Leaving our Loved Ones “Sad and Sick…and Lost”
Every time I visit 82-year old Ruth Cuddlepot I read this poem.
She has it up on a wall in her kitchen near the toaster, just above the bench. I know it by heart now because it’s so hard to miss and I stand there every Wednesday reading it (at least three times over) – while I’m waiting for her crumpets to pop!
It’s a short, but popular verse and most experienced carers have encountered it on their travels in and around the Aged-Care industry. To be honest, I always end up feel annoyed after I’ve read it because as far as describing the hopelessness and grim reality of Alzheimer’s disease – it’s pretty spot on.
It is also completely SAD.

So, the story goes that back in her day, Ruth Cuddlepot forged for herself (and prospered for many years in) an outstanding career as a Headmistress in some posh private school for boys – at the time the only woman on record to obtain such a role. She never married, didn’t have children and had no real family to speak of. Therefore, a very well-to-do Ruth had mountains of cash and high-performing investments squared nicely away for that one ‘rainy day’ when she just might need it.
That drab, dreary, drizzly day came a few years back when Ruth received the official crushing diagnosis of Alzheimer’s Disease. Being the no-nonsense insightful person that she was however, Ruth decided immediately that she would face her destiny head-on and set herself up for the inevitable; for when she could no longer work or take care of herself.
Indeed, there would be NO nursing home for Principal Ruth Cuddlepot!
Without wallowing in self-pity and in typical Headmistress fashion, Ruth seized control to ensure her affairs were arranged down to the very teensiest detail. The health services, neurologists, an endless supply of support workers and the most fastidious fleet of solicitors were all put in place so Ruth could be completely looked after and cared for IN HER OWN HOME.
No matter what.
She knew her condition would deteriorate; that her memory would crumble, and she would eventually “lose my marbles completely!” Apparently, that’s how Ruth used to brazenly declare it, although I didn’t know her then and have relied on verbal reports from other carers to fill me in on all the background reading.
Needless to say, she was one very smart woman. Although, by the time I had the pleasure of caring for the well-respected Ruth Cuddlepot, she was no longer the organised and efficient educator I had been told she once was.
Ruth had, instead, evolved into ‘Ruthie’.
And thanks to the personality-morphing Alzheimer’s, Ruthie had become a frail, yet openly happy and affectionate elderly woman…. WHO LOVED TO HUG!
Even when her speech faltered, Ruthie could at least continue to communicate with a nice big welcoming embrace whenever I arrived for my shift. I looked forward to it in fact!
There she would be, perched in her favourite place on a big comfy chair in front of her enormous lounge room windows. The spot where she had the wonderful view of her ever-changing garden, the birds flying by to say hello… and where she could keep a watchful eye out for her next visitor whom she could throw her arms around and give a great big hearty squeeeeze to!
Really if it wasn’t so heart-breaking, it would be lovely.

– waiting for the next hug-ee!
Recently though, Ruthie had started calling me Wendy.
Which is fine by me, because you can imagine it happens a lot in this line of work (I’m also known as Debbie, Louise and Margie with some of my other cognitively-challenged clients). Let’s face it, remembering each of your carers’ name, rank and serial numbers is understandably not high on the priority list for some seniors.
Especially when they no longer know their OWN name!
I knew something had started to change in Ruthie when one day – the hugs stopped. And another cruel stage of the Alzheimer’s curse set in… Ruthie Cuddlepot started to become aggressive.
Without much warning her moods became erratic and it eventuated that Ruthie couldn’t STAND to be touched. Not even a handshake or a gentle pat on the shoulder. You just wouldn’t dare in case she would flare up and start screaming and punching the air (or anything else within proximity) in what appeared to be the ultimate frustration within Ruthie’s muddled-up mind.
This most heartless and indiscriminate Dementia had finally taken hold of her … it has been just awful to watch.
Finally, after accusations that Ruthie had started slapping and pushing her carers, we were told there was a serious incident last week where she had to be whisked away by ambulance and sedated in hospital.
Quite honestly, it became apparent to all, that they didn’t know WHAT to do with her!
After all Ruth’s organising, having purposely prepared herself and her future to remain forever being tended to in her own home by an army of paid care-working bees and service providers, it now seemed this was no longer a viable option.
I wonder now looking back, how Ruthie could have possibly planned for this final gloom-ridden phase of her illness?
Perhaps she’d anticipated that by this late phase: 1) she wouldn’t know where she was, and 2) she wouldn’t care? I hoped so for her sake.
The poem was right, and the best of Ruth had gone. And sadly yes, we had failed in standing beside her. Basically, it had become too unsafe to do so! Poor Ruthie had become a danger not only to herself, but to everyone else as well. And if a support worker is under any threat whilst looking after a client in in their home, then the people in charge needed to modify to an alternative arrangement.
I was informed only today that the once proud and brilliant Ruth Cuddlepot had been relocated ‘indefinitely’ into a High Care nursing home facility.
Just like the poem had foretold she was now sad and sick and lost. Her beautiful forward-thinking mind now full-to-capacity on sensory-depriving medication to keep her comatose and manageable (for her own protection, we were told).
I have deliberated greatly about going to visit Ruthie but honestly, what would be the point? And as harsh and as self-serving as might sound – I don’t think I could bear it.
The worst part is finding out she doesn’t even have a window.

HAPPY CARING!

I too worked in aged care (mental health) for some years. It is heartbreaking in the institutions when they are forgotten till gone, ANd then the vultures come out to squabble over the spoils! Saw that far too often.
So many Ruthies out there. We have been down this road so many times with friends and loved ones. Being with them one day at a time, one step at a time, taking joy in those moments of connection while they are still there is so important.
I wish there were more like you out there in the carers world.
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I’m so disappointed when ‘people’ are awful. Such a relief to discover that it’s not all of us!
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I couldn’t agree more. There have been some horrid stuff uncovered here by whistleblowers of late.
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Sadly the horrid stuff is as horrid as ever. Makes me feel sick each time another elder abuse case makes the news. Theres no excuses for these creeps!
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I know. I guess the more public exposure it gets the more likely it will be to stop. That’s the theory anyway
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Sadly my father died in April from Alzheimer’s he only had a short journey from diagnosis and my mum cared for him at home. I am also a person who has worked in care for 30 years and have experience of the different journeys people have. I now train and losing my dad has definitely made it hard to deliver dementia care training but I do with hope of giving just a little advice. Great blog
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Have just popped over to read your blog – you touch on so many topics and emotions, it’s a lovely read. Wow, 30 years working in Care… you must have seen it all by now. Funny though, how there’s still always the unexpected that comes along and makes you turn your head and say “WHAT THE..???”
Cheers Dollie.
PS: Sorry to hear about your Dad.
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Dear Dollie,
This is hard to write because I am writing to myself. My nickname is Dollie also. My husband has vascular dementia. They are times that I can hold my tears driving, at home, at work, and even when I am with him. They flow freely not even trying to get them to stop anymore. My husband is lost and I am too without him. Everyone tries to be understanding and give me space or evoke me in a hug. But it does not matter how much space or how many hugs it does not help. This cruel disease is hard for everyone.
much love,
Dollie
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