Severe Alzheimer patient forgets how to push healthy soft stools out. Needs to be fingered out every 3-4 days. Tried all stuff to promote diarrhea - nothing. Not pleasant task. Guy is still healthy, likes to walk, eats well - lots veggies/fruit.
Any other suggestions to cope?
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This reminded me of something that happened between my mom (co-caregiver w/ me) and my dad (Alz pt). My dad was a big guy, getting more stubborn and violent about it as the weeks when on. I was pressing my mom that it was dangerous to continue trying to keep him home but she was resistant.
One day she called me over, afraid because he had pushed her and she had locked herself in her bedroom that we had readied for just an occurrence. She had been helping him with some bathroom clean up, something he didn't like, when he snapped and came at her like a gargoyle, teeth snarling and arms out reached with fingers like claws grabbing towards her. He shoved her backwards hard enough that she came out of her shoes. Had she landed one foot to the left, she would have rolled to the floor and very possibly struck her head on a piece of furniture with devastating results. Luckily she went to foot to the right and landed with her backside laying on the bed. Dad was still coming at her to attack, she raised her legs and kicked him backward. He stumbled and crumpled gently to the ground as she ran out of the room, turning the bathroom style lock on the door handle and closing him in his room.
I arrived in less than 15 minutes, she was in her protected bedroom space and he hadn't come out of his room, not remembering how to open the lock which was on the inside of his door. My mom let me in her bedroom and told me the story. I told her it was very dangerous and asked her if she was ready yet to place in a home. I know she was scared this time but as she was thinking it over he managed to calm down enough to open his door and come out in the hallway. Sadly, when he couldn't find anyone there, as we were both quietly still in her bedroom, he started calling out in the most pitiful manner, scared to be alone and apologizing for being bad. My mom said no, see, he didn't know what he was doing, he didn't mean it , I can't do that to him.
Not two days later she called me up and said to find a place because she couldn't keeping it home anymore. I already had some contacts because I had my aunt in a nursing home so I made some calls. It took about 3 hours but I with able to find a place, they faxed the doctor who faxed back a diagnosis of "organic affective disease" and it was all set for him to be admitted the following day.
I went over to tell my mom and aster something else carry had happened that made her change your mind. She said yes indeed had. I said tell me. She said well, he was sitting on the bed and I was trying to help him put on his shoes when he grabbed the one I was working with out of my hand and bent over to put it on himself. as I stood there, all of a sudden I got a feeling that I wanted to beat him on the head. I didn't but I wanted to. And I knew if I didn't do what you've been suggesting and put in with somebody can take care of him, there might come a time that I break down and do that.
Wasn't that amazing? He pushed her across the room with such force, she could have been really hurt. But SHE was afraid she was going to hurt HIM ! !
every 3-4 days he has stains in diapers indicating he needs to poop.
If brain is now unable to send message to him to push poop out, nothing we can do! Found a product of small plastic ball containing salt solution and glycerin for enema. Used it on him standing up but not too effective. But it helped to lubricate passageway and 'fingering' poop out was smoother. Really need to do the enema lying down, but patient not likely to co-operate.
The patient is my spouse of 54yrs, now aged 80 with Alzheimer's since 2002. He is physically fit - eats and sleeps. Loss of language and comprehension makes him a walking vegetable now. He is mostly quite cheerful.
I am lucky, I can afford to send him to day care centers for Alz.. Without this respite I would have drowned long ago - or drowned him! I am lucky I am fit and strong still to push and pull him - I do have a home helper too. This end stage may go on for a long time!
THERE SHOULD BE SUCH FACILITIES TO GIVE CAREGIVERS RESPITE EVERYWHERE AND AFFORDABLE!
I am hanging in there and waiting for the end to come.
I appreciate all the hugs I can get!
Love to all in the same boat
Gwendo
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Lying down for an enema is the ideal position but if you insert the catheter as high as possible before he sits down you can do it on the toilet. You need a regular large guage catheter which can be reused if necessary many times and as much as several pints of warm soapy water. It won't harm the rectum as it runs right out into the toilet like a lavage
One good thing about end stage is the patient sleeps a lot during the day. The brain is diminished and gets quickly tired with any kind of activity ranging from a shower to eating a meal. This gives needed respite for me as at week ends, I am coping on my own.
Pills have to be ground up and mixed with food as this patient spat out large capsules/pills a year ago. He does not seem to mind powders on a spoonful of any food. I also need to give liquid forms of Omega fish oil.
Thanks for all the tips. This is a wonderful blog to get needed helpful info.
