I shared last week that I had a bit of a surprise that I couldn’t talk about yet. Well now I can! On Monday of this week, I was interviewed about the book ‘My Way’ and it will be airing next week on Radio New Zealand, and also will be available via a link after the show. I will post that when it is available.
This was entirely out of the blue! I had posted an ad on a large group called Chooice, on Facebook, for the book, and within hours had a radio producer contact me for an interview. My first thought was that it was a have, but she turned out to be legitimate and the rest is history!
THEN….I got asked by some people I know (I can’t say who yet sorry) who aren’t here in NZ, for an interview about the same book! I nearly fell on the floor – dreams coming true people!
THEN….later on that day, I was contacted by Alzheimer’s Association here in NZ, and they liked my book so much, they are putting up a chapter on their blog next week. Can we please invent something other than an exclamation mark….!
So, as you can see, I am extremely excited, completely overwhelmed, and very thankful that this little ‘happy accident’ has grown wings and is beginning to fly. Unbelievable – but God.
Just to finish off a mind-blowing week, I FINALLY got to see my Dad, in the flesh, for the first time in three and a half months. He was so sweet, so cute, and kept telling me I needed to leave, then kept talking about the trees we were looking at – funny man!
For those who are interested in delving deeper, go and have a look at becoming a ‘Dementia Friend’ through the Alzheimer’s website. This is something I am deeply passionate about, advocating for those who desperately need it. alzheimers.org.nz/explore/dementia-friendly-nz/become-a-dementia-friend/
In the meantime, for those of you who are in NZ, go and visit The Store to pick up a copy of the book, or grab some fun festive masks for the silly season 🙂
Well, here we are still in some kind of lockdown – in my case, Level three. I think it’s day 63, but don’t quote me!!
We’ve been keeping in touch with Dad via phone and Skype. He is so delightful!! He’s been wearing a cap that isn’t his, but he’s just so darn proud of it 🤣😄 Funny thinking my Dad goes ‘shopping’ in his own ward!
We sing Frank Sinatra songs, I reintroduce him to my husband and children, and he tells me what he’s currently eating. When I tell him he is my father and I am his daughter, that means nothing to him. He smiles. It’s ok, we’re used to that. He thought being a Poppa was a hoot – albeit he has no frame of reference for that either…
Having spoken with his doctor, I was surprised to hear that Dad has been the happiest he’s been in years. He’s joining in with activities, he’s put on weight, and he’s just had his vaccination. A far cry from the man who was rushed to hospital just three months ago. It’s all a bit odd really 🤔
In navigating the highs and lows of yet another lockdown, I for one am so darn thankful that Dad is safe and healthy – and I look forward to my next Skype with him.
I was just sitting in the back of the car while Neil drove, Dad sat in the front, singing his heart out to Frank Sinatra. I was remembering. Times spent with Dad, in the home and the trips that we frequently take him on.
One such time, we went to Waiwera, and found ourselves in an area that was not too familiar with me. It was along a single road, on the beachfront, but in an area that was quite private. We parked the car, and I helped Dad out. It was a lovely sunny day, so we ventured onto the beach, however, Dad seemed a bit unstable, so I held his hand to steady him.
It was odd. I hadn’t held Dad’s hand like that, since I was sixteen years old. One remembers these things. The moments when subtle little changes become the norm, and holding hands with your father was no longer the ‘done’ thing.
But on this particular day, he needed me. And I was there. I guess the little girl in me, needed him in that moment too. It didn’t last long, but it was just us, just a special moment in our collective history, that will always remain with me.
Walking through the home, alongside Neil, I held Dad’s hand again today. He was a little nervous, as we had to walk a different way than usual, but he gripped my hand as I led him through the maze of hallways.
He can’t think of much to say at the moment, but he does remark time and again, how much he enjoys Neil and I! It’s lovely. His shock of hair standing on end, his teeth seemed to have moved and he’s developed a lisp now. His hands, like my Nana’s, are bony and slender. His appetite seems to have returned, which is a big relief!
I knew walking into the theatre, that I was setting myself up for an abundance of emotion and tears. And I wasn’t wrong. But it turns out, they weren’t mine. Well, not till the last five minutes, and then I felt myself crack.
