jmgoyder

wings and things

Another person dies

A few moments ago I found out that a neighbor had died and I got the most terrible shock. His office was next to mine at the university a decade or so ago, but then he retired to run a farmstay. Not so long ago, I gave him my emus because he had bigger yards. He was known fondly as ‘Farmer John’. I have sent a private message to his wife, and will go to the funeral, of course, but am still reeling that he is actually gone.

He left the university to follow his dream of having a farmstay and, with incredible hard work, and his wife’s support and culinary expertise, he made a success of it. I salute him.

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Gutsy 9 – my fantastic bird-in-hand

For those who don’t know, G9 is a peachick who, for some reason (maybe because she was half blue/half white) was abandoned by whoever hatched her. I caught her as she was scuttling, terrified, into the old dairy and pretty much raised her with the hands of Ants and Ming.

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Today, I decided that I would come home earlier than usual from the nursing home. I told Ants I had to go and feed the birds and dogs, and then said I would see him later.

Ants: You won’t come back.
Me: What do you mean? I always come back!
Ants: Not, yes, what car?
Me: Our car, silly!
Ants: How many calves? I need those people for the fireplace
Me: Only ten left to feed. Ming will do it. I know who you mean for the fireplace.
Ants: Are you sure?
Me: Yes, should we ring tomorrow?
Ants: You do it – something is wrong with me.

When I got home, I went straight out to find Gutsy and, as usual, she was waiting for me:

I’d like a word, Julie

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You’re always out and about and I feel ….

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Oh I think I’m going to cry – how embarrassing!

G9!

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Five seconds

Today, I experienced, for the first time, five seconds of what I always knew was inevitable. For five seconds (and I know it was exactly five seconds because I kissed Anthony five times – three on the nose and two on the forehead – all in quick succession, to remind him….)

Ants!
It’s me – Jules!
Ants!

A syllable for each peck of a second.

This is the first time Anthony hasn’t recognized me and, even though it was only five seconds, it is good to have had that little taste of forewarning/arming because I still have time to develop some tactics and hopefully some wisdom.

When I told my mother about the five seconds of unrecognition (yes, ‘unrecognition’ is a word – I checked) she squeezed my hand but I quickly reassured her that I was fine with this first of what will be many unrecognitions. (It’s kind of weird being comforted by your 79-year-old mother about your 78-year-old husband!)

In what I think will be the near future, the challenge for me will be in how to reassure Anthony that I am indeed Jules, his wife, without embarrassing him. I know this because lately he asks a lot for his mother and many others of his family who are now deceased. Sometimes I say they are all well but very busy but sometimes (for example if he is distressed, as he was for his mother again the other night), I will gently remind him that she is gone.

I was thrilled today to have a conversation with a friend of mine, Ann, who now works as a clinical instructor at the nursing home (she and I both left our jobs at the university at around the same time). Ann told me that she has been showing all staff, including domestic staff, a DVD about Parkinson’s disease that explains, among other things, why someone with PD can sometimes walk, and other times be totally unable in which case encouraging words are useless. Interestingly, the DVD also explains why a person with PD may not respond to a greeting, and therefore appear to be unfriendly. Ann told me that she pointed out to the staff that people with PD need time to process the greeting and should, instead of rushing past with a “Hi Anthony!” and disappearing, wait for his response.

After all, it only takes around five seconds for Anthony to say “hi” back.

On the other hand it only took one second for Anthony to say “Rubbish! Throw it out the window” about the cupcakes I made for him last week!

The kiss Yes, I know I’ve posted this photo before but I love it!

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Simulating home

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As you can see we are still experiencing a wintry spring after its false start last week. The weather alerts for Western Australia are a bit alarming with winds of up to 100 kph so I came home a bit early from the nursing home yesterday.

I have begun to arrive at the nursing home by 11am most days now because, with the volunteering, I need plenty of time to wear both ‘hats’. It is working out so well but more about that in another post.

Over the two and a half years since Anthony entered the nursing home, his room has become as close as I can get it to our real home: freshly picked flowers (although I never did this when Anthony lived at home – he did!); daily food treats on plates and a cutting board I keep there; familiar shows on television via the DVD; a well-stocked bar and our own glassware and so on.

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And (my latest idea!) Ming’s 2.5 kg weights. I didn’t expect Anthony to be quite so enthusiastic about this but I was wrong – he did around 20 for each arm with me cheering him on and cracking up laughing at the same time!

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Despite my intention to take Jack, our Irish terrier, in to see Ants, I couldn’t find either his leash or collar that day so I will probably take Blaze instead for the time being.

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Even I am beginning to feel more at home at the nursing home than I am at home, which is really weird! Well, at the moment, it is a lot warmer there.

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Wheelchair walking

Apparently, despite the fact that we are in Winter here down under in the southwest of Western Australia, the weekend will be sunny.

So I have decided to do something new and different and take Ants for a wheelchair walk tomorrow. Not only is this a way of getting him into the sun, it’s a way of me getting some exercise!

Also, I am contemplating using my blog to write more regularly again about how a marriage survives the dementia that comes with advanced Parkinson’s disease. Instead of blathering on about this and that, I will focus my blog-writing into a bit of a PDD theme. 

Since volunteering at the nursing home, I have learned so much and I seem to be in a perpetual state of quiet joy, playing dominoes and cards with various residents, doing the daily walk with dementia residents, rushing in and out of Anthony’s room for quick hugs.

The wheelchair walking will be a test of my physical strength (I am very unfit, physically) and, as the nursing home is close to the beach, and hilly, it will also be a test of preventing Anthony from toppling out of the wheelchair when we are going downhill!

