jmgoyder

wings and things

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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Monday 9th June 2014

Today I went into town just after lunch to spend the afternoon with Anthony at the nursing home. This has become the ‘norm’ now because a few weeks ago it just became too difficult to take him out and about or to the farm on a regular basis because of mobility problems. Over the last several days Ants has been quite content to just have me in a chair next to him with my arm around him, watching Judge Judy, Dr Phil and, if we are lucky, a good afternoon movie.

I usually stay from around 1.30 – 4.30pm (my new routine) and it beats the hell out of my old routine of taking Anthony on outings, or home, then being unable to manage. Even at the nursing home, I have been told not to lift, move, or even shift him in his chair, because he is now strictly classified as a 2-person lift.

This afternoon I entered Anthony’s room with wine and olives and my usual ‘goodies’ and he was asleep in his armchair. Usually I wake him up, but he looked too peaceful so I just sat next to him and quietly ate all of the olives. Suddenly a nurse entered the room to take his blood pressure because he had been asleep all day. He woke up but only slightly and the nurse and I struggled to get one of his arms free from his jumper because he was so limp and ‘out-of-it’. Well his BP was 190/110 – very high. This, and the fact that I couldn’t really wake him up enough to say goodbye when I left to go home, alarmed me a bit.

On the way back home to the farm, I allowed myself to think that Anthony might be dying. But my thinking of this possibility could not translate into a coherent thought because I cannot imagine him not being here. Despite the difficulties of home nursing, the transition to a nursing home, and all of the mini-traumas in between, I have not yet been able to imagine life without Anthony in it.

My father, Brin, died of a heart attack on this day, 36 years ago. He was only in his 50s.

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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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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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Meg and Ming

Ming (my son) and Meg (my mother) are very good at charades, or whatever they were playing when this photo was taken. I have no recollection of this occasion, but my mother just sent me the photo which I have never seen before! In the good old days, when Anthony still lived here at home, my ma would often come to visit on Sundays. She and Ming would play games nonstop while Anthony and I watched, bemused, amused and sometimes hysterical with laughter. Meg and Ming + Ming and Meg = Inviolable.

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Meg is Ming’s only grandparent so they have a special relationship, as well as very bad taste in eye-glasses. Thanks for the guffaw, Ma!

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Learning how the law works

Today Ming and I met with his lawyer for the second time and his barrister for the first time. The barrister was just as honest and down-to-earth as the lawyer, but she did warn us that jail is a possibility because five children were injured. I suppose there is no point in panicking about this yet as the court date still hasn’t been set (but of course I am panicking). Apparently the police report will be sent to the lawyer and he will send it on to us but I am not sure how it all works. The seriousness of the children’s injuries has been our main concern over the last two months so I guess I hadn’t (until now) realized how serious the repercussions might be for Ming in terms of his charges and sentencing. Thanks for all the thoughts, prayers and comments for our extended family and I’m sorry I haven’t answered all of them. I am also extremely grateful for the testimonials send to us on Ming’s behalf because apparently these will possibly have an impact on the judge’s decision. I am not going to write about any of this for awhile because it’s too difficult but, again, thanks so much for the support!

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This photo was taken two years ago, before everything began to skew.

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Dangerous driving

I haven’t written about the car accident for awhile because I have been too anxious and shaken, and have not wanted to publicize details that might seem like an invasion of privacy. So I haven’t posted photos or named the children for this reason and will not do so now.

For those who don’t know, eight weeks ago today, Ming took his little cousins and a friend for a ride on the back of his ute (truck), then lost control on gravel about 2 kms from home. I do not want to replay the horror of that night or talk about the details. Instead, I want to say how grateful I am that everybody is recovering well despite multiple fractures including spinal and that yesterday we got the good news that two of my nieces got their neck braces off and the one nephew will hopefully soon be able to walk again (but I don’t know how soon). The friend is recovering well from her badly broken arm but her best friend, my niece, will still be in a neck-to-waist brace for many weeks (she is the one who told me to stop inboxing her, beautiful brat!)

My whole family continues to support each other, with humour, empathy, a couple of arguments, reconcilations, renewed love for each other and enormous mutual support. So I am very proud to belong to such a family – my mother, brothers, sister-in-laws, and the kids – where forgiveness and generosity are so natural.

Ming has now been charged with five counts of dangerous driving causing bodily harm and tomorrow we see the lawyer and barrister who are taking his case. My family and friends have provided many character references for him that will hopefully help but we still don’t know the court date.

In Australia there are three levels of driving offences – careless driving, dangerous driving, and reckless driving, so Ming is in the middle. Of course I am terribly worried but I didn’t realize how worried I was until the wash of relief that all of the children will be okay – even my niece who is still in the brace and oh how I wish I could wear that bloody thing for her.

On the cusp of what if? it is difficult NOT to imagine how much worse this could have been. Yesterday, at another family get together, the children all said how haunted they were still and my heart breaks that they have this memory. I guess it will stop any of them from driving dangerously.

