Hi, all,
First, a belated thanks to this board for all the support the past 2 years. Dad is in Assisted Living now (went in last November) and Medicaid was approved two weeks ago. Yay. This board was a huge support to me even if I did not post often. So thank you.
My question now is this: The facility has allowed my father to manage his own medications but recently he is getting more confused and not storing/taking his meds correctly. The nursing director gave me the heads-up that he is going to switch the meds to being administered by the facility. I am fine with this. But dad is going to flip out over it. How do I convince him that it's the right thing to do? The last time the facility was going to do this they gave him one more try. Obviously it didn't work. At that time my father was livid that they were taking away this part of his control and would rant to me all day for a week. Any advice?
When he begins to rant, say "Dad, this isn't in my control or yours. We can talk about something else or I'll have to go".
Don't entertain the ranting.
one.
This was one of several tips I learned from the smarty folks here. It came late in my caregivers journey - unfortunately I found this site in year five of six - but nonetheless...
The act of politely saying “... I’m gonna go now. I’ll come back on day when you’re more up to a visit” works wonders iIn a variety of situations when the elderly loved one is attempting to take their anger and frustration out on you.
Tell Dad that the ALs policy has changed by State law. Residents are no longer able to have medications in their rooms. Violation of this policy could mean penalties for the AL and his rent going up. 😊
Then if he rants let him. Nothing u or he can do. You can always walk away.
Let him be angry and rant for a time, I have loved ones that I have a time limit set for this behavior, after that time is up, on to another subject or I am gone. As humans we need a safe place to vent, but we don't need to be allowed to obsess about what it is that we are venting about. So give him a safe ear and move on after a set time or whatever you are willing to do.
Best of luck, this is a battle for sure.
Assisted living did not like his laxative addiction. He'd want me to sneak out and buy him some. I'd compromise and buy them from Amazon and have them shipped to him. They would help him open the box and they would confiscate them. This way I was not the bad guy.
When I noticed mom wasn't bathing herself regularly, I asked the facility to come in and help her in the mornings and mom resisted in the beginning. I finally told her that the hand held shower sprayer was really difficult to use and everyone was complaining so they have to have someone come in and help everybody in the morning to make sure they can manage the sprayer and not slip and fall while doing it. She seemed to go along with that...
It's hard to get into the mode of "fabricating" stories to our parents, but if it's in their best interest...I feel justified.
Good Luck
When mom was still living in her condo, but having difficulty remembering to take (or maybe even over-taking) her meds, we were in process of starting to bring in aides. The nurse sent to evaluate her confirmed what I knew - early dementia. Her recommendations included getting a timed locked dispenser. For only 1x/day, it would be probably a month's worth. It can have other times set, so some morning, some evening, then it would be 2 weeks before refill.
The aides hired would not be able to dispense the meds, but they could check the dispenser and remind her that she hadn't taken them yet (she would not hear the alarm or miss the blinking light.)
The staff can keep his meds and set up the dispenser, checking on him to be sure he takes them. This way he would still have some "control".
Whoever does, though, there are - as you have already identified - several steps to Medicines Administration. What the ALF ought to be doing is involving your father in as many of them as is practicable, in line with the end result that: the Right Person gets the Right Medication in the Right Dose in the Right Manner at the Right Time.
So, counting them off...
Ordering repeat px's.
Collecting same.
Storing.
Dispensing.
Following directions.
Taking.
Recording.
What cannot be done BY your father must be done in front of him, and explained to him as it is done, each and every time. Your father's right to refuse a particular medication, and his right to know what he is being offered and what it's for, must be respected.
The explanation must be comprehensible to the person expected to understand it. So for example: with some clients, you'll say "this is the Apixaban" and they know much better than you do what it is and what it's for; with others, you might tell them "this is the medicine to stop dangerous blood clots in your circulation."
The facility ought to have some sort of Consent to Medications Administration form which explains how the process works, and which somebody ought to be asked to sign. This would also be an opportunity to reassure your father that his material rights - to be treated only with his informed consent - will remain intact.
There are two extremely sound reasons for people to be uneasy/resentful/livid about their medications being taken away and then handed to them by staff. One, they may not have that much confidence in the staff. You say your father's not storing/taking his meds correctly? I'll bet he'll come right back at you with "what makes you think THEY will?" Two, they may not be happy that they know what they're being offered.
They are *right* to have these concerns, and the facility must reassure them by explaining their safe handling and administration protocols.
I think that our point is, Dad's argument should not be with his daughter; this is not something that SHE is taking away from Dad; it's the facility that is doing is (with her agreement). Dad's fight/rant, if he wants to have one, is with the facility, not with his daughter.
There is always a fine line, isn't there, where a client's "independence" is concerned? We want them to be independent, but we'd much rather that they not end up dead because of that independence.
If dad refuses the Medication Management services, he is free to move elsewhere. And his daughter is well within her rights not to help him do so.
Having read more, including Nanulinda1's post about her sister breaking into the drawer... perhaps the dispenser isn't such a good idea. It would be very easy for him to break.
So, alternative, make up a document with a table listing all the meds and when/how much to take for him. The heading should have his name and the top line of the table should have the information for each medication at the top of the column and the first column heading is the date/time, to be filled in by him with a check mark under each medication taken that day.
If he has this, he can check off each medication as it is provided, giving him *some* control, in a sense. More like busy work, but if he's going down the dementia path, it might work... Of course he could end up just writing whatever and checking everything... Dementia is just SO much fun...
Blaming the facility, his doctor(s) or even the government would possibly take the heat off OP... It's really a discussion that should be diverted to something else, whenever possible as you will NEVER get him to agree... just go along with him, commiserate and point fingers at who/whatever you can as to being the source of this change! Promise you will meet with whoever and get to the bottom of it. One useful upside to dementia is that they will forget, so you can promise every time... Preferably it would be an entity outside the facility, then his railing to you or staff can be challenged by telling him it is the doc or gov't directing this. Have him write letters to his doc and/or rep (never to be sent) to complain to the doc or gov't! More busy work!
Or, I am sorry, dad, I did not know this was going on... I will try to talk to the director, but in the meantime, please cooperate..
New manager - new policy --- (That is good.)
Love You Dad. GoodNight
my neighbor asked where he could dispose of his parent's meds. Parent died, and he found a couple of huge zip lock bags of meds... no idea what they are. He is afraid to take them to the police station. There is a bin for drugs--legal, illegal, just dispose of them there. I told him I would drop them off.. He is concerned about video?/// why.....Someone said put them in a can of coffee beans... like that is going to absorb them?... possibly... but then what, take the coffee beans to the police station and make them dream of donuts all day? I just don't know. donut holes? :)
Not sure how many he takes a day, but they have 'pill packs' that can be ordered with all of his meds put into sealed wrappers to take at certain times, am, lunch, pm. They are dated so if he forgets if he took or not, the date on next pack would remind him. They also have dispensing machines that sound an alarm when it's time to take and all of the meds for that time period are dumped into a cup at one time. He could keep those in his room and it would ensure he had a pack of pills to take at the designated time without having to open multiple bottles to get his meds. This is really all about taking one more thing away from him and his independence. If there is any way to maintain his usual daily tasks, it's worth a try.