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Welcome to the Caregiver Forum!
This is the place to connect with others who are on the same caregiver journey as you. Here, you can share your experiences, find support, or just chat with others who truly understand the hardship and, yes, even the occasional joy of being a caregiver.
This community is here to provide you with the emotional support and practical advice you need. Feel free to ask questions, share your stories, and offer advice based on your own experiences.
Remember, you are not alone on this journey. Our f...
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Showing 21 - 30 of 51 active discussions
2
Feeling Overwhelmed - Need Support
I've been caring for my mom for 3 years now and lately I'm feeling completely exhausted. Between work, caregiving, and trying to maintain my own life, I feel like I'm drowning. How do you all manage the emotional toll? I know I need to take care of myself but I feel guilty whenever I take a break.
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Dealing with Sundowning Syndrome
My father experiences increased confusion and agitation in the evenings. His doctor called it sundowning. We've tried keeping lights on and maintaining a calm environment. Has anyone found other effective strategies? It's really challenging for our family.
2
Tips for Managing Daily Routines
I wanted to share some strategies that have helped me maintain a consistent daily routine for my mother who has dementia. Creating a structured schedule has really reduced her anxiety. What routines have worked for you?
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🦃 Happy Thanksgiving from Pat’s Gameplan
As Thanksgiving approaches, we want to take a moment to honor you — the caregivers who give so much of yourselves every single day.
This season can feel different when you’re caring for a loved one. Traditions may change. Guest lists may be smaller. Schedules may look nothing like they used to. And that’s okay.
We’d love to hear from you.
💬 Tell us in the comments:
What will be different about your Thanksgiving this year?
Are you starting any new traditions?
What is one thing...
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5
When is it time?
Love the website, lots of great content. The Share My Story videos are my very favorite. I am caring for my FIL, who honestly fades in and out of reality at this point. What are the markers, or indicators that a facility with memory care is needed?
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It's been harder than I thought it would be!
Hello everyone, my name is Barbara and I’m grateful to be here. I live in southern Louisiana with my husband and our three kids, and for the past three years I’ve also been a full-time caregiver to my father-in-law, Larry. He was diagnosed with early onset Alzheimer’s at 67 and now, at 71, we’re starting to see deeper cognitive decline. This forum feels like a lifeline — a space where people like me, who are doing the best they can with very little guidance, can finally ask questions without fea...
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Anyone else's emotions all over the map?
Lately, I’ve found myself struggling with a wave of emotions I didn’t expect—especially anger. I’m not proud of it, but I’ve been snapping at my husband over the little things. He asks me the same question again and again, and instead of calmly repeating the answer, I lose my patience. When he was first diagnosed with Alzheimer’s, I was able to stay calm, grounded, and full of compassion. I thought I had a handle on it. But now... now I feel like I’m the one falling apart.
It’s confusing beca...
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5
Caring for FIL who refuses to shower
Just as the title states. I am the main caregiver for my father in law and in the past 5 days he has fully refused to shower. He keeps telling me that he doesn't need to shower because he "just took one", there isn't any amount of reasoning I can do to convince him otherwise. This is a new problem, but I can only see it leading to his placement in a memory care facility. Has anyone experienced this?
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Treatment Options?
I am currently caring form my father who was diagnosed with early onset dementia. I am reading about several treatment options that others have pursued. Specifically we are interested in any experience anyone has had with Kisunla. We would also be interested in another treatments that anyone has experienced and their experiences whether positive or negative.
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Is a dog a good idea?
I'm caring for my FIL and we are struggling to get to daily exercise every day. I was thinking if we could get a dog that would give us a reason to exercise daily. Is this a good idea? Overall what are the expectations of someone with dementia? Does the dog work well or would this be something that he may come to resent? Looking forward to hearing your experiences.
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