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Smiling

This afternoon Anthony was, as is usual now, in his armchair in his room at the nursing home and a bit confused. I put the heater on, zipped up his jacket, put a rug from home on him and changed the TV station to “Neighbours”. Anthony’s hands were cold, so I took the heat bag my friend Jen made and microwaved it for 4 minutes in the kitchen (staff let me come and go from kitchen area now), took it back and put it on his lap, placed his hands on it and put the rug on top.

Anthony was really drowsy – has been all week – but at one point I was able to rouse him (by punching him gently in the shoulder). His eyes were blank until they met mine and I said, “Ants, I love you more than anyone in the world.” Suddenly my eyes filled up with tears.

There wasn’t much response so I tried again, more shoutingly, “Anthony, I just told you that I love you more than anyone in the world, and my eyes filled with tears, and you ignored me!”

Anthony looked into my wet eyes, and his drooping mouth (caused by Parkinson’s disease) curved upwards into a smile. I realize that doesn’t sound like much but to get a smile from this previously jovial person who is now so disabled, is a small miracle. The only thing that annoys me about this smiling scenario is that I have to work very hard to get a smile out of Anthony whereas Ming just has to walk into his room and shake his hand and – BINGO – Anthony smiles – grr!

I’m so grateful for the decades of smiling we did before smiling became an effort for Anthony – not because of sadness but because of how PD affects the muscles of the face. So nowadays I come into his room with a huge smile every single day.

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A new phase

I think Anthony has entered a new phase of Parkinson’s Disease just in the last week or so. Taking him for drives, or home for the morning or afternoon, or out to lunch, or to visit friends/family has all-of-a-sudden, it seems, become something we don’t do any more.

This new phase is partly due to a deterioration in Anthony’s physical mobility, and his current sleepiness. The transition from Anthony and Julie gallivanting off for the day to Anthony and Julie sitting in his room at the nursing home, watching re-runs of Master Chef, has been strangely enjoyable for me.

Today I had to take Ming to town to get the bus to Perth at 8.45am so I thought I may as well go straight to the nursing home and spend the day there. After seeing Ming off, I found myself in an I-can’t-wait-to-see-Anthony-mood (a mood that is capturing me more and more).

So, for the first time ever, I spent the entire day at the nursing home (from 9am – 4pm). Partly, I did this as an experiment to see if I could cope. But my other reason was to see if Anthony would like me being with him in the nursing home rather than going out; he did! I will now plan all of my writing etc. to be done in the nursing home.

I’m not blogging as consistently as before – hope to catch up soon with blog friends.

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Not buying into Christmas

Such a relief! Today, Ming and I had planned to go into town, get presents for each other and Anthony, get a Christmas tree, a ham, wrapping paper, sticky tape (which I can never find), send a few last-minute cards, decorate the house, find the Christmas tree lights and ornaments (oh where did I put them?) and generally have a frantic, stressful, expensive, horrible day.

But on waking up this morning to a day that was already promising relentless heat, I changed my mind and a bit later I discussed my idea with Ming:

Me: I think we should postpone Christmas.
Ming: What?
Me: Well, you will be in hospital until Christmas Eve … actually maybe we should just skip Christmas this year.
Ming: What? No presents?
Me: No presents.
Ming: No tree?
Me: No tree.
Ming: No turkey?
Me: No turkey.
Ming: No Christmas crackers?
Me: No Christmas crackers.
Ming: Mum, this is such a relief!
Me: So you agree?
Ming: I think it’s a brilliant idea!
Me: Without all the usual fuss we can celebrate Christmas for what it is.
Ming: Do you mean go to church?
Me: Yes.
Ming: Okay, let’s shake on this.

So we shook hands and grinned at each other.

The sense of relief is huge! I don’t have to fight through the throngs at the shops, spend a small fortune on ‘stuff’, don’t have to worry about how the hell I am going to cook a turkey with no oven, don’t have to search the whole of Australia for cranberry sauce, don’t have to spend hours wrapping presents, don’t have to queue up at the post office – ahhhhh!

A bit later:

Ming: But what will we eat for lunch on Christmas day?
Me: Ham sandwiches? I mean Anthony hardly has any appetite anymore anyway, it’ll be too hot for me to eat and you’re a fussy brat.
Ming: I like ham sandwiches.
Me: Good, then that’s decided.
Ming: But Grandma’s still coming on Christmas day isn’t she?
Me: No.
Ming: WHAT?!
Me: I’m joking, you idiot!

Ahhhhhhhhhhhhhhh – now all I have to do today is frolic with the peacocks – yeeha!

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The stove that died

A couple of weeks ago I put the kettle on and it boiled and I made my morning coffee A bit later, I put the kettle on again for my second cup and nothing happened. Anthony’s 1963 stove died quietly.

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Sigh … it is only three years older than I am, poor old thing!

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Here we go again!

Yesterday Ming and I went up to Perth for the pre-op. things – blood and urine, ECG, consent forms for bone graft and bone marrow, consultations with a nurse, a doctor and an anaesthetist and, in the midst of all of these exciting events, I opened the letter we’d been given on arrival.

Well I got a bit of a shock because his surgery is scheduled for next Tuesday, 17th December! This means he will come out of hospital on Christmas Eve, or may be in over Christmas. Ming is elated it is happening before the new year but, with such short notice, I am a bit panicked about organizing things. He has to be in the hospital at 6.30am which means we will have to go up to Perth the night before and stay in a hotel. I will probably book in for two nights so I can see him the next day but then he wants me to come home again (“so you have time to get my Christmas presents, Mum!”)

This revision surgery is nothing compared to the massive scoliosis op. last year so it should be a piece of cake (I hope!) I took his photo this afternoon after asking him how he felt about the op. His expression is difficult to read but to me it says, “Fine!”

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While we’re in Perth, these two guys will look after the farm!

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