jmgoyder

wings and things

Silence

Lately I haven’t felt like reading or writing anything much. Despite this temporary aversion to words, I have plodded in and out of other people’s blogs and/or Facebook posts and have begun copy/pasting bits of my own blog into a possible book about Anthony and Parkinson’s disease but the initial buzz of this latest project has abated to a low hum. I know that this is worthwhile so will continue but re-reading the bits and pieces of posts I have written over the last three years of our unwilling venture into the landscape of Parkinson’s disease and dementia seems to have rendered me wordless. I draw enormous encouragement and inspiration from other people’s words but have become sick and tired of my own wilting voice.

The strangest thing about my own silence has been in acknowledging other people’s silence, especially those with dementia with whom I interact at the nursing home in my new part-time job as ‘lifestyle assistant’. Initially (a few weeks ago) I accompanied the wheelchair walks with my loud voice – admiring flowers, pictures on walls, the automatic door, the delicious smells coming from the kitchen etc. But, over the last couple of days, I wheeled various women around the gardens of the nursing home property in silence – just listening to whatever they had to say or, if the person were unable to speak, I shut up too. The unbusy silence of these short journeys seemed somehow wrong at first but I now see how my silence allows whoever is in the wheelchair to smell the roses, see the pictures, hear the greetings of staff, touch the hands or shoulders of other residents, and converse with everyone we come across.

I have never loved a job as much as I love this job, but some of the lessons learned, via the different kinds of emotional suffering people with dementia endure, leave me speechless. Touch has become much more important than words and, even though I am a huggy person, hand massages aren’t really my forte but these really work in calming some people down.

Now that Anthony has entered this dementia phase of Parkinson’s, I am learning once again how to listen better, how to shut up, and how to be comfortable with silence. I really believe in this silence thing now but am not sure. I know that with Ants my silent presence in his room, or wheelchair walking around the grounds, frees him from the responsibility of conversation now that he has kind of lost track of language.

Anyway, perhaps, sometimes, silence IS golden.

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What a strange Christmas!

On Christmas Eve, I sliced the ham and put it into a sealed container in the refrigerator, ready for Ming to bring to my mother’s place in the evening, then I went to the nursing home. Ming was working at the restaurant and planned to come home, shower and change and head to my mother’s while I spent the afternoon with Anthony.

Just after I got to my mother’s at around 6pm, Ming rang and said he was sick and had been vomiting and didn’t think he could come.

“But what about the ham?” I shrilled unsympathetically.
“Mum, I am really sick!” Ming exclaimed weakly.
“Can you just bring it and then you can go to bed at Grandma’s,” I said.
He agreed begrudgingly.

Meanwhile, family members began arriving at my mother’s, champagne was poured and the presents under her Christmas tree were ogled. I kept an anxious eye out for Ming and finally he arrived. As he walked up the driveway, I wondered why he had left his car in the road and why he was wearing such a strange spotty outfit. Then I realised, oh no! that he was covered in vomit.

“I just threw up in my car!” he said weakly, but ferociously. So we got his car into the driveway, he went inside via the back door so he didn’t have to see anyone, and my mother gave him some clothes to change into and put him to bed. I took the container of ham inside then got a bucket of water and tried to clean the inside of Ming’s car but it was everywhere (I will spare you the details!)

Anyway, with Ming in a bedroom adjacent to the loo, the rest of us continued our festivities while I checked on Ming periodically, who was continuing to vomit every hour or so. I felt terrible to have made him come and had to suffer his weak remonstrances of “You care more about the ham than me.”

By the time I was ready to go home, at around 9.30pm, it had been decided that Ming would sleep the night at Grandma’s.

The next morning (Christmas day) at 6am, there was a knock on the front door that woke me up and, assuming it was a recovered Ming who had lost his key, I opened it blearily only to find it was my brother! He said, “I thought you might like some company – let’s have a drink.” So BJ and I drank champagne on the front veranda, waxing lyrical about this and that and watching the birds dive in and out of the trees, including the new wild parrots I’ve never seen before. It was a fantastic hour and it actually made my day! Then BJ had to head home for his family’s 8am Christmas present ritual.

After he left, my mother contacted me to say she would bring Ming home because he was too weak to drive and had continued vomiting until 4am. So they arrived and we opened a few presents but Ming was still feeling ghastly so I put him to bed and my mother headed in to town to my brother’s place after which she was to meet me at the nursing home.

