Categories
dementia care family reflexology Greif

Six Months On: A Birthday and Winster Wakes and remembering Dad

Six Months On: A Birthday and Winster Wakes and remembering Dad

           

People often say that time changes grief. I think that’s true, although perhaps not in the way I expected.

It has now been six months since Dad died, and life has carried on at its usual hectic pace. Sometimes it feels as though I have to deliberately make time and space to stop and think about Dad and how losing him has changed all of our lives.

Recently, our family went to plant more flowers on Dad’s grave. It gave me the chance to reflect on just how wonderful his funeral was.

Everything about the day felt so personal and so Dad. The flowers and the casket were filled with little details that reflected his life and the things he loved – boots, logs, a compass, a train, a jigsaw, boules, and so much more. Even now, the arrangement remains on his grave, which sits beside a footpath. Walkers staying at a nearby holiday cottage often stop to ask about it, and somehow that feels very fitting. Dad is still sparking conversations and stories.

One of the most emotional moments was Mum singing a song that Dad had requested many years ago. It tells the story of a folk singer who loved walking, but who reached the point where he could no longer “climb up them there mountains.” He wrote the song while sitting and waiting as his wife and sons carried on walking. Dad cried the first time he heard it, and it clearly stayed with him. Hearing Mum sing it at his funeral was incredibly moving.

The church was full, which meant so much to us. Thank you to everyone who came, to those who changed holiday plans, travelled long distances, watched online, and to the carers from Meadow View who joined us. Your kindness and support meant more than words can say.

We tried to capture every part of Dad’s life – from Morris dancing and the Guisers to boules and Onzain; from walking and Rangering to quiz nights; from life before Winster and everything that followed. Dad lived a wonderfully varied life, and that was reflected in the people who came and the stories they shared.

And there were so many stories.

Each one reminded us how many lives he touched, how much laughter he brought, and how deeply he was loved.

It was, of course, a sad day, but it was also a beautiful one. A day filled with love, music, memories, laughter and community.

A farewell Dad truly deserved.

Since then, we’ve reached two significant milestones: Dad’s first birthday without him, and our first Winster Wakes.

I’m not sure which was more emotional.

Dad’s birthday falls just after Winster Carnival, and this year I found myself stepping into his Witch’s shoes. I am so grateful to everyone who came to give me a hug over the weekend. Your kindness meant a great deal. I could also feel how much the whole village had been affected by the change in their village’s Witch. It made me incredibly proud to continue a tradition th

at Dad loved so much and to help keep Winster’s traditions alive.

For many years when we lived opposite the burton institute (winsters village hall), we held a birthday gathering on the Sunday after Carnival Saturday, finishing off anything left from the Winster Morris feast. Dad was usually in charge of buying the barrel of beer, and naturally it had to be finished over the weekend! I have many happy memories of Mum singing, Dad enjoying a pint, and putting the world to rights. The celebration of the end of Wakes went on late into the evening.  Then even later around our kitchen table. Those kitchen gatherings haven’t happened for many years (mainly because we moved house!) but it still filled my heart with sadness knowing that Dad would never again be part of another Wakes weekend.

A few days later came Dad’s birthday.

We visited his wildlife grave again and planted more flowers. His boots and little trains are still there, watching over him. Afterwards, Mum, my sister and I spent time talking about Dad.

This time, we didn’t tell the stories everyone had heard at the funeral. Instead, we remembered the everyday moments from the years he lived with dementia.

We talked about visiting him at Meadow View and the wonderful people who cared for him. We remembered the way he would sit smiling quietly to himself, perfectly content. We laughed about how, if he’d had enough tea, he would carefully tip it into someone else’s cup because he knew we’d encourage him to finish it if it stayed in his own. We remembered him proudly telling the staff that he liked three sugars in his tea, despite never taking sugar in his life. And we smiled at the memory of how he could dismantle absolutely anything—even toys that claimed to be indestructible.

Those are the moments I find myself missing now. The ordinary moments that became precious without us realising.

Life has carried on, and it is different now.

This blog will gradually return to being more focused on reflexology, but Dad will always be part of my story. I miss giving him reflexology, watching him look at me with those bright blue eyes, telling me that “it’s going up and down.” Those quiet moments together are memories I will always treasure.

Six months on, the grief hasn’t gone away—it has simply changed. It now sits alongside gratitude.

I feel incredibly privileged that he was my Dad.

Categories
dementia care family reflexology Greif

Six Months On: A Birthday and Winster Wakes and remembering Dad

Six Months On: A Birthday and Winster Wakes and remembering Dad

 

 

People often say that time changes grief. I think that’s true, although perhaps not in the way I expected.

