top of page

Managing the Changing Landscape: Sensory Overload, Slipping Words, and Finding the Strength to Keep Moving Forward.


Meeting the Challenge of decline
Meeting the Challenge of decline

Living with young-onset Alzheimer’s disease has meant becoming an expert in a landscape that refuses to stay still. For a long time, I’ve mapped out my routines, found my workarounds, and established a feeling of control over my daily life. I tell myself that I know what to expect. But the reality of a progressive condition is that it is always moving, always reshaping the extent of what you can comfortably do.


Lately, I’ve been noticing a shift. It is a quiet, persistent deterioration in my condition, a subtle sharpening of the challenges I face every day. It’s making itself known not in dramatic moments, but in the ordinary spaces of daily life, particularly when I try to navigate large public spaces or simply try to hold a conversation at the end of a long day.


Admitting that things are getting harder is never easy. There is always a temptation to brush it under the carpet, to blame a bad day on poor sleep, or to pretend that a momentary lapse was just a normal bit of forgetfulness. But honesty is the only way to manage this journey with dignity. The truth is, my brain is changing, and with those changes comes a completely new relationship with the world that surrounds me.


Two areas in particular have become increasingly difficult to manage: the intense sensory overload of large public environments like supermarkets, and the frustrating way my speech begins to break down when I’m tired.


Out and About

There was a time when a trip to a large supermarket was a completely mindless chore. I grabbed a trolley, walked down the aisles, picked up what I needed, checked out, and left. I did it without a second thought. But lately, these vast, bustling spaces have changed into something entirely different. They have become overwhelming, disorienting, and incredibly difficult to tolerate.


When you have Alzheimer’s, your brain loses its ability to filter out background noise and visual clutter. A healthy brain does a magnificent job of sorting through information, deciding what is important, and disregarding the rest. It tunes out the whirr of the refrigeration units, the chatter of people two aisles over, the bright glare of the overhead fluorescent tubes, and the dizzying array of brightly coloured packaging lining the shelves.

For me, that filter is wearing thin.


Walking into a large supermarket now feels as if stepping directly into a wall of sensory input. Everything arrives at once, at maximum volume, and my brain wrestles to process it.

The Auditory Assault: The noise is relentless. It's not just loud; it's chaotic. There's the rattle of trollies, the beep-beep-beep of the barcode scanners at the checkouts, the heavy pulsation of the air conditioning, the scraping of stock cages on the floor, and the announcements blaring overhead.


Because my brain cannot categorise these noises and push them to the background, I hear all of them with equal intensity. It creates a noisy, chaotic wall of sound that makes it incredibly hard to focus on a simple task, like remembering why I walked down a particular aisle in the first place.


Visually, a supermarket is a maze of distractions. The lighting is intensely bright, reflecting off polished floors and plastic packaging. Then there are the choices. An entire aisle dedicated to cereal or coffee sounds like a triumph of modern consumerism, but to a brain dealing with cognitive decline, it's an absolute nightmare. Looking at dozens of different boxes, trying to read small text, and trying to distinguish between brands becomes an exhausting exercise. The rows of shelves begin to blur together, and the perspective of the long aisles can feel strangely distorted.


The sheer scale of these public spaces makes navigation a challenge. If I lose my bearings for even a moment, a sudden wave of disorientation can hit me. I might look around and realise I have no idea which direction the front of the shop is, or how to get back to a familiar point. It feels like being trapped in a maze where the walls are constantly shifting - It frightens me.


Such sensory overload isn’t just unpleasant; it’s physically and mentally draining. It saps my energy within minutes. I can feel a physical tension building up in my shoulders, a rising sense of anxiety, and a powerful urge to simply abandon the trolley and find the exit.


What used to be a routine thirty-minute errand now requires the tactical planning of a military operation, and even then, it leaves me utterly exhausted for hours afterwards.


When the Mind Trims the Details: The Challenge of Public Spaces

It’s not just supermarkets, either. This difficulty extends to almost any large, unstructured public space. High streets, train stations, busy libraries, and community hubs all present the same series of obstacles.

The common denominator is unpredictability and movement.

In a quiet, familiar environment, like my own home, my brain knows the layout perfectly. Everything has a place, the lighting is consistent, and there are no unexpected surprises. I can manage my symptoms well because the environment stays static. But public spaces are dynamic. People walk at different speeds, cross in front of you unexpectedly, stop suddenly to look at their phones, or call out to friends.


When you’re working to navigate a crowded pavement or a busy station concourse, your brain has to constantly calculate distances, predict the movements of others, and adjust your own footsteps accordingly. For me, those calculations take much longer now. I find myself stopping dead in my tracks because I can’t quite figure out which way a person approaching me is going to step. It can make me feel clumsy, conspicuous, and vulnerable.


Because of this, I find myself retreating slightly from these environments. I look for quieter times to venture out, seek out smaller independent shops where the tempo is gentler, and rely more heavily on familiar routes. It’s a necessary adaptation, but it’s also a strong reminder of how the world is gradually shrinking at the edges.


Here's an infographic I made to try and explain the cycle of the sensory overload I experience:



Fatigue and the Slipping of Speech

The second area where I’m noticing a clear deterioration is in my speech, specifically how it correlates with fatigue.