Well, the crayfish, mango, and my mother’s pavlova, were all a great success with Anthony and so were all the presents I helped him unwrap, then we watched a bit of tenor music on TV, then my mother left, then I went to do my 3-6pm shift in the dementia wing.

After I knocked off, I went back to Ants’ room and we ate the leftover crayfish (which I’d put in the staff frig.) and I went home to my no-longer-sick-but-very-weak son who struggled through the opening of his remaining Christmas presents ha!

But yesterday my mother contacted me to say she had the same thing – the gastro. and it was absolutely horrific and I was helpless to help because of contagion. I rang the nursing home to tell them the situation but that I, myself, was not affected (there is a strict rule that you don’t come in if there is any likelihood of infection of any sort). So, despite the fact that I’m not sick, I’ve been banned from coming into the nursing home until next Thursday! This means I can’t do my allotted shifts and can’t see Ants.

Thankfully, my mother is over the worst but is obviously very weak. Today Ming and I are going to hers to pick up his vomit-ridden car but, now that he has recovered, he wants to take me out for lunch first.

What a strange Christmas!

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Applying for a job

As many of you know, I recently applied for a job at the nursing home where Anthony has now lived for nearly three years. The job is that of ‘lifestyle assistant’ in the dementia wing/house, a role I have been learning over the recent weeks of volunteering. It is a three-hour shift, between 3 and 6pm, often a time of restless agitation for people with dementia as the sun goes down (Sundowner’s syndrome).

It was such a strange experience to be interviewed on Tuesday by two women who I already know so well – the Manager and the Events coordinator – but I still said “lovely to meet you”, which made us all laugh my nervousness away – well, sort of! But then I answered some of the questions clumsily, ignorant of the fastidious rules that have come into play since I last worked in a nursing capacity over 20 years ago.

So I was pretty sure I muffed my interview up and almost felt a sense of relief, but I couldn’t help hoping. Anthony knew about my application and interview but was a bit unsure about what was going on (he is not in the dementia wing) so when the Events Coordinator came into his room today and asked if she and I could have a chat, I thought she was just going to tell me I didn’t get the job.

And that’s how she started:
Ev: Julie, about that interview the other day (pulling a looooong face)
Me: Yes? (trying to look nonchalant)

But this is how she ended:
Ev: You got the job.
Me: What?

After that I twirled around Anthony’s room in a state of glee and, because I know so many of the staff and residents anyway, it’s been a joy to whisper, ‘I got the job!’ and Ants said at one point, “You are wonderful, Jules”.

Note: This is first post since my computer died and my computer whiz guy has salvaged everything onto a usb thingy. In meantime I have bought myself a Macbook – brilliant!

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Saying ‘yes’ to surreality

Ever since I was fooled by the plum tree into thinking its blossoms belonged to the avocado tree I am much more aware of how trees that are next to each other seem to have a habit of hugging each other. Here are the photos I took of ‘the avocado blossoms’ several weeks ago. The first one shows why I was confused but the second one shows quite clearly (except to an idiot – me!) that these are two separate trees.

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Anyway, the following photo shows just how tricky these trees can be; here we have a camellia tree masquerading as a fig tree (or is it the other way around?) I showed it to one of the residents in the dementia wing the other day and she said, “What a strange tree!”

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Up close, of course, it is quite obvious that the fig tree is a fig tree and that the camellia tree doesn’t have a sense of personal space.

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Last summer I stopped watering the plants in order to save electricity on the pump; hence most of the ancient rose trees have died (despite a gardeningy person telling me it was impossible to kill roses) but everything else (palms, multiple camellias, un-fruiting orange and plum trees, silver birches, the two fig trees, the two avocado trees, the two pear trees, the lemon tree, the poplars up the driveway, the flame trees, and many other wild bushy looking shrubby things, have survived. This is probably because Anthony planted many of these at around the time I was born – over 50 years ago – so their roots are deep (you see, I have now done a bit of gardening-for-dummies research).

I guess what’s surreal is that, when I took ‘the avocado blossoms’ into the nursing home and put them in a vase, Anthony didn’t correct me and say, “Those aren’t avocado blossoms, silly!” (Actually nobody corrected me until I wrote a post correcting myself and then a friend said to me, “Yeah, I thought you’d definitely lost the plot!”)

Every single person with every single kind of dementia has, I think, has an ability to accept the surreal as real. Yesterday, during a children’s concert at the nursing home, one of the residents kept asking if the woman on my right (another resident) and the man on my left in the wheelchair (Anthony) were my parents, so I explained that one was my new friend and the other was my husband. She looked at me with interest and said, with absolute certainty, “My parents will be here soon”, and I said, “Yes.” By end of the concert she had forgotten about her parents and was fine, delighted as we all were, by the children’s voices.

