Monday, January 09, 2017
Out of hours
It had been a little uncomfortable for him during the night so I suggested he have another hour in bed. We hadn’t anything planned that day other than our usual Friday night take-away in the evening so nothing was spoiling.
When he finally rose at midday, he looked rough. His elbow was now swollen and slightly red yet there was still no bruise to indicate a knock, which was a little perplexing.
John felt a little better in the afternoon so just pottered around in his work room. I was busy working on my laptop and watching some DVD’s in the living room, when he came downstairs at his usual time to head out for the Friday night pizza, or in the case of this particular Friday, Chinese.
Looking extremely grey he asked, “can you check to see if I have a temperature as I don’t feel so good. I’m hot, achy and shivery”.
I hunted out the thermometer from the medicine box but the reading said his temp was normal. I wasn’t convinced so said I’ll try again later after reading the instructions in case I wasn’t pressing the right buttons on it.
“I think you should go to bed”, I said.
“What will you have to eat”, he asked, seeing as there would be no Chinese take-away that night.
I reassured him I would find something and also a way of getting it from the kitchen to the living room – walking with two crutches does limit your carrying ability somewhat....
After getting him settled in bed I went into the kitchen to sort out some dinner. We always keep a couple of frozen pies in the freeze for emergencies so I would have that and some oven chips. While they were cooking I racked my brain as to how I could get them into living room.
I eventually came up with the idea of covering the plate with cling-film to stop them sliding off, then put the plate into one of the large recycle grocery shopping bags. It was a tight squeeze as our new dinner plates are larger than the previous ones. I had intended on slipping the carry bag handles over my fingers whilst gripping Stickies, but the bag kept bashing into them and I was worried the plate would break.
Time to put plan B into action. Using the bag handles I was able to stretch out my arm, put the bag on the floor, walk the couple of inches to the bag then repeat the process until I got to the sofa in the living room. It was an extremely slow process but I got there in the end.
It was about 11.30pm when I retired to bed. John was still feeling pretty lousy so I took his temperature again. This time it did show that he was running a temperature. His elbow was now extremely sore and swollen, bright red and very warm to the touch.
Earlier in the day John had googled elbow pain and everything was hinting at tennis elbow. Given his new symptoms I wasn’t convinced so whilst John was sleeping I got my Kindle Fire out and did some searching.
Whenever I kept putting in John’s symptoms it came up with the same answer – infection, see your GP immediately. It was the early hours on a Saturday morning. Our GP surgery doesn’t work weekends and the earliest appointment to see any GP was four weeks (on Friday morning I checked the status of the prescription I’d ordered online and out of curiosity looked up available GP appointments).
Having suffered at the hands of infection before (eight weeks in hospital and a stay in intensive care) I am a little cautious. Even though it was 1.15am I woke John and explained my concerns.
“What about ringing NHS direct”, I suggested, “they might be able to help”.
I know they’ve had a lot of bad press but the odd times I’ve used them they have been very good.
“It’s worth a try”, replied John.
A couple of press one for this, press two for that later I passed the phone to John. The advisor took the various details and advised John to take some paracetamol to bring down his temperature and arranged for an out-of-hours GP to give him a ring within the next six hours.
The GP rang at 6am and had a long chat with John. Not wanting to blow my own trumpet, I was right. John had an infection of the elbow joint so the GP would fax over to Lloyds the chemist a prescription for some antibiotics.
Having read the blurb what went with the antibiotics I don’t think the GP was taking any chances. There are two strengths of this particular drug. John has the strongest one and has to take two of them four times a day for a week.
I’m pleased to report that John’s feeling a little better. His temperature is back to normal and the shivers and aches had gone. His elbow isn’t as swollen, sore or firefly hot as before. The redness though is still there, in fact its spread nearly to his hand. John, however, was warned that would happen.
Whilst the symptoms of the infection have subsided, he’s been hit by the side-effects of the strong antibiotics, so is feeling a little spaced out. Bless him...
Marie
Monday, November 25, 2013
Monday, September 30, 2013
Long time no hear
As I mentioned in the previous post I was hoping to be discharged from hospital the following day. Everything was going great for me to leave then three hours before we were due to catch our train my wound started to bleed quite heavily. Agnes, my nurse, called Professor Cobb who came immediately. It was now 50/50 whether I would be able to go home that day.
