I have had a really horrible week – restless, agitated, depressed, apathetic, confused, overwhelmed etc. Partly this is to do with beginning (again!) to read Eckart Tolle’s book, The Power of Now, and subsequently failing in my attempts to stop thinking which is much more difficult than it sounds. It is also due to Ming’s near accident the other day and my psychosomatic reaction. I miss Anthony so much. I do understand that a racing mind can be detrimental to overall health, especially mental health, but the more I try to stop my mind racing, the more it races – argh! I miss Anthony so much. Also, after many months with being/feeling okay about Anthony being so debilitated, and spending many hours of most days with him in his nursing home room, I have suddenly been struck with a new sensation – loneliness. I miss Anthony so much. I’ve never felt lonely before: I love being alone, and I have so many friends, so the reason for this new lonely sensation only hit me today, and it hit me in a storm of hail-stone memories. I miss Anthony so much. Perhaps, Tolle is right in that every single moment I spend with Anthony in the nursing home becomes the new now and, yes, those moments are wonderful. But I miss Anthony so much.
The party
Last Saturday I invited a wonderful friend, Mike, who has done the painting in this house over many decades, for drinks at the nursing home at 3pm and my lovely friend, Mel, and her daughter, Emily, also joined us.
Of course it wasn’t the sort of party we might have had years ago when Anthony’s mother was alive, where the drinks were over flowing and the nibbles plentiful: champagne, pink gins, cinzano, cocktail sausages, oysters, assorted cheeses, pate, and other savouries. Neither was it the sort of party we had in Anthony’s pre-marriage-to-me bachelor days: lots of beer, roast chicken, steak on the barbecue, and, seasonally, crayfish.
It was a much simpler affair with just the five of us and the unexpected addition of a nephew from Perth, but this small number of people easily fills Anthony’s nursing home room and seems like a crowd. Also, despite the fact that none of us could drink much (or anything at all) due to having to drive home, and my bowl of almonds wasn’t popular, the open bottle of red wine, the wine glasses that I had ready, and a few bottles of warm beer, simulated a real party-of-old. We were all quite lively and attentive to Anthony and, thinking about it now, it wouldn’t have worked with any more people because it would have been too overwhelming for him.
After everyone left and Ants and I were talking about how lovely the occasion had been, I felt I’d hit on a great idea for the future. I could invite a handful of his many friends for the same kind of party every now and then; I might even be able to get a few of his friends and relatives that are a bit nervous of the nursing home to come along. Yes! I need to take the initiative here and do a bit of old-fashioned planning and inviting.
The next day, Mike emailed me this message:
Hey Julie, just a thank you for yesterday at the nursing home with Anthony.
I was happy to see Ants in a great frame of mind he is looking so well as to when I last saw him. I was laughing to myself all the way home with his comments to me when i told him that he waited until he was 55 then got married at 57, and he replied ” you’re an arsehole” he definitely hasn’t lost his sense of humour. I thought he was extremely bright also yesterday.
I’m thinking that the nursing home has done him the world of difference in knowing that he is being looked after so well in his stage of life with old age and all that goes with it.
Sadly yes he would still like to be home with his Julie and Ming on the farm but that is not possible now. We all realize that he is in the best possible care .
Family and friends can still get to visit him there for however long they have time to spend with him so long as it doesn’t tire him out, I noticed yesterday that he does tire out.
I will come see him again soon to stir him up or he to me.
It was good to see you again you are looking bright again since I last saw you on the farm the afternoon you brought Anthony out for afternoon visit.
Today, it was very easy to conjure Anthony’s newfound smile by reminding him of the party. This was our conversation:
Me: Wasn’t it great to see Mike again!
Ants: The food wasn’t good.
Me: Okay, so what do you want next time?
Ants: Hors d’oeuvres, you know, the ones ….
Me: That your mum used to make – yes I get that!
Ants: Is she all right?
Me: Who, Mel?
Ants: No, Mum.
Me: She’s fine, Ants.
Thanks so much, Mike, Mel, Em, and nephew Michael for being part of last Saturdays party!
Jigsawing Parkinsonisms
When most people think of Parkinson’s disease, they think of dyskinesia which is the involuntary movements, tremors and tics that are symptomatic of the disease. Anthony’s version (called ‘Parkinsonism’) is not like this. Instead, his disease is characterized by bradykinesia – the chronic slowing down of movement.
