Trevor with his wife Yvonne

My wife’s person-centred care has improved her life with dementia, and mine

Trevor Salomon and his wife Yvonne have seen many changes since her dementia diagnosis in 2013. While Yvonne’s move to a care home in 2019 was a difficult decision, Trevor explains how the staff have made it feel like a home from home.

Before her diagnosis, my wife Yvonne astonished everyone with her ability to do anything she set her mind to.

She was an amazing cook and hostess, and our house was always full of family and friends. She loved gardening and especially weeding the borders, taking pride in immaculate flower beds. There was little or nothing she couldn’t make or repair on her sewing machine. 

Early signs and adjustment

Yvonne used to happily go off to work as a bookkeeper for a local charity. She would often bring home files and documentation so that she never missed a deadline.

In 2009, the first signs of dementia manifested themselves in short term memory loss and constant repetition.

Although not diagnosed at this stage, she realised she could no longer cope with numbers and spreadsheets. Yvonne applied for a job as an online picker at Sainsbury’s and started her role there in the summer of 2012.

Switching roles

It was 2013 when we finally received confirmation of young onset Alzheimer’s. By that point, Yvonne's capabilities had dramatically declined so we simply switched roles. She became my sous chef and I took over most of the gardening. I confess, though, that I never did get my head around sewing and interlock machines.

Trevor, Yvonne and family in the garden

Trevor, Yvonne and family

Sainsbury’s astounded our family by keeping Yvonne employed for a further four years. The company found ways to constantly make her job easier and reduce her work hours. They explained to her colleagues the need to look out for her and how best to support her. 

‘I have no doubt that having meaning to her days kept Yvonne’s brain stimulated and helped to stave off the rapid decline.’

This lasted until, unable to find her way either in or out of the store, she eventually had to give up her job in early 2018.

Considering care options

Yvonne and I had wonderful support from family and friends alike. We also used the services of a day centre a couple of days a week, as well as enjoying Singing for the Brain sessions. However, I eventually realised that I was burning out. 

The tipping point for me came with the onset of Yvonne’s double incontinence. At this time, towards the end of 2018, I realised I could no longer recharge my batteries and needed to consider professional care.

I looked at three options: carers coming to our house at given times of the day, live-in carers and finally full-time residential care in a specialist dementia home. 

My kids and Yvonne’s sister were very supportive of Yvonne receiving the best care possible whilst also allowing me to lead a life. I had not been able to do so for a very long time, and with this in mind I focussed solely on the care home option.

The main decision criteria for me were consistency of care and a person-centric approach. 

‘It was important that any care home recognised Yvonne’s age and interests.’

Yvonne in the garden smiling

Trevor began to consider care options for Yvonne in 2018

Above all, I wanted an environment that would be the antithesis of the depressing care homes I remember visiting as a child to see aging relatives.

I invested three months in evaluating six care homes. We were lucky to find somewhere less than 20 minutes from where we lived which met all my criteria.

A home from home

From day one, in May 2019, Yvonne loved the home. She never once asked why she was there or why she wasn’t leaving with me after a visit. I hope this proves that, fortuitously, we got the timing spot-on, and I made the right decision.

‘Knowing Yvonne’s interests, the care home staff are mindful of which activities she finds most stimulating.’

Two photos of Yvonne in the care home; smiling and petting a cat

Yvonne moved to a care home in May 2019 and has settled in well

They have made a point of spending 1:1 time with her in the garden. The staff support Yvonne to fill the bird feeders, do simple gardening and pick tomatoes in the mini greenhouse. They also help her with biscuit baking using her favourite simple recipes, which I take in for them to buy the ingredients and use. 

For Yvonne this must have felt like home from home and was beyond doubt one of the reasons she settled in so well.

I could write at length about the last two years of coronavirus and how that has impacted Yvonne, as well as the wonderful staff at the home. But that’s a blog in its own right.

I’ll close by answering a question that I’ve been asked by many on many occasions. Do I feel guilty about having Yvonne cared for outside of our family home? The answer is a simple and definite ‘no’ because I know I would have felt guilty soldiering on when I was exhausted and ultimately not doing my best for her.