Ming, despite being very open about everything else in his life to me, is strangely silent about the accident and seems to just want it to go away. I understand that and I also understand how reading the character witness statements upsets him. Despite his shock and remorse and anxiety about the kids, he has that attitude of moving forward. I don’t understand his resilence any more than he understand my lack of it.

Dangerous driving is dangerous driving so please warn your younger loved ones that a joyride of this type is not worth it.

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Dementia is not contagious!

A lot of people are afraid of dementia, whether it be Alzheimer’s Disease, Parkinson’s Disease Dementia (my husband Anthony’s type), or other variations. It isn’t just the fear of developing the disease one day, it is also the fear of anyone who has the disease.

As someone who worked in nursing homes for many years, dementia doesn’t scare me at all but I guess, if you haven’t had that kind of experience it could be scary visiting a loved one who used to be the life of the party, or extremely energetic, or with a dry, sarcastic wit (Anthony) only to find them either silent or saying what sounds like nonsense.

But it’s not that scary once you get used to it – it’s not! You learn how to listen differently, you learn how to be comfortable with silence, you learn how to love the person again for what he or she is now, instead of pining for an impossible past. You learn to be unafraid, you learn how to give, you learn how to go with the flow, you learn how to treasure each and every moment no matter how bizarre or strange.

“I just want to remember him/her the way s/he was” is a common sentiment expressed by friends and family of people with dementia and this is understandable, yes, but it is also cruel and selfish and horrible because people with dementia are not dead. People with dementia might be confused, cognitively, but there is nothing confusing about the emotional need to be hugged or acknowledged or visited. Why is this so scary for so many of us?

Before this happened to Anthony, and despite my nursing experience, I, too, found it incredibly difficult to visit people I knew who had developed dementia on top of everything else they were already suffering. Can you imagine how terrible it would be to be so sick, so confused, and then abandoned?

There are not too many visitors at the nursing home where Anthony resides and, when I was a nurse, there were very few in the three nursing homes in which I worked. Loneliness is universal and has nothing to do with age or dementia. People with dementia are lonely; people with dementia are human; people with dementia are often aware of the dementia and need comfort and reassurance, or just a hug. A 5-minute visit is enough to make a bad day good.

This is not about Anthony exactly because he gets a lot of regular visits from family and friends but, because I am in there nearly every day, I see the blank, lonely expressions on many of the other residents’ faces and have now made friends with several people there who never seem to have a visitor. I have also made friends with the relatives who do visit but we are a tiny group.

And the point of this little rant? If you have a friend or relative with dementia, please don’t abandon them. They need you. If they don’t recognize you, so what? Just give that person a hug or a pat on the shoulder and then you can go back to your life knowing that you will probably have made that person’s day shine!

BTW dementia is NOT contagious! (Anthony said that to me today).

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When every day becomes yesterday

When Anthony was home yesterday he kept talking to the television. I would come in and out of the kitchen where he was sitting (his favourite spot) and enter an already-there conversation. I was busy with washing and other chores (something I continue to do even if Ants is home, just to keep things normal-ish), but every time I came back into the kitchen he would be talking to one of his deceased brothers, or to the now-dead stove, or to the dogs on the table (hallucinations).

Ming cannot stand it – he just can’t. He says, “Mum, I love Dad but I just can’t tolerate him!” I understand his point of view; after all, he is only 19 and his dad is nearly 78. On the shy side of 50, I am in the middle of this all the time so, when Ants comes home – and I do this as much as possible – I leave Ming with him while I go to the toilet to cry. No, not self-pity – just so hard to remember how good it once was and how bad it is now.

I miss all of our wonderful yesterdays just as much as Anthony does. But Ming doesn’t remember and he has no recollection of Anthony ever being well. Every day, lately, he has asked me for a hug and every day I have given him a hug, even after our ferocious arguments, about the car accident, about many things….

Sometimes it is hard to be positive but I have enormous faith in both Ants and Ming and I think that is reciprocated to me. I hope so.

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Apologizing to a microwave

Now that Ming is living in his renovated shed (which, by the way, is much more spacious than our house!) I am mostly alone. Of course I am out most days, visiting Anthony, or bringing him home, or taking him out, or running errands, or visiting friends but most of the time I’m home alone.

Don’t get me wrong – I actually love being alone and always have. I never feel lonely, have lots of fantastic friends and family that I see regularly and Ming wanders over from his shed frequently (in search of food!) So being alone does not equate at all with being lonely – well not for me anyway.

However, my aloneness was brought into sharp focus this morning when the microwave beeped for the third time (rather impatiently I thought) to tell me that my coffee was ready. I rushed over to it, saying “Sorry, sorry!” Then, as I took my coffee out, I said, “Thanks!”

It was only as I took my first sip that I realized what I’d done, and couldn’t stop laughing.

You will be relieved to know that the microwave didn’t answer me.

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