon after the op, even if that is just sitting on a chair next to the bed. Easier said than done. OH is so weak that even when he is heaved out of bed, with all his tubes and drains and special seat, he just flops sideways over onto the adjacent bed. As to standing, never mind walking or talking, that seems a distant goal. The physios, a cheery team of two, a man and a woman, visit the ward every morning and afternoon. They valiantly try to get OH to sit and give him encouraging words, but to no avail. He flops back down again, sideways onto the bed. When they go, we carry on, urging him to try to sit up for a few minutes. He murmurs “tired – bed” and flops right back down.

“Come on, Dad. You can do it. Just sit up straight while I count to three” says Daughter and begins to count “One . . . two. . .” Flop. We straighten him up, he’s like a rag doll, a pregnant rag doll (with his new incisional hernia).  “One . . . two. . .” Flop.  “Tired – bed”.  So, after about 10 more minutes looking at him flopped sideways onto the bed, we call for the nurses to help him back. He is fast asleep within a minute.

Food is an even bigger problem. He’s too exhausted to eat, so he’s mainly being given special fortified milk based drinks to drink through a straw. Ha! Not so straight forward either. 1) he needs to sit up a bit to drink 2) he’ll only bother when the drink is lifted to his lips and strongly urged to drink and 3) he only tolerates two of the six varieties available: banana and strawberry. Doesn’t like vanilla, chocolate or worst of all, the apple flavor.  Luckily, this ward lets relatives in throughout the day, though there is a sign on the door saying that there is no visiting allowed during the two hours when lunch is taken round to patients. That is just the time when relatives are most needed! If we weren’t there, OH would neither eat nor drink. Evidently, others feel the same, as during the lunch period, many patients have relatives at their bedside – with a number consuming home-brought meals. There’s a strong smell of curry and I don’t believe that the catering team serve curry at every meal! Anyway, this rule is obviously relaxed due to the benefits that relatives obviously bring to the hard-working nurses and auxiliaries, particularly at meal times. It doesn’t bear thinking of as to the fate of some other patients who don’t have the benefit of relatives at their bedsides during meal times.

OH is losing weight. The nutritionist comes to the bedside during one lunch period. She looks sternly at OH, lying comatose in bed after the effort of trying to sit up. We, Daughter and I, have been trying to get him to drink his ‘lunch’. “Not good enough!” says the nutritionist, turning to OH. “You need CALORIES. CALORIES! CALORIES – to heal the surgery”. She adds an item to his daily diet sheet: the list of drinks and soft food that he doesn’t much touch. The item is a small carton of double cream to be had with every meal. OH finds eating solids too tiring but he used to like the occasional jelly. Maybe if I bring that, we can add the double cream to it as an easy-to-eat dessert.  The other thing he likes is my sister-in-law’s homemade chicken soup so when she comes she’s always armed with plenty which we label with his name and keep in the hospital ward fridge. I doubt it has too many calories though, even if it is nutritious.

If he doesn’t begin to gain weight soon, we’ve been warned that they’ll have to feed him by tube, another onslaught which we feel will be a retrograde step.

Come on, OH! Eat! Drink!  Sit up! You can do it!

Oh, yes, and while we’re about it – you have to stand up and walk, too!

. . .  to be continued  . . .usually posted on Thursday

Offline babcc

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Re: ArtyMar's blog: buying the dream
« Reply #257 on: November 05, 2015, 15:34:20 PM »
So even thogh I am leaving work a little early today for a Year 10 parent'e evening (yikes) and am meant to work through thought I would just check into the forum and then remembered I had not checked your blog for a few weeks so just had a maor catch up.

Your writing so captures all the drama, love, stress and all other  emotions that you have all gone through.  Is it bad to say I cannot wait for the next instalment?   Barbara xxx


Offline ArtyMar

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Re: ArtyMar's blog: buying the dream
« Reply #258 on: November 05, 2015, 17:11:54 PM »
babcc! It is absolutely not bad to say you can't wait for the next instalment! I love receiving feedback - makes the writing and reliving so much more fun. I regularly check my hits (now up to 16,125) and get a kick out of the fact that people are actually reading all my stuff - never mind whether they like it or not. It's great to have fans!  ;)

Offline Bluwise

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Re: ArtyMar's blog: buying the dream
« Reply #259 on: November 05, 2015, 18:52:40 PM »
I am a definite fan of your writing Arty - love it!!




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