I’m not sure here, but it seems to me that if someone’s reality is fractured by dementia, and their reality becomes a dreamscape of surreal thoughts, memories and emotions, maybe the best way to respond is in the affirmative, and to say ‘Yes!’

And that is why I still have an avocado tree with pink blossoms!

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Before and after!

Ming has spent several months travelling to and from Perth to audition for a variety of acting roles, and to undertake training in this field. For much of this time, he didn’t have a car or car licence so took the train or bus and either stayed with kind relatives and friends or at youth hostels. Now that he has his licence back and his cute little car, going to Perth and back has been easier and he has been relishing his independence.

But now that he has this full-time job at the restaurant (which he loves!) he has decided to put the whole acting thing on the back-burner so he has now had his acting hair cut off

Before (this photo was taken at Meg’s 80th a couple of weeks ago):
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After (this photo was taken tonight):
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The new smile

For the love of smiling!

I took a photo of the avocado tree a few weeks ago and posted it on this blog, bragging about its amazing blossoms. A few days later, on climbing the tree to pick one last unreachable avocado, I got a bit tangled in the blossoms and, in untangling myself, realized they were actually the blossoms from an adjacent plum tree. I haven’t wanted to admit this until now because I am so embarrassed. I am quite sure all gardeningy people spotted my error but were kind enough not to say so. Anyway, it’s not my fault that the plum tree (or whatever it is) keeps throwing its pink-blossomed arms around the avocado tree!

I was overjoyed to spot a little peachick on the roof of the shed adjacent to the chookyard and I had a rather long conversation with it until I realized it was a twig!

I love to tell these embarrassing little funny stories to Anthony because it gets him smiling. Some time ago, it seemed that he would never smile again – not because he was sad but because the Parkinson’s has affected all of his muscles, including facial. But over time, I have learned how to elicit a different kind of smile; I use banter, loudness, crudeness and lots of vigorous hugs.

His loud, spontaneous, contagious laugh has gone and so has his loud voice as he now speaks in a kind of whispery way but I am ungentle and say things like:

Speak up, Anthony, clear your throat!
You look like a dead duck today!
Wake up!

Sometimes I catapult myself into his room, throw my arms around him and he gets such a shock and always says, “Jules, how did you know where to find me?”

Or, if he is having a bad day with forming words, I just get his beautiful new, slow-growing smile. And when Ming enters the room, Anthony’s smile gets a whole lot quicker!

Note: Avocado trees do not have pink blossoms!

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Catching up

After weeks of fighting a tenacious flu that kept coming back after each course of antibiotics, I finally got a chest x-ray which was clear (phew!) but my dr seems to think it was probably a case of pneumonia treated with the wrong antibiotics (I saw another dr to begin with because mine wasn’t on duty). So now I am on a fifth course of two different antibiotics and already feeling a lot better instead of a little bit better. It is such a relief because, despite being well enough for my mama’s 80th b’day and well enough to visit Ants most days and to do some volunteer work, it is only now that I am beginning to feel normal well ha!

As my role as ‘care-giver’ has become most of my identity now, I have a bit of a terror problem when I get sick because I am so needed by Anthony so to have been given the gift of a clear chest x-ray is like gold!

I’ve been trying to catch up and re-connect with blogger friends but have now decided to simply read blogs in a from-now-on mode rather than go back to see what I might’ve missed. It’s been a bit of a relief, too, to let go of the self-imposed feeling of obligation to blog every day if I just don’t have the time or inclination. Perhaps someone should write a book about blog psychology because I get the impression that other bloggers often suffer the same kind of ridiculous guilt. Interesting.

My volunteering at the nursing home, though interrupted by this flu, because you are not supposed to go in there if you are sick (paradoxically, this is probably where I first got infected), continues to delight me and I have now sent an ‘expression of interest’ email in response to last week’s advertisement for a “lifestyle assistant” in the dementia wing. This is a permanent part-time position from 3-6pm for someone to provide activities while the nursing staff conduct the evening showers. As I have already been volunteering in this wing from 3-4pm on the weekends, I am familiar with each of the ten residents and have developed a bit of a rapport. Tomorrow I will fill out the application form and hope for the best. I think this kind of arrangement would be a perfect match and hopefully there will be no perceived conflict of interest as Anthony is not in the dementia wing. I am quite excited about this job possibility and the money would be a relief!