Big words to match small, sometimes unnoticeable, symptoms. To begin with, many years ago now, I deliberately tripped over these words and many, many more – like ‘idiopathic’, ‘hypokinesia’, ‘ataxia’, ‘dysphasia’, ‘mirographia’, ‘akinesia’, ‘palilalia’ – just as Anthony was undeliberately tripping, literally, over his own feet. I didn’t want to know what those words meant back then; I didn’t want to know what was coming. The glossary below is for those who are curious:
http://www.webmd.com/parkinsons-disease/parkinsons-glossary
The first signs were subtle like Anthony’s inability to open the vegemite jar, and his reluctance to drive the car. But then the signs became more dramatic: Anthony’s increasing stoop, strange gait, the drooling, getting stuck in the back yard and being unable to walk back to the house, the hallucinations, me coming home from the local shop to find him face-down in the vegetable patch, Silver chain home assistance, hospitalisations, drug experiments, nightly toiletting shifts with Ming, Anthony’s apologies, his gradual loss of control over his body, his shame and frustration….
All of these things jigsawed into each other crookedly, violently sometimes; we could not get the jigsaw back together again no matter how hard we tried, because already there were too many pieces missing. A simpler jigsaw needed to be built and learning what those many big words meant has helped frame the centre of this new jigsaw, the centre being Anthony himself of course, and his incredible resilience and acceptance.
One of the most wonderful things that has happened lately is that just when I thought Ants had become totally immobile, the staff told me that his nephew, P, visited on the weekend and Ants was able to use his walker to go outside into the sunshine with P. This nephew visits Ants every weekend, but he doesn’t do this out of duty, he does it because he loves Anthony (and I have yet to meet anyone who doesn’t).
Another wonderful thing is that just when I thought Ants had completely lost his ability to speak coherently, I arrived and rushed to give him a kiss yesterday and he smiled his newfound smile and this was our conversation:
Anthony: You are a wonderful person!
Me: Why?
Anthony: Well, you always find yourself in the most extraordinary places!
Me: What – like here?
Anthony: Yes! You always find me, Jules!
The fact that Anthony’s eloquence, mobility and ability to smile all seem to have come back to some extent, after a long period of struggling with all of these things, is quite strange. I write down all of his extraordinary sentences and am thrilled when he can actually walk; as for the smile, it is almost as if my determination to get that brilliant smile back via any means – including slapstick antics, banter, his favourite comedy series, and just laughing my raucous laugh – has somehow tickled his facial muscles into action again. And, like any exercise of any muscle, the more Anthony smiles, the more able he is to smile. Ming has noticed this and so have the staff and everyone is surprised and delighted.
Does this mean Anthony is getting better? Of course not, but it’s a very interesting turn of events made even more interesting by a conversation I had with a resident whose room is two doors away from Anthony’s. She beckoned me over to where she was sitting in her wheelchair and whispered loudly, “I’ve heard a rumour that Anthony is getting most of the attention these days and is the most popular, but don’t let it bother you because we are all treated well.” Then she guffawed enigmatically and I have yet to decode what she meant.
The other day I told Anthony about Gutsy being killed and he kept reaching out his hand to put it on top of mine.
Over and over and over again – his hand, found underneath the blanket that is always on his knees, and my hand bringing his out into the cold air of a heated room, and his hand finding my hand – a jigsaw of interlaced fingers, a smile, a repeated hand tap.
But, when I was telling Ming about this tonight he said he’d seen Anthony earlier today and Anthony was so confused and blah that he almost didn’t recognise Ming!
Ming: I get it with the smile thing, Mum, but Dad was pretty bad this afternoon.
Me: So should we give up then?
Ming: No!
Me: No?
Ming: I don’t know.
Me: I don’t know either.
The above is not an exact rendition of our conversation but, rather, a compression of many conversations over many months/years. Ming, at 21, is always going to be the vital jigsaw piece that has the elasticity to fit right back in and complete the puzzle, or else wing to and fro.
Par
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saw
jig
My dad’s birthday
Today would have been my dad’s 94th birthday if he had lived. He died when my brothers and I were teenagers so he never saw any of our children who nevertheless know him as Granddad. My mother was only 43. Dad was only 57 and died in Intensive Care at the local hospital. He had been admitted having suffered two heart attacks and was recovering when he suffered a third fatal one. The shock and grief of that day is something I will never forget especially as I was on the other side of Australia at the time, in Sydney.
