Table of Contents:

  1. Quote of the day

  2. Extra Protection When You Can’t Always Be There

  3. Interesting stories this week

  4. Dementia Myths Debunked: 3 Common Misconceptions That Delay Diagnosis

  5. Responding to YOU!

  6. A quick note (for those still working while caregiving):

My caregiver mentra is to remember: The only control you have is over the changes you choose to make.

Nancy L Kriseman

When seconds matter, help should be simple

A conversation that comes up in many families is a simple one:

“What would you do if you needed help and couldn’t reach the phone?”

It’s not always an easy conversation, but it’s one that tends to come up as independence
changes.

One option some families explore is a medical alert system that allows the person to call for help from anywhere in the home.

You can see how it works by clicking the link below, or speak directly with their team on 1-877-327-0779

Only available in the USA

Interesting Stories This Week

Cholesterol drugs may reduce dementia risk

UK dementia diagnosis support programme

Men’s brains shrink faster than women’s

Unusual clothing choices as dementia sign

New treatments show promise for memory

Dementia Myths Debunked: 3 Common Misconceptions That Delay Diagnosis

When someone forgets where they’ve put their keys or struggles to recall a name, it’s easy to brush it off as “just getting older.”

But sometimes, it’s not.

One of the biggest challenges with dementia isn’t just the condition itself — it’s the misunderstandings that surround it.

These myths can delay people from seeking help, sometimes for years. And that delay matters more than most people realise.

Research suggests that the gap between first symptoms and a formal dementia diagnosis is often over three years. That’s three years without clarity, support, or access to the right care.

In this article, we’re breaking down some of the most common myths — and why letting go of them could make a real difference.

Why Dementia Myths Are So Harmful

Myths don’t just create confusion — they create hesitation.

They make people second-guess what they’re noticing.
They delay conversations with doctors.
They push support further out of reach.

And the reality is, earlier diagnosis can open doors:

  • Access to treatment and support

  • Time to plan ahead

  • More opportunities to maintain independence

  • Better understanding for families

Let’s look at the myths that often stand in the way.

Myth 1: “Dementia is just a normal part of ageing”

This is one of the most common — and most damaging — beliefs.

Yes, some memory changes can happen as we get older. But dementia is different.

What’s the difference?

  • Normal ageing: occasionally forgetting names or misplacing items, but remembering later

  • Dementia: memory loss and confusion that interfere with daily life

For example:

  • Struggling to follow conversations

  • Getting lost in familiar places

  • Repeating the same questions frequently

  • Difficulty completing everyday tasks

Why this myth is harmful:
When people assume it’s “just ageing,” they delay seeking help — often until symptoms become more severe.

Myth 2: “Only very old people get dementia”

While dementia is more common in older adults, it doesn’t only affect people in their 70s, 80s, or beyond.

The reality

Younger-onset dementia can affect people in their:

  • 40s

  • 50s

  • 60s

In these cases, symptoms are often overlooked or misdiagnosed.

Changes in behaviour, mood, or performance at work might be attributed to stress, burnout, or mental health — rather than something neurological.

Why this myth is harmful:

  • People don’t seek help early

  • Families may not recognise the signs

  • Diagnosis is delayed, affecting careers, relationships, and future planning

Myth 3: “Dementia means Alzheimer’s”

Alzheimer’s is the most well-known form of dementia — but it’s not the only one.

Dementia is an umbrella term

It includes several different conditions, such as:

  • Alzheimer’s disease

  • Vascular dementia

  • Lewy body dementia

  • Frontotemporal dementia

Each type has different causes, symptoms, and progression patterns.

Why this matters

When dementia is misunderstood as a single condition:

  • The wrong assumptions may be made about symptoms

  • Support may not be tailored correctly

  • Families may struggle to understand what’s happening

Getting the right diagnosis helps guide the right support and care.

What Caregivers Should Watch For

If you’re supporting someone and something doesn’t feel quite right, trust that instinct.

Look out for:

  • Increasing confusion or disorientation

  • Changes in personality or behaviour

  • Difficulty with everyday tasks

  • Withdrawal from social situations

  • Repetition or memory gaps

You don’t need to have all the answers — just noticing patterns is enough to start the conversation.

What to Do If You’re Concerned

If you’re worried about yourself or someone else:

1. Don’t wait

It’s always better to check early than to delay.

2. Speak to a GP

They can begin the assessment process or refer you to a specialist.

3. Keep a record

Note changes in behaviour, memory, and daily functioning — this helps during appointments.

4. Involve family where possible

Having support makes the process easier to manage.

Watch and learn more

If this story resonates with you, you are not alone.

We share regular insights on our YouTube channel, covering topics such as caregiver guilt, emotional overwhelm, and the realities of caring for a loved one with dementia.

These videos are designed to support you with honest guidance and reassurance when you need it most.

A Problem Shared is a Problem Halved

Every week, we share an honest story from a caregiver — the things most people are too afraid to say out loud.

This Week’s Caregiver Story-

“I’ve started to feel unsure about social media and what’s right or wrong.

Sometimes I post about our life, small updates or moments, and people are really supportive. But then I wonder if I’m sharing too much, or if I’m taking away his privacy without meaning to.

At the same time, social media has been one of the only places I feel understood. I see other carers going through the same thing, and it makes me feel less alone.

I just don’t know where the line is between sharing for support and protecting his dignity.”

Harvey says:

Thank you for raising this. It is a thoughtful and important question, and one that many caregivers are beginning to face more often.

Social media can be both a source of support and a space that requires careful judgement. On one hand, it allows carers to connect, share experiences, and feel less isolated. On the other, it introduces questions around privacy, consent, and dignity, particularly when the person you care for may no longer be able to fully express their preferences.

The fact that you are asking this question suggests you are already approaching it with care and respect.

There is rarely a single clear boundary, but some carers find it helpful to reflect on a few guiding principles. For example, whether the content honours the person’s dignity, whether it focuses on your experience rather than exposing theirs, and whether it is something you would feel comfortable sharing if they were able to fully understand it.

It can also be helpful to distinguish between sharing for connection and sharing for exposure. Supportive communities can offer real value, especially in a role that can feel isolating.

At the same time, it is okay to set personal limits around what you choose to share. Protecting both your wellbeing and their dignity can exist together.

You are navigating something that does not have a simple rulebook. Thoughtfulness, like the kind you are showing, is often the best guide.

And you are not alone in trying to find that balance.

Harvey

Want to share your story?

If something’s been on your heart lately, let us know. We read every word. Your voice could offer comfort to someone else navigating the same journey.

A quick note (for those still working while caregiving):

Over the past year, I’ve been speaking more with companies about something that keeps coming up — how many employees are quietly balancing work with caring for a parent or loved one.

In many cases, its affecting stress, focus, and even whether people stay in their roles.

I’ve recently started working with a small number of organisations to support these employees in a simple, structured way — without adding pressure to HR teams.

If you work at a company where this might be relevant (or know someone in HR/People teams), feel free to reply and I can share more.

At All About Alzheimer's we're dementia professionals but we're not medical doctors or lawyers. The information we provide is for general informational purposes only and should not be considered as medical or legal advice. Always consult with a qualified healthcare professional for medical diagnoses, treatment or any health related concerns and consult with a lawyer on any legal issue.

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