Living with Alzheimer’s means that my brain is working on overdrive just to perform standard tasks. It’s running a marathon every single day, trying to find alternative neural pathways to bypass the damaged areas. By the time late afternoon or evening rolls around, my cognitive battery is flat. That’s when the cracks begin to show, particularly in conversation.


When I’m tired, my ability to find the right words starts to slip away in a very specific, frustrating way. It’s a disorder known as anomia, or word-finding difficulty (I’ve done my research!), but experiencing it feels much more personal than a medical term, It’s a strange, jarring sensation.


In my mind, the concept of what I want to say is perfectly clear. If I’m thinking about a round, orange fruit that you peel, the mental image is vivid. I know what it tastes like, I know what it looks like, and I know exactly what I want. But when the signal travels from my brain to my mouth, something goes wrong in the translation.


Instead of saying “orange,” my tongue will confidently pronounce “apple.” “Could you pass me that apple?” I I’ll ask, while pointing directly at the fruit bowl. To the person I’m talking to, it sounds like a bizarre mistake or a strange joke. To me, the moment the word leaves my lips, I often realise it’s wrong, but I can’t immediately find the correct one to replace it.


Other times, I’m completely unaware that I have used the wrong word until I see a look of confusion cross someone’s face. This misnaming usually follows a certain logic. I rarely substitute a word with something completely unrelated, like calling a car a shoe. Instead, my brain pulls a word from the same category or family.


Fruit for fruit: Apple instead of orange.

Vehicle for vehicle: Train instead of bus.

Furniture for furniture: Chair instead of table.


It's as if my brain can find the right drawer in the filing cabinet, but it grabs the wrong folder! This makes conversation incredibly tiring. When you’re in a lively, fast-paced discussion with friends or family, sentences fly back and forth quickly. When you have to constantly pause, search for a word, correct a mistake, or explain around a missing word, you quickly fall behind the rhythm of the conversation.


You become a spectator in a room where you used to be a participant. It requires a massive amount of mental effort to stay engaged. I have to think about every individual sentence before I say it, checking the words for correctness before letting them out. When you’re already tired, that extra layer of effort is exhausting. It’s often easier to just stay quiet, to nod along, and to let others do the talking. It’s a lonely feeling, sitting in a room full of people you love, wanting to contribute, but feeling locked behind a barrier of slipping words.


Adapting to the New Reality.

It would be very easy to look at these changes and feel despair. It’s disheartening to watch things that used to be second nature become major hurdles. But if there is one thing this journey has demonstrated to me, it is that dwelling on what has been lost doesn’t help you navigate what remains.


These problems, as frustrating and exhausting as they are, are only to be expected. Alzheimer’s is a progressive disease; it’s the nature of the beast. Expecting my brain to perform exactly as it did two or three years ago is unrealistic. Accepting that these changes form part of the condition isn’t the same as giving up. In fact, it’s exactly the opposite. By accepting the reality of the deterioration, I can take practical steps to adapt to it. Adaptation is the key to keeping independence and quality of life. If large supermarkets are too much to handle, I don’t stop shopping entirely; I change how I do it.

And here are my tips:


  1. Time your visits carefully: Avoid peak hours. Go to the shops early in the morning on a weekday, or late in the evening when the crowds are gone, the noise levels are lower, and the environment is calmer.

  2. Shop smaller and local: Reduce scale. Swap the massive superstores for smaller, local shops where the layout is predictable, the choices are fewer, and the staff are familiar.

  3. Use a highly detailed shopping list: Externalise memory. Organise the list by aisle or section beforehand, so there is no need to make decisions or search aimlessly while in the shop.

  4. Protect your energy levels: Manage fatigue. When speech starts to slip in the evenings, recognise it as a signal that the brain needs rest. Keep conversations simple, do not force the words, and give yourself permission to step back and rest.


My family and friends have adapted too. They‘ve learned to give me a little extra time to find my words, to fill in the blanks gently without making a fuss, and to understand that if I call something by the wrong name, it’s just the illness talking, not a lack of attention.


The Determination to Fight Decline.

I’m sharing these struggles not to court sympathy, but to give an honest account of what it means to live out this diagnosis day by day. It’s a life of continuous negotiation with a condition that’s always trying to take a little bit more. But while the disease might be changing the rules of the game, it hasn’t won.


Every single day, I get up with the determination to do all I can, to meet whatever new hurdle appears, and to fight the decline with every tool at my disposal. That fight doesn’t always look like a grand, dramatic battle. Most of the time, it looks like a steady persistence. It’s the decision to keep going out into the community, even if it's on a smaller scale.


It’s the choice to keep talking, even when the words come out wrong, and I have to laugh at myself for asking for an apple instead of an orange. It’s the effort to stay active, stay connected, and keep embracing joy in the present moment, regardless of how the landscape changes.


The deterioration is real, and it is a heavy burden to carry at times. But the human spirit is remarkably resilient. I’ll keep adapting, keep learning, and keep moving forward, doing my absolute best every step of the way.

 
 
 

1 Comment

Rated 0 out of 5 stars.
No ratings yet

Add a rating
Guest
2 days ago
Rated 5 out of 5 stars.

Good blog Peter but failed to mention the loud music and the tannoy and attending sporting events and the crowd

Like
bottom of page