Making social care work for people with dementia

The All-Party Parliamentary Group on Dementia is conducting an inquiry into how the social care workforce can support people with dementia to live the lives they wish to lead. 

Find out more

113 comments

Beautifully written Trevor.

Thank you, Julie x

What a wonderful piece and hopefully will be very helpful to others struggling with these decisions. Tapping into the person’s interests is absolutely crucial and I’m so glad Yvonne’s time is spent doing what she loves instead of just vegetating. Proof that with the right support, people can live well with dementia.

Thank you for your comments, Clare. Believe me, I did visit and assess care homes where I left unconvinced that residents would be stimulated. In this respect the lovely thing about Yvonne's care home is that they have an activities team who are as much focussed on the unique needs of each resident as they are on common interests, something I hugely appreciate.

What a wonderful account of how this dreadful disease should be treated. It is very obvious of the love and care went into decisions that had to be made. So lovely to hear how family and friends can all come together at such a difficult time. You wrote a very heartwarming account.

Thank you so much for your kind comments, Dawn. Two words I always took on board from Alzheimer's Society were 'disclose' and 'embrace'............disclose the diagnosis as soon as it's known and don't hide behind it, and embrace all offers of support because it's going to be needed.

Trevor you showed your strength and love by putting Yvonne’s needs above all else. I can imagine the soul searching you put yourself through. You did the kindest thing possible and ensured you both have a quality of life. Thank you for sharing Yvonne’s story. Young dementia is extremely sad and difficult to understand. It wax good to learn her employer and staff made it possible for you all to cling onto some sort of normality

Thanks so much, Lesley. Everyone around us was wonderful from day 1 of Yvonne's diagnosis. It's the bureaucracy and mind numbing challenging processes where the angst kicks in. I can't even begin to explain how stressful it is to try and find one's way through the benefits system, support entitlement etc etc. I'm lucky in the sense that I don't ever roll over and give up but for many families this is a real nightmare.

I am so glad a good home was found for Yvonne and I know there are wonderful places out there. We hear about the ones that don'f do so well (according to the QCQ anyway) so it is good to hear about a wonderful one. if I get dementia I would want my daughter to find a place like that for me

Hello Moira. Thanks for your feedback. I was once asked what would be my worst nightmare if I needed to be cared for in a home. The answer I gave was that it would freak me out if I found myself sitting in a circle in some soulless gloomy room, singing songs from the First World War !

Reading this, it's obvious that you have dealt with the issues in the best possible way, after deep consideration, The options that you chose were absolutely spot on, and I think (while I am far from objective) that the blog is inspiring, and extremely well written. Thank you!

My wife Lucie was finally ,diagnosed in 2019, as suffering from mixed dimentia,due to vascular ischemia,affecting subcortical (may also be frontal lobe) region of the brain. we both are 80 years old.
Lucie's caring is primarily by our mutual love for each other,which goes back 55 years and changing Carers, supplied by different care agencies.
In short Lucie is.happy with love, compassion and empathy. We don't see any other alternatives but staying at home, as care home is vvvv expensive, i.e 4000 pound per month, with varying reviews.Nevertheless,I am still on the lookout,
We don't qualify for support from government, though Lucie gets bisma pension, as she worked voluntarily. Reading this I feel inspired, hope I get tefered to a good and affordable care home or v.goox care agency with less mindful to making money at the expence of sufferers
Hope government is listening to the silent,cry from these sufferers,longing for living with dignity ,love and empathy.

Hello Pranab. I was touched by your love for Lucie and everything you do for her. I am a very practical person and so my biggest fear was always that something might happen to me (a bad fall, need to go into hospital etc) and thus it would impact Yvonne. May I therefore respectfully suggest that you have a plan B for Lucie in such an eventuality and that this plan is written down and shared with your family/best friends.........whoever would be acting on your behalf. So few carers do this but none of us knows what is around the proverbial corner. My best wishes to you.

Thank you Howie !

Excellently written article. Trevor is my best pal and I know that everything he has written is heartfelt, true and accurate. He has selflessly done everything he can for Yvonne to ensure that she remains the happiest she can be in tragic circumstances. He is quite simply a wonderful husband, father and human being.

Thank you so much, Mr Ben x