Three weeks into AL and my aunt was improving slowly. She started PT and seemed to be getting stronger. She got a bladder infection last week and has been on antibiotics. She’s refused to eat or take her meds in the last 24 hours. I spent the entire day with her. She has at least 3 nurses hopping all day and all night. It’s never enough. She’s become incoherent and says things that make no sense. She grabbed my hand and began pushing it then wanted to know why the channel on the TV wasn’t changing. She’s shakey and confused more than I’ve even seen. The simplest of tasks are no longer staying with her. She screams out in the middle of the night and scares the other residents. She seems to be fading fast. Has anyone experienced this?
If your aunt has a bladder infection, that can lead to lots of confusion....I've seen it with both of my parents. Almost delirious behavior at times until the antibiotics clear up the infection. That's what you may be seeing with your aunt as she fights the bladder infection off. If she has other health issues combined with the bladder infection, its possible her body isn't capable of fighting all the issues plaguing her, in a weakened state, and that's why she's fading fast.
Speak with her hospice nurse to get their take on what's going on as these nurses are very good at predicting their patients prognosis. If she's approaching the end of her life now, the nurse should be able to prepare you for that.
Best of luck with a difficult situation
Hospice is an end of life thing. Dr feels patient will be gone within 6 months. Not that people haven't lived longer. Some meds are stopped others like morphine introduced for pain and breathing.
You should not be using ur own money for ur Aunt. If she can't afford the AL then u sign her up for Medicaid. Then allow the State to take over her care. Tell ur cousin if he/she does not like it, then she can care for ur Aunt.
my dad was switched to hospice after having had COVID. My guess is your aunt was no longer showing improvement from her PT. Hospice does not pay for PT services - only comfort care related medical needs, in some hospice programs they will provide massage. Dad suffered from dementia and was at times angry, irrational, depressed and unhappy. It made him a difficult patient. He was with hospice for about 1 1/2 years.
on another note, you mentioned feeling financially and emotionally burdened by this job, and that it was affecting your family. I can relate. I was the primary caregiver for my dad (everyone else was over an hour or more away, or out of state). My brother was POA, I was MPOA. I was very uncomfortable doing so, but I did request payment several times when dad was staying at my home prior to finding a good assisted living residence.
It’s difficult enough to care for immediate family, and if you are not being compensated for your time, as kind as it is for you to give back to your aunt in this way, you may want to sit down with your family(husband and children) and decide what you/they think your role should be. Then write a formal letter or email to your aunt’s immediate family members with your decision spelled out - and any requests for monetary compensation for what you’ve done or are willing to do.
Expect a volatile reaction from your pushy cousin, but don’t back down. Bullies can’t bully when you don’t let them. You may have to cut off interaction with that extended family entirely - including your aunt, but remember YOUR own family comes first, as does your own health. Just keep restating your terms as you wrote them. If they refuse, then leave the situation. It will be hard, but you need to show them you’re not a pushover.
It’s possible your aunt is close to the end, and you won’t need to do this. Either way - sending hugs. It’s NEVER easy to be a caregiver for someone who can be challenging to work with, it’s difficult enough when they are sweet!