Some days I still forget he’s gone. I’ll catch myself thinking, I should tell Dad that, like he’s just on the other end of the phone. Dementia took him last year, but in truth, we lost parts of him long before. Watching someone you love slowly disappear—it messes with your head. He was funny, kind, hopeless at socks, and a DIY legend who made Sunday roasts like no one else. Even when his memory faded—when he forgot my name—our love stayed. That’s what I hold on to. He’s still my dad. Always will be.

Still My Dad

It’s weird. Some days I still forget he’s gone. I’ll be walking home from work or making a cup of tea and suddenly think, I should tell Dad about this. Like the time my mate Sam stacked it on his bike and landed in a bush—Dad would’ve loved that story. Proper belly laugh.

He passed away last year. Dementia. It started a few years before that, but honestly, we lost parts of him along the way. Watching someone you love slowly disappear like that… it messes with your head. Because they’re still there—but not really.

Dad was brilliant. One of those “can fix anything” kind of blokes. DIY legend. He once built a BBQ out of bricks in the garden and refused to buy a proper one, said it had more “character.” He’d wake up singing, wore awful socks on purpose to annoy my mum, and made the best Sunday roasts—Yorkshires like clouds.

We were close. He was a bit old-school, didn’t really do big emotions, but you always knew he cared. He taught me how to change a tyre, helped me move into my first flat, and when I was broke, he just slid a tenner into my hoodie pocket and pretended it wasn’t a big deal.

I first noticed something was off when he called me three times in one day to ask what time we were meeting for dinner. Same conversation. Every time. At first, I thought he was just stressed or tired. But then he got lost coming back from the supermarket—literally five minutes from our house. That scared me.

The diagnosis was rough. I went with him to the appointment. He kept cracking jokes—“Do I get a badge now?”—but I could see his hands shaking. When they said it was dementia, he just nodded, really slowly. Didn’t speak the whole car ride home.

After that, things changed fast. He stopped doing the crossword in the mornings, which really got to me. He’d always done it—used to tease me when I couldn’t get the clues. And conversations started to feel like broken records. He’d ask me the same question six times in ten minutes. I tried to stay patient, but I’d be lying if I said I didn’t snap sometimes. You feel guilty straight away, of course. But you’re only human.

One of the hardest bits? When he forgot my name. Called me “the young lad” a few times. That broke me. It’s not just the memory loss—it’s like little pieces of their personality go missing. He got scared a lot. Paranoid. Thought people were stealing from him. He’d never been like that.

But there were good days too. Like when I played him an old Oasis song and he suddenly lit up, started singing along. Or when we watched the footy and he somehow still remembered all the chants. We’d eat chips, shout at the telly—it felt normal for a bit. I lived for those moments.

Mum struggled. She never said it, but you could see it on her face. Exhausted. Heartbroken. My sister and I took shifts, gave her space when we could. We started leaving notes around the house for Dad—like, “Milk’s in the fridge” or “You’ve already had lunch.” Little things that helped.

We also had this routine—every Saturday morning, we’d walk around the block with him. He’d forget halfway through why we were walking, but he liked it. And it gave us something to hold onto.

The carers were legends. Absolute saints. They treated him with dignity, even when he was having a bad day. I don’t think people realise how much difference that makes—not just to the person with dementia, but to the whole family.

If I had to give advice to anyone else going through this, I’d say: be kind to yourself. You’re going to mess up. You’ll get frustrated. You’ll cry when you least expect it—like in Tesco, next to the cereal aisle. That happened to me. Something about seeing his favourite cornflakes.

I miss him every day. I miss his daft jokes, the way he’d whistle like a kettle when he snored, even the way he’d tell the same story over and over again. I wish I’d recorded his laugh. I wish I’d told him more often how much I loved him before the words stopped meaning anything to him.

But I know he knew. Somewhere deep down, he knew.

Dementia is brutal. It steals things in slow motion. But it doesn’t touch love. That sticks. Even when everything else fades.

He’s still my dad. Always will be.

share this story:

Facebook
Twitter
LinkedIn
WhatsApp
Email

More stories

Biddy—real name Frances, but always Biddy to us—still has that beautiful smile and spark, even as dementia slowly changes things. The diagnosis didn’t come as a shock; the changes crept in so gradually they just became part of life. These days, we take things at a gentler pace—walks, bus rides, singing old classics at Singing for Memory. If there’s one thing I’ve learned, it’s not to dwell. Keep it light, keep it moving, and hold onto the moments that still shine through.

Read More

I’m Marco, and I’ve been living with dementia for nearly ten years. It started gradually—forgotten names, missed appointments—but slowly, it became impossible to ignore. Since then, life’s changed, but I’m still here. I still garden, play word games, go to the memory café, and spend time with my family—who mean everything to me. Some days are tough, especially when I can’t support my wife like I used to or find the right words. But I try to hold on to who I am. Dementia takes a lot, but it hasn’t taken my love for life. Not yet.

Read More

It’s been ten years of sensing changes without a proper diagnosis—ten years of living in a strange in-between. We all know it’s there. We feel it. But getting someone official to confirm it? That part still hasn’t happened. Life has shifted quietly around us. Some days, it feels like standing in the middle of a slow, unstoppable drift—watching someone you love change, bit by bit. No big moments, no loud alarms. Just a stillness growing where there used to be energy, laughter replaced by tired smiles. And through it all, we’re still here, doing the best we can.

Read More

Howard Hopkins was an incredible man—determined, clever, and full of life. Together, we built a life rich with adventure and simple joys. But dementia still found him. I noticed the signs before we had a diagnosis—small things you only piece together in hindsight. Caring for him became my life’s rhythm: finding creative ways to ease his confusion, holding onto the man I loved even as pieces of him slipped away. Dementia taught me that love isn’t just about memories; it’s about presence. You can’t fight it by saying no—you adapt, you find another way, and you never, ever do it alone.

Read More

Dementia has taken much from us — conversation, spontaneity, the easy rhythms of daily life. Yet through it all, Gerald’s kindness remains. In the smallest routines, in the quiet moments we share, I find the shape of our love still holding strong.

Read More

John was always a gentle, dependable man. Dementia crept into our lives slowly, stealing little pieces of him at a time. Where conversation once flowed, now there is silence; where independence once stood, now there is quiet reliance. Yet even as the disease has taken so much, it has not touched the deeper parts of him — the part that, for a time, could still pray with clarity even when everyday words escaped him. Love remains between us, reshaped but enduring, carried in small routines, shared glances, and simple acts of care. This journey has taught me patience, resilience, and a tenderness I never knew I would need.

Read More
Receive the latest news

Subscribe To Our Newsletter

Exhibitions. Project Updates. Stories. Plus More.