It's not that I don't have help - I do. It's just that every time I have someone else take over for an hour or two, there seem to be 6-8 hours worth of activities that I need to squeeze into that hour or two. Like sleeping, food shopping, errands, walking the dog, social activities, exercise and other recreation.
My brother and his wife flew into town today to spend a little time with my mother while they still can. They would like to take the local siblings out to dinner tonight. No, I can't leave Mom, and I'm too exhausted at this point to go out anywhere, even with my brother who's in town for one day. My dog is getting very short walks and I'm picking up only the bare essentials at the closest supermarket and rushing home to relieve whoever is sitting with Mom while I go out.
I told my sister on the phone today that if this goes on much longer, I will need more help, especially at night because I'm getting up with Mom so often in the night that my sleep is totally fractured. She offered to stay over three nights from now and take care of Mom so I can sleep through the night. And hopefully watch the late news with the sound on, which I haven't been able to do in many days since I can't have the tv drowning out Mom's call.
I'm sure many of you have been through this and have lots of thoughts or advice so please don't hesitate to share. I'm all ears!
When my husband and I first decided to start dating, one of the first things he felt was important to set straight right from the start was....
"I'm not a mind reader., You must tell me what you, want, think and need."
Since then I keep that in mind when dealing with others as well. Saves me lots of inner frustrations and silent resentments.
My Mom is on hospice also. They have a volunteer program for respice. Does yours provide this service?
You and Mom are in my thoughts and prayers. Thank you for being here for us💖🌹
What are the chances of home health care coming out? I hear they’ll give you 30 hours a week. And, what about a facility? I know that for some families and their loved ones, “placement” is a dirty word. It’s just upsetting when I read someone I admire is having such a hard time. Sending hugs.
I think what I would do is take a few minutes whenever you think of something you need, and create a checklist, prioritized if appropriate. Indicate what only you can do, and what can be done by others.
When folks call to ask what they can do, tell them about the checklist, available if they want to stop by. Or you can e-mail it. Hopefully they'll choose something and follow through.
I created a shopping list for Dad, by category and the brand he preferred to give to folks who offered to shop. All they had to do was take the list, with items checked off, and get them.
What kind of errands need to be done, and who can do those? Neighbors? Friends?
Walking the dog: neighborhood kids? Local Scout troop? Or search for a local dog walker; my sister used to do this in her spare time, and got paid for it by her clients. Unless it's a break for you, someone else can do it.
Perhaps you can capitalize on the offers to volunteer and turn them into social activities. Exercise - perhaps a few minutes at a time. Recreation is harder unless you can treat visitors as recreation. Someone can watch Mom while you take a walk.
One thing I did when I knew Dad was near the end was to make the hard decision to let everything go until it was all over. Other than eating, laundry, dishes, an occasional vacuuming, and immediate financial issues, everything else was just postponed. But Dad was in a facility for rehab, stayed through palliative care and until the end. Still, I had his house and mine and needed to keep checking his for security issues.
I think the best decision I made though was to keep him at the facility and not try to bring him home, despite the fact that he had earlier repeatedly stated he wanted to die at home. There's just no way I could care for him 24/7.
I think that's the big decision that you'll face, i.e., who else can you bring in to help? I got a private duty firm in a few days; I wasn't pleased with 2 of the workers, but one was a gem. Still, I had trouble letting go and felt I needed to be there until things got settled (which didn't happen b/c he decompensated after release from the hospital).
What really helped me is to admit that I couldn't handle the situation, and that I would rely on help. That was a major issue for me. Kindly stated, I see that you're facing a similar dilemma. That's why it's important to accept that others can do for you what you're doing now.
As to the dinner arrangements, why doesn't one of the local siblings stay with Mom so you can go out to dinner? Even if you're tired, the break would be a tremendous relief. That's what I started doing after Dad went on PC. I stopped at a restaurant to destress, and it really helped.
I wish I could think of something insightful, but 24/7 care of a dying person at home, w/only hospice's limited involvement, is a challenge that is difficult to meet.
Edited to add: I see CW and I were posting at the same time, and along the same line.
People are willing to help, but aside from me, they're all trying to carry on their regular schedules while doing it. And they don't realize that an few hours here and there when it's convenient for them is just not enough to enable me to continue this over the longer term. Several people have said to me "Whatever you need, just ask". But I need them to call every day and say "What do you need today? Is there anything I can help with today?" Of course that's not what anyone says. I'm frustrated that nobody seems to understand this, but of course you don't understand unless you've been there yourself. Sigh...
Could you hire an aide to care for mom overnight so you can sleep? Maybe like the 7-7 or even 11-7 shift? It seems like that might really help if there is the means available to do that, even if it has to be just a few days a week.
Hugs to you. I hope you're able to get some relief.
See All Answers