Week 3 of our Course – Adapting and Relationships…….

Yesterday saw me trundling early doors into York for the 3rd session of our Good Life with Dementia Course.

On Friday I met 3 lovely sisters in York; one who lived there, one over from Canada and the third, diagnosed in February, who was over from her home in France. They’d asked via email if I’d meet them in York for a cuppa and a chat. They were wonderful people, all doing their best to come to terms with a diagnosis and finding ways of understanding . I invited them along to Tuesdays session but sadly, Sue was on an early flight back to France that very morning. I was the first person with dementia she’d actually met in person as they don’t have groups like Minds and Voices in her part of the country and internet connection is very poor so I left them feeling very fortunate and lucky to have all my virtual playmates as well as in reality.

No one should be alone with dementia……..😔

Anyway, back to the fortunate me and I got up to a rainy day which definitely had an autumnal feel to it, but by the time the taxi got to the bus station, the sky was looking promising for the day ahead

Week 3 of our course was all around Adapting and Relationships. Me and Damian had talked about the flatness of last week and were both determined to make up for it this week.

It suddenly occurred to me that Damian went to set up and then came to pick me up from the station, so yestretrday we got our act together and he picked me up at 9am so I helped or hindered him to set up!

I went a different way to the station today and so got a different river view

But then must have taken a wrong turn and everything looked wrong…..lots of road works and noise…..so I was in a bit of a pickle, not knowing where I was……but I didn’t panic, I just followed the river and knew I’d come out somewhere close….and I did…….AND breathe……..

Damian picked me up and we set everything up before people arrived.

Tutor this week were me Eddy, Brian, Eric, Elaine and Brian…….

Everyone started to arrive and chat and laugh and catch up………❤️

We all went round and said our names again and then I started off the conversation about the importance of the person and those around them. When we get the diagnosis so do those around us and both parties need help and support from the beginning and that’s what missing in the diagnosis process. If the beginning is a confused mess, the mess will become more tangled……….I spoke about the advantage I see in living alone as there’s no one to move things around……to which Elaine piped up

Eric never moves things cos he never dusts!” ………🤣

It’s difficult to know what things not to do” said a partner

That has been something for us that has been very difficult for us” said a learner……”Readjusting to new roles and abilities……is so difficult”

The changing roles, when someone who has always, for example, done the driving, now suddenly can’t………”It’s demolishing a lot of what we’ve always done..” so it’s hard both ways

It’s not life threatening so I just get on with it”…….said our learner who lives alone…..

The whole aspect of your life as a couple changes, it’s a huge learning curve’

We do more things together now and it makes you think you have to make time to do those things and turning it into a positive instead of a negative……”

“Technology is making life difficult for me – I can’t do everything online,

“I get on as best I can as I don’t have any technology’………

People shouldn’t be disadvantaged simply because they don’t have or use technology……their comments put a new perspective on technology….

Such great discussion on issues suddenly arising that were never thought of or mentioned at diagnosis, people simply don’t know how to deal with it…….if all this was dealt with at diagnosis, how easier the transisition would be……

We watched Damian’s ‘Getting Along short 5 minute film, where couples explain the issues and talk….people with dementia don’t want to be defined by their dementia and carers don’t want to be defined by that title either – they’re husband and wife……..frustration and lack of knowledge impacted on relationships. So important to challenge misconceptions, to talk and give those in relationships the chance to talk through problems without it causing friction……

When you’ve lived with someone for 50 years, and done things the same way, it’s hard to adapt” said Eddys wife on the film…….

Damian said he met many couples “Falling into traps that dementia sets and tearing couples apart” and this is why he created the ‘Getting along’ sessions. Identity is often lost or changed when dementia arrives.

The partners can often look into the future and see a totally different world to what they were hoping for and go into denial and sometimes the person with dementia goes into denial simply through fear.