The following portrait was done of a photo taken of Dad a couple of years before he died. We all have the photo and the portrait and my youngest brother even has it tattooed on one of his arms.
Herbert Henry Brinsley Lane, who went by the name of Brinsley but was most often called Brin, was a tall, well-built man who had a presence. He was known for his eloquence and his strong silence, was not particularly gregarious, but very compassionate and generous. His love for my mother is the lens through which I remember my childhood.
He had a Charlie Chaplin way of standing which, as a child, I tried to imitate, and a habit of talking to himself when trying to figure anything out. A strict father, he taught us all manner of manners, especially table manners! But he was a gentle giant.
A radio announcer and high school teacher at Sydney Grammar School, Dad made the extraordinary decision in his early 40s to embark on chiropractic studies and thus began our travels – first to Canada (I was 8) where he completed his chiropractic degree, then to Papua New Guinnea (I was 12) to work as a chiropractor on a mission in the highlands, then to Western Australia (I was 15) where he set up a practice. He was a wonderful chiropractor and if patients couldn’t pay, he would accept milk or apples as payment.
Not long before he died, I was on the phone to him about how much I hated the college I was at in Sydney and, despite being a godly man he told me to come home and to tell the college people to “go to buggery!” Those were his last words to me, unforgettable in the way they still make me laugh, and cry, in that I didn’t make it home in time to see him alive for the last time. At the time of the phone-call, there was no indication that he was ill.
In my writing room, I often look up to my right at the portrait of my father and, underneath, a more recent one done of my mother.
Significantly, Dad approved of Anthony when nobody else did, including Anthony! After all, I was eighteen and Ants was 41. After Dad died, I went back to work for Anthony’s mother, Gar, and the rest, as they say, is history.
I often feel the presence of my dad: when I am having lunch with my mother; at family get-togethers; in the nursing home with Anthony; during moments of hysterical laughter with Ming; during those unexpected moments of intense grief; and when I accidentally speak with my mouth full. Sometimes I imagine that Dad is there/here with me/with us, smiling proudly.
Happy birthday, Dad.
So much for the autumn hiatus!
Well my autumn hiatus didn’t last long did it! Neither did my ambitiousness haha! I had another look at the full-time behaviour consultant job description and realised that although it seemed a perfect fit for me, there is no way I could do it and keep my job at the nursing home. More importantly, there is no way I could do it and spend enough time with Ants. I did email the association asking if it might be possible to job-share the position but I haven’t heard back yet. There was a public speaking/teaching component to the job but there were also a lot of administrative duties (of people and paperwork and policies) and the latter does not appeal to me in the least! I’m much better at being bossed than being a boss.
So that’s that for the time being – maybe down the track I will do something like that but in the meantime it’s back to writing, including blogging, for me. And I discovered a wonderful program yesterday that will convert your blog into a PDF document and it’s called blog2print. In just an hour or so and for less than $100 I was able to convert 2000 pages of blogging, from 2011 to now, into seven PDF documents inclusive of photos. For more money the program will also convert your blog into a hard cover book, or books, but I didn’t want that because I want to be able to edit and revise and rewrite all those blog entries into a book about our personal experience with Parkinson’s disease and dementia. I had already begun the tedious job of copy/pasting bits into a word document but it was taking forever partly because of having to read the blog backwards and getting confused with dates etc. It wasn’t until I googled “how to turn a blog into a book” that I discovered blog2print and other programs that will do what would take hours and hours manually in just a few clicks – extraordinary!
Anyway this discovery also reminded me of how much blogging has become a part of my life. Not only is the camaraderie between bloggers a fantastic source of joy, but if I hadn’t written all of those posts I never would have remembered the chain of events of the past few years. I guess what I’ll do now is to print it out in 50-page sections and do the hand-written editing in the nursing home with Ants, then come home and finish the job on the computer. That way I can add material retrospectively.
Also, in anticipation of a blog break, I suddenly felt quite bereft! It is such a great way of keeping a record of things that can easily be forgotten – especially conversations both with Anthony, the women in the dementia house, and with the Ming.
For example, he rather reluctantly came to find me at work the other day and I let him into the dementia house and introduced him to the ten women who he proceeded to charm easily, simply because he is a male, and young! Oh I am so relieved not to be going for that behaviour consultant job. I work this afternoon and I can’t wait! I have never felt like this about any other job and I am very much ‘at home’ in my OT role now. Even though none of the women remember me, I am greeted with welcome smiles and the oft-repeated “Oh you look so familiar. Have we met before?”