To my left was a young couple, who found the content too much, and left part way through the movie, utterly sobbing. With all of the best intentions, I wanted to go to that young lady and tell her it was ok, that she wasn’t alone. I wanted to give her a hug and tell her I completely understand; but I actually don’t.
You see, for each of us who are the child of a Dementia sufferer, there are coping mechanisms we have formed; there are emotions we won’t show; there are areas where our experiential expertise don’t cover. And therefore, whilst we should have empathy and compassion for all concerned, we shouldn’t go butting our imposter noses into other’s suffering. We need to be invited into the suffering, then offer ourselves to the one hurting.
The movie, ‘The Father’ is a brilliant portrayal of a Dementia sufferer, through his own eyes. I clicked onto that notion with a couple of scenes at the beginning of the movie. As the storyline unfolded, evidence of my own Dad, came raring to the forefront, and I was left feeling somewhat vindicated.
The non stop comparisons. The nit picking. The angry outbursts of swearing and cursing. The silent treatment. The endless demands. The accusations of being up to no good. These are all things that my Dad heaped on me, time and time again. Fortunately I have a wonderful husband, great brothers and a mother with the patience of a Saint – although since long divorced from my Dad – still a loving friend and a great listening ear for me.
If any of you are either curious, or have a loved one battling Dementia or Alzheimer’s, then I thoroughly encourage you to go and see this movie. It helps tremendously. It gives such a compelling insight into the mind of a former intellect, who now is at the mercy of this dreaded affliction. Anthony Hopkins gives a stellar performance, bringing all the pain, emotion and frustration right towards you.
I walked into Dad’s Dementia unit the other day, and there he was, sitting having a cup of tea and biscuits. His hair sticking up like a scarecrow, runny nose and scruffy jumper aside, the smile that greets you, is immense. He’s like a kid in a candy store, and he knows he’s about to have a lot of candy! Always the question, ‘are we going out now for something to eat then a drive up north?’ Always, a kiss and hug and the words, ‘you’re the best thing in the world.’ Of course I am; I’m the Sugar Fairy and Taxi operator! 🙂
Coming back from our afternoon excursion, I was shocked to see a formerly vibrant and active resident, now needing a carer on both sides, to assist her walking. Colleen, was a gummy bear, who refused to wear her teeth; could swear like a trooper; and propositioned my husband on our first day there, asking him to meet her in the laundry afterwards! She loved dancing, and could flirt up a storm; if only in her own mind. It was nothing for her to stroke my arm and do a little jig with me, then start weeping. On the flipside, she could spot me across the room and start marching towards yelling expletives, and promising to ‘get me!’
My heart is saddened, for I know the day will come when my Dad will need that kind of help too.
In the meantime, when he sits in the café with us, his latest fixation is on the ‘fire exit’ sign, alongside the ‘toilets’ sign. His most recent revelation? Toilets are where you go poos and wees!!
One week before we as New Zealanders went into total Lockdown, the Rest Homes and Aged Care facilities made the decision to go into full Lockdown for the sake of their ailing Residents. At the time, we were lead to believe that the Coronavirus, Covid-19 or Sars-Covid-2, was most lethal towards the elderly and infirmed. Unfortunately for our country, this proved to be true. Most of our small cases of deaths, were indeed in the Rest Homes.
Dealing with not seeing Dad was something that I was consciously aware of when our Prime Minister started to make daily addresses to the public regarding Lockdown. Then the day hit when I realised there would be no visiting him at all, and I didn’t get the chance to warn him! However, all was not lost, as I was able to speak to him on the phone, and the home was able to arrange a couple of Skype calls.
Dad was actually quite funny on those Skype calls – he recognised us, but couldn’t understand why our faces were appearing on a computer! The whole conversation lasted three minutes and fifty one seconds.
Yes folks, that enabled me to stop worrying indeed.
When I was able to visit Dad eventually after ten weeks, I had to go through a whole routine of sanitisation, form filling and mask wearing. Dad didn’t even realise it was me until I quickly lifted the mask up so he could see my entire face!
He understood that I wasn’t able to take him out, he actually was more concerned that there were other patients coming up and staring at me, and he was trying to shoo them away J
I have to say, in this instance there was so much unprecedented things happening in our world, but I learnt not to worry about Dad. The staff again, were utterly brilliant and would keep us informed with emails, texts and the occasional photographs of Dad. He was being entertained and kept busy, so that relieved a whole lot of pressure off of me. Phew!