The Prof asked what time our train was. 1.30pm, but as we required assistance getting on the train, we had to be at Kings Cross twenty five minutes before hand.
He had to dash into theatre so instructed Agnes to put a pressure dressing on my hip. He would then come back to see me around the time we would be due to leave to say either yes or no.
True to his word, still in full theatre scrubs, he came back at 12.45pm and checked the wound again. He would discharge me on one condition. I had to let my body heal slowly so had to promise to take it extremely easy at all times. His departing words were he did not want to see me on the ward again.....
We saw the Prof on Thursday as it had been six weeks since my last op. This time around it was a real hard slog as I'd been banned from doing pretty much everything. I was allowed to put some weight on my hip but I had to wear a full leg splint to stop my knee from bending so walking was extremely difficult. Bending and stretching were severely restricted this time too.
Still, he gave me some good news. My hard work has paid off and my hip is fine. Whilst I'm desperate to get out and learn how to walk again I’ve got to take it really easy and use Wizzy more than stickies as he doesn’t want my shoulders and arms overdoing things - he doesn’t know that I do boxing so they’re a lot stronger than they look.... However if I behave myself then I should see a big improvement in my walking by the summer.
There was though one bit of bad news. I'm still not allowed to climb stairs. Whilst there's no chance of the hip popping out the Prof is concerned the muscles aren't strong enough to support my hip so wants me to slowly build them up.
I go back and see him in January so I'm hoping he'll say yes then.
Marie
Wednesday, August 14, 2013
Deja Vu
Thursday, July 25, 2013
Six weeks
Nothing really has happened since I last blogged - hence the reason why things have been so quite.
I've been keeping myself amused with plenty of hand sewing. You can read all about what I've been doing over at my new blog Gertie's makes and bakes
We go back down to see the Professor next week and I'm hoping he will be pleased with my progress, especially since I've been behaving myself and doing what I'm told (so unlike me!!).
I know there's a long road ahead - for a start I still can't put any weight on my leg for at least another three months - but fingers crossed it'll be worth it in the end.
Marie
Monday, June 24, 2013
Back home
Will do a proper update soon.
Marie
Friday, June 21, 2013
Time flies by
I brought with me my laptop, my Kindle Fire, a couple of magazines, two needlepoint cushions (you can see one of them over at my craft blog 'Gertie's makes and bakes'), a Silversea needlepoint glasses case I got free when we were on our cruise last year, a couple of small Christmas card cross stitching and my big cross stitch project, a baby tiger cub.
Ok, it does seem a bit much given that the Prof said I should only be in for about two weeks. However days in hospitals are very long - they are if you're an NHS patient anyway. Last time the day would start at 6am !!!!
Here at the private King Edward no-one comes to wake you up at 6am. You can stay in bed for as long as you like (in fact it's positivity encouraged). The longest I stayed in bed was until 10.45am (Mary my nurse decided I looked tired so made me stay in bed). Once I'd been washed, dressed and had some physio, it was lunch time.
Then there's the afternoon nap from 1.30pm till 3pm. Another round of physio to follow and before I know it, it's dinner time. No sooner is that over then they're asking when you'd like to settle down for the night.
As well as all that the staff are so friendly here that there's always someone popping in for a chat.
Consequently I've hardly had time to touch any of the things I brought with me. Still, I'll have plenty of time to do them, and more besides, given that I'm going to be laid up for several months.
Marie
Thursday, June 20, 2013
Food, glorious, food
The first couple of weeks I was pretty poorly as I was recovering from blood poisoning caused by the hip infections, so food was the last thing on my mind.
Once the infected hip was removed and the IV antibiotics started to work the hospital hoped that my appetite would pick up. Sadly it didn't.
A dietitian put me on high calorie, multi-vitamin and mineral milk shake drinks twice a day to try and get me to eat again. If anything it did the complete opposite as they were disgusting !!!!!
Sweets, crisps, etc were banned on the ward. However they made an exception as they were desperate for me to eat something, anything, so John was able to bring in contraband.
I'm not a fussy eater. I love quite a lot of different kinds of food - Italian, Chinese, Indian, French, a little Mexican as long as it's not too hot. The problem is I hate meat and two veg dinners. Always have done. That was the majority of what the Sunderland Royal hospital served.