It has now been six months since Dad died, and life has carried on at its usual hectic pace. Sometimes it feels as though I have to deliberately make time and space to stop and think about Dad and how losing him has changed all of our lives.

Recently, our family went to plant more flowers on Dad’s grave. It gave me the chance to reflect on just how wonderful his funeral was.

Everything about the day felt so personal and so Dad. The flowers and the casket were filled with little details that reflected his life and the things he loved – boots, logs, a compass, a train, a jigsaw, boules, and so much more. Even now, the arrangement remains on his grave, which sits beside a footpath. Walkers staying at a nearby holiday cottage often stop to ask about it, and somehow that feels very fitting. Dad is still sparking conversations and stories.

One of the most emotional moments was Mum singing a song that Dad had requested many years ago. It tells the story of a folk singer who loved walking, but who reached the point where he could no longer “climb up them there mountains.” He wrote the song while sitting and waiting as his wife and sons carried on walking. Dad cried the first time he heard it, and it clearly stayed with him. Hearing Mum sing it at his funeral was incredibly moving.

The church was full, which meant so much to us. Thank you to everyone who came, to those who changed holiday plans, travelled long distances, watched online, and to the carers from Meadow View who joined us. Your kindness and support meant more than words can say.

We tried to capture every part of Dad’s life – from Morris dancing and the Guisers to boules and Onzain; from walking and Rangering to quiz nights; from life before Winster and everything that followed. Dad lived a wonderfully varied life, and that was reflected in the people who came and the stories they shared.

And there were so many stories.

Each one reminded us how many lives he touched, how much laughter he brought, and how deeply he was loved.

It was, of course, a sad day, but it was also a beautiful one. A day filled with love, music, memories, laughter and community.

A farewell Dad truly deserved.

Since then, we’ve reached two significant milestones: Dad’s first birthday without him, and our first Winster Wakes.

I’m not sure which was more emotional.

Dad’s birthday falls just after Winster Carnival, and this year I found myself stepping into his Witch’s shoes. I am so grateful to everyone who came to give me a hug over the weekend. Your kindness meant a great deal. I could also feel how much the whole village had been affected by the change in their village’s Witch. It made me incredibly proud to continue a tradition that Dad loved so much and to help keep Winster’s traditions alive.

For many years when we lived opposite the burton institute (winsters village hall), we held a birthday gathering on the Sunday after Carnival Saturday, finishing off anything left from the Winster Morris feast. Dad was usually in charge of buying the barrel of beer, and naturally it had to be finished over the weekend! I have many happy memories of Mum singing, Dad enjoying a pint, and putting the world to rights. The celebration of the end of Wakes went on late into the evening.  Then even later around our kitchen table. Those kitchen gatherings haven’t happened for many years (mainly because we moved house!) but it still filled my heart with sadness knowing that Dad would never again be part of another Wakes weekend.

A few days later came Dad’s birthday.

We visited his wildlife grave again and planted more flowers. His boots and little trains are still there, watching over him. Afterwards, Mum, my sister and I spent time talking about Dad.

This time, we didn’t tell the stories everyone had heard at the funeral. Instead, we remembered the everyday moments from the years he lived with dementia.

We talked about visiting him at Meadow View and the wonderful people who cared for him. We remembered the way he would sit smiling quietly to himself, perfectly content. We laughed about how, if he’d had enough tea, he would carefully tip it into someone else’s cup because he knew we’d encourage him to finish it if it stayed in his own. We remembered him proudly telling the staff that he liked three sugars in his tea, despite never taking sugar in his life. And we smiled at the memory of how he could dismantle absolutely anything—even toys that claimed to be indestructible.

Those are the moments I find myself missing now. The ordinary moments that became precious without us realising.

Life has carried on, and it is different now.

This blog will gradually return to being more focused on reflexology, but Dad will always be part of my story. I miss giving him reflexology, watching him look at me with those bright blue eyes, telling me that “it’s going up and down.” Those quiet moments together are memories I will always treasure.

Six months on, the grief hasn’t gone away—it has simply changed. It now sits alongside gratitude.

I feel incredibly privileged that he was my Dad.

Categories
dementia care family reflexology Greif

31/1/26 Short blog post Dad’s last dementia adventure

Short blog post

Continuing Dad’s Story

After I published my last blog about Dad’s journey with vascular dementia, he died peacefully the following day. He was asleep, calm, and not alone — someone was holding his hand as he went. It was a gentle ending to a long and changing journey.