Anthony doesn’t remember who any of the staff are either and the other day introduced me to one of the carers by saying to her: “Have you met my wife?” She and I exchanged a grin and a ‘yes’; after all, we have known each other now for over three years.
Blogging helps me to remember and record these tidbit gems, these moments of pleasure and humour in amongst the pain of illness and age. And autumn is a good time to write and be because it is too rainy to go for a bike ride, Mr Tootlepedal!
It might also be a good time to convince Ming to get himself some new shoes. 
Going, going … gone!
Here are some ‘before and after’ photos of the inside of the two sheds that Dina, her assistant and I cleared the other day:
Shed 1:
Shed 2:
I asked the lovely woman who runs a local heritage park/museum to come out this morning to see if any of the bits and pieces were of interest. She arrived with the man who helps manage the park and they inspected the ‘goods’:
After some mulling and very interesting chats about what some of the once-upon-a-time objects were, the heritage park people picked out a few items of interest for which they were willing to pay, then, with the Ming’s permission (of course!) took most of what you see in the photo away and gave us double the price we would have received from a salvage yard. Brilliant!
At the same time, Dina was here for her last big job with us which was to finish decluttering Ming’s shed/home. Unlike the other day, with the filthy-old-sheds-job, she didn’t have to wear her astronaut costume.
At the conclusion of Dina’s work with Ming today, we chatted over coffee and were all a bit sad that this massive job had more or less come to an end. Now that she’s finished, I feel a bit lost in the ghostly space of things gone, not because I miss the things but because I am going to miss Dina’s regular visits and the euphoria of getting so much done!
One of the most interesting aspects of her service is her summaries and here is an example:
Goyder Services Summary Veranda & Kitchen PDF
I now have several of these summaries that span the two mornings per week, over two months, in which Dina has helped me to move forward. The ‘before and after’ photos in these summaries, and the summaries themselves, are a unique part of her service and a source of joy to me!
Going = rubbish tip (around ten ute/truck-loads now!);
Going = given/sold to interested people/family;
Gone = the feeling of being overwhelmed!
Thank you Dina – ps. Can you help me with the odds and ends left from our work so far?
The gifts
Well I got my bangle! On our 23rd wedding anniversary a couple of days ago, I rushed in to the nursing home with my gift to Anthony of two bananas and asked him if I could have a silver bangle to add to my collection.
As he consumed the bananas, he looked at me quizzically and asked one of his daily questions: “How much money is in the bank?”
I gave him an inflated estimate and he said, “$3,000, but it has to be a two-door, not a four-door.”
“What the hell are you talking about?” I said.
“The Torana,” he said. [Long story – he used to have a Torana A9X which we unfortunately sold before it became a valuable collector’s item and recently our friend, D. had brought him some laminated photos of the vehicle + a couple of Torana magazines.]
“I’m not talking about a car!” I exclaimed, “I’m talking about a silver bangle!”
At the same time my mother arrived with anniversary presents for both of us – a beanie she’d knitted for Ants and a packet of my favourite cheese, Jarslberg, for me.
“Make sure you get a really good one,” Anthony said when he realised I was talking jewellery, not automobiles.
So my mother and I went downtown to the special jeweller’s whose shop I would visit once a year after Ants got so ill, Baroque, and I immediately fell in love with this!
I asked the jeweller for a massive discount on the basis that my husband was in a nursing home and it was our 23rd wedding anniversary, and he naturally obliged. “Done!” I said much to my mother’s shock/horror/delight.
Then we went back to the nursing home, me with my new bangle on, to show Anthony who thoroughly approved of it and my delight and gratitude. After that I went around showing all staff and residents many of whom came into Anthony’s room to congratulate us both and to admire the bangle. It was such a buzz and Ants was thrilled. (The fact that I will have to sell all the old bangles to pay for the new one is beside the point – ha!)
It isn’t very easy anymore to get that whole exciting buzz thing happening with Ants, despite the fact that his ability to smile has come back. But the adrenaline of a bit of frivolous over-spending was just the sparkle we both needed.
One of the most beautiful things about Anthony is the joy he gets out of giving me something. Ming, on the other hand, was thoroughly disapproving of such extravagance!