The hospital dietitian was so desperate for me to eat something that I ended up having meals taken from special diets - Halal, Kosha, gluten free - as they were anything but bland. I even had meals off the children's menu!!!!
Meals here at the King Edward VII hospital are a little different. Each morning, just after breakfast, you are given three menu sheets to complete (your 'homework' as one of the food servers calls it).
The first sheet is for dinner that evening. You get a choice of three starters, three 'salad' main and three or four hot main dishes. To accompany the hot mains are various choices of side dishes too.
For dessert there's at least four options plus a huge variety of ice cream and sorbets, and to end, six difference choices of cheese and biscuits.
Breakfast can be continental, full English or if you're hungry, a mixture of both !!! For health and safety reasons egg yolks must be cook until it's hard. So no soft boiled eggs or runny yokes are allowed.
Lunch is pretty much the same as dinner. Instead of starters you get the option of jacket potatoes or freshly made omelettes with various toppings. There's several hot or cold main options, with desserts similar to the dinner menu.
If you just want a light lunch then you can order a variety of sandwiches and baguettes.
When John visits he's able to have meals with me as they have 'guest menus' which have similar options to patients.
For dinner tonight I had chicken liver pate for starters; grilled turkey escalopes on a bed of creamy mashed potato, grilled asparagus and a creamy mushroom sauce, with a side dish of mixed salad for my main; and a lemon cheesecake with a biscuit crumb topping for dessert.
I thought you might like to see a photo of how it arrived.You certainly don't get this on the NHS.
Oh and before you ask it was yummy !!!!!!!!!!!!!!
Marie
Tuesday, June 18, 2013
On one condition
The nurses were concerned about my wound oozing a little and that my hip appeared to swollen. He had a quick look then said everything was fine and nothing to worry about.
I asked him about going home as we'd had a chat about it on Sunday. Originally the plan had been for me to stay for two weeks. However by Sunday I was doing so well he couldn't see any reason why I couldn't be discharged Wednesday.
Whilst I would've loved to go home then, sadly John can't get down to London on Wednesday. No problem said the Prof, just stay until the weekend.
I didn't want to build up my hopes as we'd been here many times before when I was last in
hospital, only for something to happen and I couldn't leave. Hence the reason why I asked again.
The Prof's reply was still the same - this weekend. However there's one condition. I must take it easy. Normally with a hip replacement you can't put much weight bearing effort on the hip for six weeks. I'm no allowed for at least three/four months.
Still it's a small price to pay to get my leg back.
Marie
Monday, June 17, 2013
One small step for Neil.....
The physio's decided to try me walking up and down stairs this afternoon and I passed with flying colours. Yeah !!!!
Professor Cobb is really pleased with how thing's are progressing, which is good news. He called in this morning with his two registrars who help with the op. They wanted to see how their handiwork was doing.
Everyone, from the domestics to Matron, is so friendly and helpful. The food is superb and they even have a wine list!!!!!
Marie
Sunday, June 16, 2013
Stepping out - Moving up
In other news, the Professor is very pleased with how things are going, and there is a possibility that we'll be home within a week. Provided Marie agrees not to overdo things ...
John
Saturday, June 15, 2013
Stepping out
All in all, everyone is very pleased with her progress. Her consultant, Professor Cobb pops in at odd times and expresses his satisfaction. Sometimes it seems as though he never sleeps. He performed the operation at 4:30 on Thursday, and called in to see Marie afterwards. Then he was there before 8am the next day. He called in as we were having dinner yesterday (yes - I'm allowed to eat dinner with Marie in her room !!) then called in just before 10am today.
Marie's room is right above the hospital main entrance, and the flagpole is accessed through her window. At 7:25 this morning, a man came in and took down the hospitals own flag and replaced it with the Union Flag in honour of the Queen's birthday parade.
Once she is used to sitting again, Marie says she will start blogging herself.
John
Friday, June 14, 2013
Marie's adventure in the Big City
More updates to follow.
John
Saturday, June 01, 2013
An emotional rollercoaster
No sooner had we put my Mam’s house up for sale, we got a buyer for it less than 24 hours after the ‘for sale’ sign went up. It’s been all hands on deck to clear out my Mam’s things. In the end we had to get a skip to get rid of a lot of stuff as there’s only so much you can give to a charity shop. It was upsetting to see my Mam’s house, the only family home I’ve know, end up as rubbish.