Dad’s funeral will take place on 9th February in his home village, a place that holds so many of his stories.

Although Dad is no longer physically with us, I don’t feel that this is the end of writing about him. I want to share how I used reflexology with him in his final months, and to write about his funeral — not just the day itself, but the memories, the stories, and the man behind them.

This blog will continue, as a wayof remembering, reflecting, and honouring Dad’s life.

Categories
dementia care family reflexology

18/1/26 Three Years at Meadow View: Watching My Dad Change

Three Years at Meadow View: Watching My Dad Change

When we could get out and about, cafe in Matlock

It will be three years in February since my dad moved into Meadow View Care Home. Three years sounds like a long time when you say it out loud, but in reality it has slipped past quietly, measured not in days or months, but in changes — some subtle, some heartbreaking, and some unexpectedly gentle.

 

Cup of tea with a favourite paper bag, well why not

The first two years that Dad was at Meadow View, his dementia was there, but more of Dad was present, but it hadn’t yet taken over the way it has now. Back then, I could still drive him home for visits. He could walk out of the care home beside me, wave to the staff, and confidently announce, “We are going this way now.” It was such a Dad thing to say — like he was still in charge, still leading the way, making sure everyone knew what was happening and that they were ok.

Those visits home feel very precious now.

I remember one time parking up outside the house, clipping the kerb slightly. Without missing a beat, Dad commented, exactly as any dad would: “If you have to hit it, it’s too close!” Dementia hadn’t touched that part of him yet — He always was a bad back seat driver.

How do you make a fire
Do we have to have a fire Dad its 26 degrees outside!

When we got home, there was always a routine. The very first thing he liked to do was check the wood store, choose a log, bring it inside, and sit watching the fire. There was something grounding about that — the familiarity, the quiet satisfaction of it. Even if it was in the middle of a heat wave, we still had to have a fire. Food was always important to Dad too, especially custard. One visit we had a custard tart, and as we were cutting it up he said happily, “This is going to be good.” It was such a small moment, but it stays with me.

Over time, those visits changed.

Here we go getting into the bus

We went from me driving Dad home, to him being brought to us in a wheelchair-adapted bus. From walking beside me, 

This is my private bus, not for you!

to sitting wrapped in blankets, movement now something to be managed rather than enjoyed. It can now take over 20 minutes to get him to stand up. Who knows if its because he doesn’t want to move, can’t work out how to move, or his knee is hurting him. mind you this is my Dad he could just be being obstinate. Dementia doesn’t announce these changes — they just arrive, one by one, until you realise how far things have shifted.

Meadow view café playing with magnates

Now, Dad talks much less. When he does, it’s often hard to know what he means. He might point outside and say, “It’s going around,” which clearly makes perfect sense to him, but leaves the rest of us guessing. One day, completely out of nowhere, he announced, “Did you just go clink clonk?” I have no idea where that came from. Sometimes all you can do is smile and let the words land where they land.

We will continue to bring him home when we can. He doesn’t like to move much now — his knee hurts, and really, why would you move if you’re comfortable where you are? He seems content. That matters more than anything.

If Mum sings to him, he brightens instantly, chuntering away happily, joining in in his own way. Occasionally, he comes out with a sentence that feels like a gift — something clear and perfectly placed, like “That’s my wife,” or “We are all here,” when the family are gathered around him. He also giggles to himself sometimes, as if he’s sharing a private joke with the world.

cup of tea at home

Those moments remind me that even though so much has changed, not everything is gone.

At the moment, this stage feels especially hard. Mum and I can’t visit him right now — I’m recovering from a hip operation, and Mum has dislocated her hip. Knowing he’s there without us physically being able to see him adds another layer of worry and guilt, even though we know it’s out of our control. Dementia already creates distance; being unable to cross that physical gap makes it feel heavier.

Meadow View has become a strange kind of constant in all of this. The staff know Dad’s routines, his comfort, his quiet ways. Trusting others with your parent is never easy, but over time I’ve learned that care, patience, and kindness can take many forms.

Dad seems content enough with his lot. And I think that’s what matters most.

As for me, I’m not sure how I feel about three years of him being in a home. Some days I feel acceptance, some days sadness, and some days a quiet disbelief that this is where we are. Loving someone with dementia means learning to live with unanswered questions — including how much time has passed, and how much more change is still to come.

Who knows what this year will bring.

For now, we hold onto the memories — the waved goodbyes, the kerbside advice, the firelight, the custard, the laughter — and 

 

we keep showing up, in whatever ways we can.