The demands of the house, and just everyday living comes into question”…my wife has found it difficult to come to terms with……

I said ‘ If services were suddenly to fill the gaps that are missing, it would cost billions in their eyes  as so much is missing, but if they looked at services differently they would see that the cost of referring to our course, for example, is cheaper than anything they could provide and nowhere near as beneficial”

“No one asks you how are you coping with the dementia” whereas if you’re diagnosed with cancer, everything is put into place for those that want it, support, counselling, it’s all covered ………dementia is forgotten in the grand scheme of things….

Tea break but the chatter continued non stop in small groups…..wonderful!

Those of us who are single said it was great as we don’t argue with ourselves, we don’t have the guilt and we can do what we want without being criticised.

I’m always saying sorry to my hubby” said Elaine

Paul always said  he’s been happily married for 10 years which is not bad after 56 years……😂🤣”

“Marriage is like a pack of cards, you start off with hearts and diamonds and end with clubs and spades…”🤣😂 all the one liners came out…..

Once you’ve accepted it you can do something about it, but it must be hard for those in denial, or don’t accept there could be

We asked what annoys you about the way people interact with you

Being patronised……

People saying ‘don’t you remember’?

‘You don’t look like you have dementia’

“Ive just been talking to him in the pub, he can’t have dementia’

Before we had a round up I spoke about not forgetting the children in all this as if they’re not included they’ll make up their own idea of what’s going on which might be far from the truth.

We went round the room to finish off and asked the learners what they were taking away…

Better for coming here”

“Nice to have everyone’s views’

It’s an opportunity to talk about things you often hide inside your head”

And in the blink of an eye, the 2 hours were up and I can’t believe I let the tutors all disappear without a piccie. But I managed to Eddy and me and Simon, as it was his last day with us before flying back to Belgium…

Last we we went a bit flat….whereas this week we got back on track and we had wonderful conversations……….everyone was animated and willing to share their experiences, good and bad and everyone seemed to feel better for doing that……..

It’s always exhausting yet exhilarating doing our course so I often fall asleep on the bus home…..but with views like this…..it’s no surprise as it’s a very calming trundle home

About wendy7713

On the 31st July 2014 I was diagnosed with Young Onset Dementia. I may not have much of a short term memory anymore but that date is one I’ll never forget. I’m 58 years young, live happily alone in Yorkshire, have 2 daughters and I’m currently still in full time employment in the NHS. However, I’m now in the process of taking early retirement to give me a chance of enjoying life while I’m still me. I've started this blog to allow me, in the first instance, to write all my thoughts before they’re lost. If anyone chooses to follow my ramblings it will serve as a way of raising awareness on the lack of research into Alzheimer's. It will hopefully convey the helplessness of those diagnosed with dementia, as there is no cure – the end is inevitable. However, I’m also hoping I can convey that, although we've been diagnosed, people like me still have a substantial contribution to make; we still have a sense of humour; we sill have feelings. I’m hoping to show the reality of trying to cope on a day to day basis with the ever-changing environment that dementia throws at those diagnosed with the condition. What I want is not sympathy. What I want is simply to raise awareness.

8 thoughts on “Week 3 of our Course – Adapting and Relationships…….

  1. Wendy, you are so inspirational. I have been following your blog since I read your book. My late mother had early onset Alzheimers. I would have loved to have my mother living with us, after my stepfather died. However she insisted on living in her flat with full time care, said she did not want to be a burden. Your writing has explained so much. Thank you Linda P

    Liked by 1 person

  2. One of the issues which have arisen is lots of bills, insurance, Council tax etc are in my husband’s name so they don’t like speaking to me. As he can hardly remember his name or date of birth and doesn’t know the address it’s tricky. Apart from that he doesn’t like speaking on the phone. So remind everyone to get powers of attorney as I think I’ll now need them more than ever.

    Liked by 1 person

  3. Wendy this sounds so wonderful, with so much learning, and happiness and laughter. It’s a lovely read, with fantastic photos to gaze at! Thank you once again!

    Liked by 1 person

  4. Hi Wendy. I am an Occuaptional Therapist working with individuals who have received a diagnosis of young onset dementia and would really like to hear more about your Good life with Dementia course! Sarah

    Liked by 1 person

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