Gwendo
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Caregivers of AD need to be smart.,Doctors not much help. If you tell them they are getting rigid - is it Parkinson's - they will say maybe but offer no other help. I need to go on-line, look up symptoms, find if there is medication and then go see the doc and tactfully ask if SINEMET might work! So no help with the bowel problem either, except to treat as constipation!
thanks, Ferris1, for suggesting magnesium. given once so far - 175mg and going into 2nd day. Interesting! In middle of last night for a diaper change. he is sitting on toilet, did a pee and unwilling to get up. Asked if he has poop. He says yes! I did not believe and got him up and yes he has poop indications when wiping his bottom. But he still does not push and we need to finger it out. but it is a step forward that he knows he needs to poop. And this is less than the 3-4 days since last 'fingering'.
So with more magnesium and Sinemet, we may have more reaction. I will keep you all posted!
Thanks for all the hugs and encouragement. We all sure need it with this terrible disease.
Gwendo
It is a spouse, married for 54 yrs and knowing all his funny habits, its hard to put him in a home as we are coping still. I am very fortunate I am very fit n healthy with physical strength to push and pull him. though this is getting harder.
Before he became completely incontinent, nights were very disturbed. Pooping was no problem either. Now I sleep all night! How to do it?
I got a hospital type bed, so he is 'trapped'! Now easier to pull him up too.
I change from pull up to wrap round diaper at around 11pm and also hope to get him to pee in the toilet first. I try to make sure the diaper is higher at the back than at the front - not easy as spouse is not helpful and his hands hang on the diaper as he stands.I need to take it slowly!/. When all done we can all sleep the night until morning. Sometimes the towel and plastic sheet under him, as well as his pants are wet by morning, sometimes if diaper done well - all is clean!
Another tip is to give him shorts to wear at nights that has tabs for a belt and to belt the shorts tightly. Men like to put their hands into their pants and 'fiddle' - pee comes out all over the stomach and the bed! Now that problem is solved!
Showers just take a bit of time to persuade him to go into the shower. Once in we get it done very quickly, sometimes some resistance.AD patients cannot see water and it frightens them.
I do manage to have a life as I send him out to day care daily. I am lucky to be able to afford this, as well as a live in helper since last year. It costs me less than residential care.
so my one problem is the poop! I will try giving him magnesium as one of you suggested. I take them myself as I get night cramps when I walk too much.
It is these last three years as we go into end stage that has been hard. After what was a long and happy partnership, it is the least I can do for him - even though it has become more of a hate relationship now.
The end must be near soon!
Gwendo
PS...GREAT advice from all of you for my future reference!
Ativan keeps him calm. I used to give him a dose daily, but he also just got sleepier and sleepier. It works within 1/2 hour and he is very happy and co-operative and then passes out almost! I managed to get away for 10 days to see my son. On my return he was so happy to see me, that I stopped the Ativan. he has been off it for over many weeks now. Beginning to get more grouchy and so I give it sometimes. I think it builds up in the body too much.
Come to think about it, the bowel problems began around when I went off in March. My absence triggered it? The report I heard was he was quite happy and manageable in my absence. I found a wonderful live-in helper last year and she saves my sanity. gwendo
the guy is 80 yrs old and AD since 2002. so we are getting to the end, but it may be a long time coming as he is so fit. still walks, eats and sleeps well. mostly cheerful but can get easily tired when he will get violent a bit. does not really hit me - just threatens to do so! I follow the advice, leave him alone for a while to stew.Then I manage to get him in bed, he falls asleep immediately and wakes up angelic!
Was incontinent since last summer. Now, if timing is right, can pee in toilet but the poop is stuck. I can tell because a wipe is dirty. He has not wiped his own bottom for years! Pull up diapers are wonderful, hi-tech material means it can hold several pees too without getting sore cos of one way pass through layer.
He is not constipated. As there is indication of poop from a wipe - and even if I sit him on toilet for hours with a magazine to flip , he does not push out! the indication is there every 3-4 days. When we do a finger job, there are huge amts to pull out. He does not help much, but standing he does sort of bend a bit, which makes it easier to finger out. S o not constipated and this is why I am trying to give him diarrhea!
He eats oats daily, Plenty of green vegetables and fruit. Prunes and prune juice, fresh oranges, yoghurt, blueberries. You name it, he eats it. He has a very very balanced diet.
I could give him a soapy enema every now and then instead of the fingering. it will be real messy and not sure if he will submit to this as it is better done lying down. His comprehension is very slow , if at all, so he mostly does not co-operate.
coping with him for11 long years and I have had it. I wish he would die soon. Yes it is depressing, but I cope and have to get on with it. When he no longer recognizes me and is bed bound - I will get him into a home. By then it should be the end.
I do not think there is any suggestion I have not tried. there is no blockage - he just does not push any more.
Gwendo
Good Luck