Hi Susan,
I'm sure you're tried every approach possible. Sometimes, an "outsider" can do intimate things of this nature. For some reason the person isn't as humiliated as they are when a spouse or adult child helps. My mother-in-law didn't want family members to help with her showers, so we hired an in-home agency. This worked for awhile until she needed nursing home care. Obviously, toileting is going on every day. It seems to me that you may have gotten to the point where your husband would do better with nursing home care. Then you can go back to being a loving wife, spend quality time with him, but not be "the enemy" who forces him to use the bathroom, etc. Only you can decide, but there comes a time with most people where they can no longer provide all of the care for a loved one with AD.
Please let us know how you are doing. We're thinking of you,
Carol
Hi Susan
I am sorry to hear you are having problems caregiving to your husband. It is very common but is very stressful. Here are some links to shareposts that may help you.
Problem Behaviors in Mid to Late Stage Alzheimer's
5 Causes of Difficult to Manage Behavior in People with Alzheimer's
ABC of managing challenging behavior of Alzheimer's
I hope these are helpful. Remember that your husband does not do these things on purpose. It is the awful brain damage caused by this disease.
All my best wishes
Thanks, Christine.....knowing that my husband 'is not like he used to be and is not this way on purpose' has always assisted me in caring for him. At times, I would even go back and reread the portions of certain books that would give me more insight on 'meeting him where he was' with the illness. I read all of the websites that you listed and I appreciate the information. The cussing is not such a problem, but the refusal for assistance IS the problem. I need advice before this situation escalates and someone gets hurt (while trying to assist my husband). Thank you so much for any further information you can share with me so I can pass it on to the companions and staff.
Susan, it is always hard to help the person with ALlzheimer's or dementia in the area of toileting or taking a shower. My father-in-law has severe stage of AD and he does have trouble taking a shower so the nursing home only gives him one shower a week. They give him sponge bath in the face and private part in the mornings. My FIL wears a pull-up underwear/diaper. So now he sits down during the toileting business. He was alert with wet diapers before now he is a little bit oblivious with it. He still could strike out when they help him for toileting. So he is now taking low dose of antipsychotic drug provided that he is in severe stage (stage 7) and cannot walk/talk anymore. He hates water too. Also you need to test the water temp. first and prepare to tell him the steps patiently. If you do it as regular people's way, he won't like it.
Check with the doctor. If he is in stage 6/7, he may need some med. to calm him down.
Regards,
NC
NC, thanks.....my husband is on that type medication and they monitor it closely.
The staff has suggested that changing from pull ups to the diapers might help with the issue. We are going to give that a try....God bless you for caring for your FIL. So far, he is not resistant with bathing. Best to you and your family...Susan
As Alzheimer’s disease progresses, the individual’s ability to perform the activities of daily living, such as using the toilet, becomes increasingly impaired. The brain loses the ability to understand and process the steps and order in which these actions are done, and the whole process may be too overwhelming and/or confusing. Your husband’s emotional response could be in reaction to his feelings of frustration and confusion. As you and the companions for your husband have likely encountered, you will not be able to rationalize with your husband about why he needs to not only use the restroom but also why he needs to allow for some assistance. Instead, be mindful of the fear, anxiety and confusion that he may be experiencing, and approach him accordingly. Remain positive and supportive, and break down each step, offering simple verbal and visual cues. You might even want to try talking to him about something else to distract him during this time, or allow him to hold onto something comforting so he feels a sense of security while you are assisting him. Lastly, as you already do, if there is no immediate need, do not force the issue, and just try again a few minutes later.
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Thank you so much for your comments, Carol.....I failed to mention that he is already in a facility, one for memory care. I have companions with him at different times and they have asked the staff and the staff had no suggestions! When I am there I simply DO NOT FORCE the issue and try again a little later. I would not be able to do that if the problem was concerning a BM, but that has not been the case, as of yet, when I am there. So, as you can see, I need advice for me, the companions and the staff. Thanks.