It was quite upsetting saying goodbye to the house as not only was it the only family home I’d known, but it was the last link to my Mam.
In February I mentioned that we’d been to London for an appointment and hinted that it may be good news. I can finally review that it is wonderful news.
The appointment was at the King Edward VII Hospital, (the Queen’s hospital no less.....) with an orthopedic consultant (he’s also consultant to the Queen....) who has yes to giving me a new hip. Given that we’d been told on several occasions that the damage was too severe to operate, Professor Cobb has studied the scans and x-rays, and after performing the actual operation using 3D imaging, is confident he can – in his own words – ‘re-attach my leg’.
The operation and stay in hospital isn’t cheap. You could buy a decent car for what it’s costing us. However if it’s a choice between walking and not walking, then there’s no contest.
My op takes place on June 13th and the Prof is confident that I’ll only be in hospital for about two weeks. As the hospital has wi-fi I’m planning to keep a day-by-day account here on the blog.
Watch this space for more news.....
Marie
Friday, February 01, 2013
There's a frog in my throat
At first I thought it was just a sore throat from the lurgy that we both had. However as the lurgy disappeared, my sore throat didn’t. I developed a horrible cough and started doing frog impersonations...
Our GP practice is very strict on handing out antibiotics so I’ve just got to let Nature take its course.
Marie
Saturday, January 26, 2013
Well note
Thursday, October 11, 2012
The Mod Walker
Saturday, September 29, 2012
A light at the end of the tunnel
Thursday, January 12, 2012
NHS time
I had an appointment yesterday at 6.30pm to see my GP. It was just a review of some new painkillers I’d been taken.
The phone rang at five past six. It was the doctors surgery.
“Hi Marie. You have an appointment with Dr Blake today at 6.30pm”.
“That’s correct”, I replied.
“Unfortunately Dr Blake is running an hour and a half late”.
The surgery closes at 7.30pm.
“I can give you an appointment for Friday morning at 10.10am”.
“I’m sorry but that’s no good”, I said.
“Ok, how about ten to seven this evening….”
Try working that one out !!!!!!!!!
Sunday, August 14, 2011
Medically speaking
Things have been very quiet in the BOGOF household – as usual – so I thought I’d briefly keep you up-to-date with all things medical (a full various of events will appear in the Joint Journal – when I eventually get them written up !!!!)
Not content with being on Kermit’s, the Man Himself and the Back Man’s consulting books, I’ve now on another two - with one more to be added later….
The first one is a pain consultant – other wise known as the Pain Man. My GP referred me to see him as my painkillers weren’t working and she’d ran out of idea’s as to what to give me. He upped the doze of one lot of the painkillers and changed the one’s I take on a night time. I go back to see him sometime in October.
The second consultant is a neurologist – other wise known as the Hand Man (even though she’s a woman. I named her that before I knew she was a female ….). Back in October I began experiencing problems with my left wrist. My GP thought it might be Carpal Tunnel Syndrome so referred me to see the Hand Man.
After performing various tests on my wrist she confirmed it was CTS. I was then sent for a further test to determine how bad it was. The test showed that I had ‘moderately severe’ CTS and the only cure is surgery.
I am now waiting on a mobile physiotherapist to come and fit me with a wrist splint to wear in bed, with an appointment to see a Hand Surgeon to be made once the splint is in place.
I finally got to see the Back Man, having waited a year to see him since my last appointment. When I saw the Pain Man he kindly explained what had happened to my back so I was pre-warned as to what the Back Man was going to tell me. He showed me my MRI scan and no wonder I am in so much pain - the vertebra had moved a huge distance away from my spine….
The only surgery that can be done is to have rods put in my spine and to try and fuse the vertebra together. However it’s a very risky operation (paralysis, loss of wee and poo functions, etc) so I’ve got to think about it and see him at the end of this month. The answer will still be the same as the one I gave him in June – no way !!!!
My ‘count to ten and smile’ attitude to life is getting harder to do. My GP isn’t sure if it’s the cocktail of 31 tablets I take each day that’s causing it or it’s everything just catching up with me. Counselling is out so I’ve got two months to see if things settle down, then I have to go on the happy pills…..
Marie

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