Lucy’s story: ‘Since Dad was diagnosed I have felt pretty much every emotion going’

After her dad received a diagnosis of mixed dementia, Lucy Parkes has felt a confusing range of emotions. Read how she’s learning to accept their ever-changing relationship.

Firstly, let me tell you a little bit about me and Dad.

I am 30 and my dad, Roger, is 81. Our story began nearly three years ago when I noticed Dad was becoming forgetful and confused more frequently.

Dad lives alone and it became clear he was struggling to care for himself. He would go out late at night and not understand why all the shops were closed. He stopped showering and would often be wearing dirty clothes. Incontinence became a problem too.

I took him to see his GP and from there it took a long, 18 months to get the diagnosis. It was only after an MRI that, last September, we were told that Dad had Vascular dementia and Alzheimer’s in the moderate stages.

Lucy and her dad, Roger

Lucy as a baby pictured with her dad, Roger.

Getting prepared, getting practical

Initially, the news brought a sense of relief. Now we know what is wrong with him we can focus on a cure. Surely dementia is just when old people become forgetful, right?

Unfortunately this is not the case. The doctor gently told us the prognosis. Vascular dementia was incurable. His symptoms would worsen. His memory would deteriorate and his cognitive function would decline. We needed to prepare ourselves for the inevitable and the support and care that he would now need.

There is great emphasis on the practical support needed by people living with dementia and their families. This is true, the support is greatly needed as routine tasks – washing, dressing, meal prep – become harder and then impossible to do. But as well as these practical challenges, what about the emotional side of the disease?

Feeling the impact

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It has now been a year since Dad’s diagnosis and I have felt pretty much every emotion going. Sadness, obviously, especially in the immediate period after the diagnosis when I would switch between feeling ‘fine’ to crying in the supermarket because they were out of avocados (I soon realised that I’m definitely not crying because of the avocados!).

I have felt confusion. Dementia is so complex and every day is different. Dad can be perfectly clear and lucid one day and then have no grasp of what is going on the next.

There has been a lot of ‘first times’ for us all. The first time Dad asked when he could go and visit his mom, who passed away nearly 30 years ago. The first time Dad confidently told me that he had been on a boat to Bristol, when I knew he had not left the comfort of his sofa. What did I say about this being a complex disease?

I have also felt self-pity. Why him? Why us? I would be lying if I said I have not felt anger and resentment towards my Dad at times too.

These feelings are quickly followed by guilt, which can become overwhelming. I feel guilty for not being more patient, for not spending enough time with him, for not doing more. I even feel guilty for those times I don’t feel guilty.

Good times and bad

I would like to stress that it is not all doom and gloom. There are still nice times. Times of love, affection, and humour too. Dad can say some pretty out there things, (note the boat trip to Bristol,) and you have to laugh, because if you do not laugh you will cry. We have done too much of that already.

So, one year on from the diagnosis, I have learned to just accept. There are going to be good times and there are going to be bad times and I am going to feel a range of emotions. Who would not?

We are still father and daughter but our relationship is different now. I guess the inevitable has happened and the roles have reversed. Dad has changed, but he is still Dad and always will be. He is just going to be a new version of Dad and I need to accept that.

At the end of the day the only thing constant in life is change.

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I’m very sad as my lovely dad today received a diagnosis of mixed dementia. My mum and dad are in their 80s and have been married for 60 years so she’s taken it hard. He has suffered several mini strokes. He experiences a lot of deja vu and short term memory loss. We are still in the early stages and medication is being prescribed to help delay the progression. He is a wonderful man and will always be my dad no matter what the future brings. We will love and care for him come what may.

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Hello Kathryn,

Thanks for getting in touch. We're really sorry to hear about your dad's recent diagnosis. This must be such a worrying time for you and your family.

If you've any questions, we recommend speaking with one of our friendly advisers on 0333 150 3456. They will listen to the situation regarding your parents, and provide information, support and advice:

You may also benefit from talking with other people who have been - or are currently going through - a similar situation to you. Our online community, Talking Point, is a place for people and families affected by dementia to share their experiences and provide peer support:…

In the meantime, we do have further information about mixed dementia, in case you haven't already seen it:

We hope this is helpful, Kathryn.

Alzheimer's Society blog team

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Hi , My Dad has mixed dementia..he was diagnosed in August 2018..6 days after diagnosis..he developed sepsis, & bowel obstruction..Dad was on end of life care..we were heartbroken...however he made a massive recovery.. unbelievable..Dad is in a care home, because Mam cannot manage him at home..Dad is there sometimes, but other days he isn' so hard & Dad doesn't really know what's up with him..He also has recurring lymphoma..just so hard..

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My Dad is in the early stages of alzheimers and vascular dementia. He is a little bit forgetful and confused at times but seems OK. What should I look out for please. Never experienced this before. Thank you.

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Hello, thank you for your message. It can feel overwhelming when someone close has a diagnosis of dementia. I can hear how useful a local contact would be in supporting both yourself and your dad. Local Alzheimer’s Society can offer support through Dementia support workers or advisers in certain areas, please click on the following link:

You mention that your dad is a little bit forgetful and confused at times. It may be an idea to find out how your dad feels and what support he may find useful at this stage. The dementia guide: and the Memory handbook: are useful to look at together when someone has received a diagnosis.

Alzheimer’s and vascular dementia is the most common type of mixed dementia. Often someone will have a greater amount of one type of dementia than another. You can find further information on the different symptoms at the following link:

I do hope this has been of some guidance; if you would like to, please do get in touch with the helpline to speak to an adviser at the following link:

Best regards, Helpline team (Alzheimer's Society)

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My dad had the same illness, and I know exactly how you are feeling . Keep strong as a family , and take every day as it comes . My dad changed so much so it was hard him and also hard for us . Sending love to you ❤️

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Sending love to you and your Dad thanks for the humour.
My Mum is 3 years in with the same diagnosis. We have had many first times too. Like the time she saw Princess Diana on the high street and the time she was convinced a famous actor was her boyfriend. You do have to laugh but I feel your pain too. Hoping for more good days than bad for you x

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My dad has Vascular dementia. Hes now in a home as I work full time and it was too much for mum. He would sleep all day and not settle at night wanting to go home - even though he was already home. Its hard putting him in a home but dad is settled mum is no longer scared in her home and I feel guilty every day that I couldnt look after him.

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Thank you for sharing your story. I recently lost my dad at 80, after an 8 year battle with Dementia with Lewy Bodies. I’m 28, so I feel like I never really got to know him as an adult because I was too busy growing out of my obnoxious adolescent phase when he was diagnosed. There are so many emotions we experience as caregivers throughout the course of the disease, guilt, regret, anger and loneliness have played the biggest parts for me. Well done for being strong and sharing your story, to remind the rest of us that we’re not alone.

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At the end of the day the only constant thing in life is change. I told my daughter that the other night. Xxxx. We found out 2 month ago my mum has mixed dementia and ur story gave me a little atrength. Xx good luck to you and your dad

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