Wedding anniversary thoughts
In a couple of days it will be our 23rd wedding anniversary. Over the years, Anthony and I have been hopeless at remembering this and my mother usually reminds me! But, even after being reminded, Ants and I have never done the whole anniversary present thing, just as we have never bothered with the Valentine’s Day thing.
Our love story, in retrospect, is very romantic but we have both been a bit cringy about public displays of affection and have never adhered to expectations around both occasions. In fact, until now, we have never held hands in public. Perhaps, having hidden our romance for so long, when I was younger, and having had such a wonderful platonic relationship beforehand, our friendship didn’t require the usual trappings of romance.
I think that when a romantic relationship begins with a platonic friendship, it is easier to manage the ups and downs of a marriage. I can remember years ago Anthony suggesting that he might one day buy me an emerald ring and silly, young me hoping to get this on my 40th birthday. Instead, he bought me a wonderful lithograph that he had always wanted!
After Anthony experienced my dignified disappointment (“You just bought me something YOU wanted!”) he began buying me silver bangles every Christmas and birthday, picking them out himself during the years before he became too affected by Parkinson’s disease to drive into town. So he began to send me into town to pick whatever silver bangle I wanted, which I did, reluctantly to begin with and unhappy with the thought that I was romancing myself! I eventually quickly began buying my annual bangles at just above Anthony’s budget instructions. It was hilarious to watch his expression when I came home and said, “I’ve found one and I love it, but it’s a bit expensive!”
Anthony (having always been extremely tight careful with money), would ponder the situation, look at the picture of the bangle, then at my greedy grin, and say, “Yes, okay, Jules.” These were gleeful moments, mischievous and hilarious and as solid as the silver in the bangles.
In light of our current circumstances – Anthony in the nursing home etc. I was tempted to just pretend the whole silver bangle ritual. After all, that’s what I did last Christmas and for my birthday in January. But then tonight I suddenly thought Ants will get a kick out of giving me a new bangle so tomorrow I am going to find one that is really unusual and take it in to get his approval.
Our romance began when I was 23 and now we have been married for 23 years, so I will get the chosen bangle engraved with 23 – yes!
Dementia dialogues 3
Okay so this post concludes the little mini-series about what I have learned over the last several weeks of working in the dementia house.
Silence is golden!
To begin with, I would take various of the ten women for wheelchair walks around the gardens and through the facility, bombarding them with my chatter and questions, pointing to flowers or pictures on the walls, or just telling anecdotes or jokes that I hoped would elicit conversations.
In hindsight, that was idiotic in many ways. Can you imagine being in a wheelchair, travelling through beautiful gardens, observing the various flowers, breathing in the fresh air, catching a glimpse of the ocean, with the person pushing your wheelchair, whose big shadow you can see on the footpath, chattering AT you, asking you questions that frighten you because you don’t know the answers, disturbing the peace of being outside?
Weeks ago, during one of these walks, I asked D how many children she had and she paused, nervously, then said, “Two or three I think.” She was embarrassed not to know the answer. Then, with S, the same question elicited sobs of “Where is my family?”
So now, unless the person in the wheelchair initiates a conversation, I just shut up and push the wheelchair and, in this way, we are both able to listen to, and appreciate, the silence of the fresh air, the smell of the ocean, the sight of the roses and other flowers.
Silence is golden!
Once back in the dementia house, there is plenty of opportunity to chat, joke, play card games, do jigsaws etc. so I am not quite sure why I felt it so necessary to crowd the quiet fresh air with my clumsy hundreds of unnecessary words. The wheelchair walks will now be done in silence.
The other thing I have learned through working in the dementia house is that touch can be a way of communicating that doesn’t rely on words or even facial expressions. A hug, kiss, hand hold, given to you by a person with dementia, is worth a zillion words – and to respond to that gesture is worth a zillion more. On the other hand, I have also learned that some people flinch at being touched, especially people who are silent, so this is something to be respected; after all, every single person with dementia is an individual. Some people don’t like to be hugged.
I am not going to write about this for awhile because I still feel that I am on P-plates, learning via my mistakes, learning how to appreciate and respect and ‘read’ silence, and learning about individual personalities.
Even though Anthony also has dementia caused by his Parkinson’s disease, I always test my ideas out with him just the way I used to do when I was writing university essays and, later, lectures. With the simple difference between a nod or a shake of his head, he continues to be my mentor despite the fact that his own ability to speak coherently is faltering fast. So learning how to read silence is a necessity.
Silence is golden!
Respect for silence is gold.
jmgoyder 