Ming has a job he loves at a restaurant called ‘Corners on King’ so he is gradually becoming independent financially and in other ways. He hates for me to make him any food so my tactic has been to make him a smoothie every morning into which I pack a punch of secret ingredients (if you want to know the secret ingredients you will have to email me!) For those who don’t know, Ming has, from birth, had a rather extraordinary unhungryness – long story which I can’t be bothered telling now but my best illustration of this is the 40C degree day, when he was about one, in which Ants and I had to use a syringe to push a bit of milk into his ungreedy little mouth.

The last few years have been enormously challenging with me having to resign from my job as university lecturer; Anthony’s permanent admission to the nursing home; my mother’s horrifying injuries after falling from her bicycle; the car accident and court case and cousins’ heroic recoveries; Ming’s two scoliosis operations; some friendships rekindled and others on hold; peace, joy, guilt and wretchedness in equal amounts; Ming’s short-lived, but loved, dairy worker job abandoned due to his spine; finding out that you really love eggs on toast; and that if you don’t like what you look like, you need to stop looking at yourself and look away…..

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…. and finding out that the width of hope is immeasurable!

Catchya later….

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Memory Lane!

One of the most extraordinary things about my mother’s 80th birthday last week was her gifts to us! To each grandchild she gave beautiful engraved keyrings, and to each of her children – my two brothers and me – she gave a photobook and a CD of photos of our childhood in Canada and Papua New Guinnea. None of us had seen these photos from 30-40 years ago because most of them were on slides; it must have been a hell of a job to get them Cd’ed and it was such a wonderfully unexpected surprise! I keep looking at all of the photos with a mixture of nostalgia and joy; actually I can’t seem to STOP looking at them because I am gobsmacked at how cute I was haha!

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One of the best things is to see Dad again; he isn’t in many of the photos because he must have taken most of them – our wonderful father, Brinsley Lane, who died suddenly when we were still in our teens and Mother was just entering her 40s.

Her gift to us is, of course, ongoing – a rich and vibrant record of a strange, varied and unpredictable childhood that is/was so much like Narnia – magical!

Thanks Mama!

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What a peculiar blog!

I have just looked back to discover that tomorrow will mark the third anniversary of this blog. The reason I was looking back was because I want to find, in amongst all of the bird stuff, everything I have written about Anthony and Parkinson’s disease and how he, Ming and I have coped. I thought it might be useful to compile these entries into one document and see if it works as a whole, maybe as a book. Apart from the wonder of all the friendships wrought via blogging, it has also been wonderful to find that I have a record of these past three years because I don’t think I would have remembered otherwise, except as a kind of blurry fog of joys and sorrows – mostly joys.

The birds, and the wings idea, have punctuated the last three years in real and metaphorical ways. Many have now been lost to fox attacks, I have given the emus away, and all three of the original caged birds have been set free. We now have a dozen peafowl, nine guinneafowl, five geese and one duck. The casualties have been heartbreaking and I have decided not to acquire any more due to their vulnerability to fox attacks. Gutsy9 is still thriving and one of the two peachicks hatched last year has survived and I think there will be more chicks soon. I have stopped interfering in the way natural selection works. All of the birds still take bread out of my hand and give me enormous joy (except Godfrey, the gander who likes to bite me!)

But everything changes and now that most of my daytime hours are spent in the nursing home, the birds and I don’t commune as much. Hence, when they hear my voice, they come running AT me with a mixture of love and greed (for wheat) that it is hilarious to watch. And even the birds who are gone continue to live on via Anthony’s hallucinations. Almost every day he points them out through his nursing home window. The outdoor tables and chairs become turkeys; the lawn is speckled with chooks and guinneafowl; and the flowerbeds are parrots. I can see them too.

It seems a rather peculiar blog in its higgledy-piggledyness and some of my entries make me cringe, but hopefully I will be able to draw out enough of the love story to compile a coherent record that might be helpful to others who live with Parkinson’s disease.

Here is a picture of the nearly grown up peachick, still very much attached to his mother (in foreground)!
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Out of the mouths of babes….

This group of quotes for Gma’s birthday book does not need any explanation from me.

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There are more quotes to come of course – from some of the bigger ‘kids’ – but I will save those for tomorrow night after the boat cruise. Suffice it to say that these children’s words, enclosed in her book (and rather brilliantly photographed by me – ha!) have culminated in the most beautiful, mutual, unshakable hug of family.

Oh, I can’t resist: here is Jared’s (Meg’s second grandchild):

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