← Return to No Longer a Caretaker. What am I?

Discussion

No Longer a Caretaker. What am I?

Caregivers: Dementia | Last Active: 2 days ago | Replies (31)

Comment receiving replies
@celia16

I haven’t placed a spouse for care, but I did place a relative. I was responsible for my cousin’s care, after she got dementia. After seeing it was not possible for me to care for her in her home, I found an excellent Memory Care facility. Caregiving does not end after placement. There are many responsibilities that continue. She relied on me a lot and my visits were vital. I will say that much of the strain of daily hand’s on care is relieved.

I was fortunate in that I never felt guilt over the placement, only pride that I had done the right thing. Caring for someone 24/7 solo who has substantial need just isn’t feasible. It’s not fair to either person. I realized what she really needed and arranged it.

I hope you will feel better as you get a chance to adjust Some people with dementia settle in and seem comfortable, but others might not. I observed many residents with dementia over the six years I cared for my cousin. I found that sometimes with dementia a person might not be able be content or happy no matter where they are. Meds can help, but it’s not always apparent. I learned to temper my expectations.

After a couple of weeks, my cousin thought she was living in her new apartment and liked it a lot. She adored her new friends there, though they didn’t really talk to each other.

Jump to this post


Replies to "I haven’t placed a spouse for care, but I did place a relative. I was responsible..."

I have hope that my husband will reach out to the other men in the Memory Care Area. He was never social; a doer, a worker who much preferred to build a structure or renovate a house than socialize. I have to curb my expectations knowing his lifelong proclivities for hard work. I think women, being more social in general, have an easier time to acclimate to new people and new surroundings. I have always been his social outlet and will continue to do so. Without the added stress and burden of physical care, I feel I am ready to go back to being Miss Sunshine. Watching people in a Memory Care Unit is like watching toddlers in parallel play. They enjoy knowing others are there, but don't feel compelled to interact with them. It is important not to project what you think they would enjoy and want to do as seen through your own eyes. This is a whole new chapter. Obama had a great line in a book, "This..sh..t would be interesting if I weren't in the middle of it." That is exactly how I feel.