Hey, Careblazers! If you’re here, chances are you’re a caregiver, or you know someone who is. First off, let me say this: all caregivers are incredible. Whether you’re caring for someone with a chronic illness, a physical disability, or anything else, there’s something truly special about the work you do. But as you know, if you’re caring for someone with dementia, you’re in a unique situation. We like to call you a Careblazer—a dementia care hero. 💪
Today, I want to talk about the big differences between dementia caregiving and non-dementia caregiving. Because while all caregiving is challenging, there’s something distinct about caring for someone with dementia. The emotional, physical, and time demands are on another level, and it’s important to recognize just how special and important the work you’re doing really is.
Time Commitment: Dementia Caregivers Put In More Hours
Let’s start with time. We all know that caregiving takes time, but did you know that dementia caregivers spend significantly more time than non-dementia caregivers? On average, a dementia caregiver spends 92 hours a month providing care, compared to 68 hours for a non-dementia caregiver. That’s a huge difference, and it shows just how much extra support someone with dementia needs.
And here’s another important point: 85% of dementia caregivers are unpaid family members. This means most of the caregiving falls on the shoulders of people like you—family members who are managing caregiving on top of everything else in life.
The Emotional and Mental Health Impact
Now let’s talk about the emotional toll. It’s no secret that caregiving can be emotionally draining, but dementia caregiving takes this to a whole new level. Research shows that 59% of dementia caregivers report high or very high levels of emotional stress. Compare that to 41% of non-dementia caregivers, and you can see the difference.
Dementia caregiving often comes with additional emotional challenges because of the nature of the disease. Seeing a loved one lose their memories, struggle with basic tasks, and sometimes not even recognize you can be heartbreaking. It’s no surprise that up to 40% of dementia caregivers experience symptoms of depression. So if you’re feeling overwhelmed or emotionally drained, know that you’re not alone.
Physical Health Takes a Hit, Too
Let’s be real—caregiving isn’t just emotionally exhausting; it’s physically demanding as well. This is especially true for dementia caregivers. Studies show that 35% of dementia caregivers report that their health has worsened due to caregiving. That’s compared to 19% of non-dementia caregivers. That’s a big difference!
What’s more, 40% of dementia caregivers report very high physical strain. This could be due to the hands-on nature of dementia care—helping with bathing, dressing, feeding, and even managing difficult behaviors. Over time, this physical strain can really take a toll on your body.
The Impact on Employment
Another major difference between dementia caregivers and non-dementia caregivers is the impact on employment. Many caregivers have to juggle work and caregiving, which is no easy feat. But here’s the tough truth: 57% of dementia caregivers have had to go into work late, leave early, or take time off to provide care for their loved one. For non-dementia caregivers, that number is lower at 47%.
This can create significant stress and strain—not just financially, but emotionally as well. Trying to balance a job while also providing intensive care for a loved one can feel like an impossible task. If you’ve been in this situation, know that you’re not alone, and it’s completely understandable if you’re feeling burnt out.
The Longer Journey of Dementia Caregiving
Here’s another key difference that sets dementia caregiving apart: the length of time you’re likely to be caregiving. On average, non-dementia caregiving lasts about four years. But dementia caregiving? That can last an average of 4.9 years. And as you probably know, dementia is a progressive disease, which means the caregiving demands only increase over time.
Unlike other types of caregiving, where a person’s needs may remain relatively stable or even improve, dementia caregiving gets more challenging as the disease progresses. It’s a long, tough road, and it requires so much strength and patience from the caregiver.
The Behavioral Challenges of Dementia
Now, let’s dive into one of the most challenging aspects of dementia caregiving: behavioral changes. As the disease progresses, people with dementia often experience behaviors that make caregiving even more difficult. They may become agitated, aggressive, or confused. But perhaps one of the biggest challenges is the fact that many people with dementia don’t even realize they have the condition.
Imagine trying to care for someone who doesn’t think they need help. It can feel like an uphill battle when your loved one refuses care, doesn’t recognize you, or gets angry when you try to assist them. This is a unique challenge that many non-dementia caregivers don’t have to deal with.
How Dementia Caregiving Differs: A Recap
So, let’s sum it up. While all caregiving is tough, dementia caregiving comes with its own set of challenges, including:
More time spent caregiving: 92 hours a month vs. 68 hours for non-dementia caregivers.
Higher emotional stress: 59% of dementia caregivers report high levels of emotional stress compared to 41% of non-dementia caregivers.
Greater risk for depression: Up to 40% of dementia caregivers experience depressive symptoms.
Increased physical strain: 40% of dementia caregivers report very high physical strain, compared to 19% of non-dementia caregivers.
Employment challenges: 57% of dementia caregivers have had to take time off work or adjust their schedules, compared to 47% of non-dementia caregivers.
Longer caregiving duration: Dementia caregiving lasts an average of 4.9 years, compared to 4 years for non-dementia caregiving.
Behavioral challenges: People with dementia may not recognize they need care, making caregiving more difficult.
What Would You Add to the List?
Now, here’s where I’d love to hear from you. What other differences have you noticed between dementia caregiving and non-dementia caregiving? Whether it’s the emotional impact, physical demands, or the long-term trajectory, there’s no doubt that dementia caregiving is its own unique challenge.
Personally, I think one of the biggest differences is the behavioral component. People with dementia often don’t realize they have the condition, which makes it much harder for caregivers to provide the help they need. What do you think? Let’s continue the conversation in the comments.
Final Thoughts: You’re Doing Incredible Work
To all my Careblazers out there, thank you for everything you do. I know the journey can be tough, and there are days when it feels like too much. But I want to remind you that the work you’re doing is incredible. You’re caring for someone who desperately needs your support, even if they don’t always realize it. You’re making a difference in their life, and that’s something truly special.
Take care of yourself, Careblazer. You deserve it. 💙
Want to watch the in-depth video that inspired this post?
Click the video below to watch. ↓
Transform Your Caregiving Journey: Join Our Care Collective Today 💖
Are you seeking deeper, more personalized support in your caregiving journey? Discover our Care Collective program, designed exclusively for caregivers like you. By joining, you’ll gain access to weekly support groups, engage in expert-led Q&A sessions, and connect with a vibrant community of caregivers who truly understand the challenges you face. Don’t navigate this path alone—CLICK HERE to learn more and become part of a supportive network dedicated to empowering caregivers with knowledge, compassion, and resources. Join us today and transform your caregiving journey!


One Response
Why don’t they drink enough?