I am the care giver of my 86 yr old mother. I work full time and her dementia was keeping me up at night. I was so pleased when the local psychologist told me we could her have her evaluated at a geriatric psychiatrirc inpatient unit (5-20 day stay) to get help with her sporadic sleep. Prior to this admission, she would get up in the morning, wash and dress herself, I would feed her breakfast then put her on her Senior Center bus. She would spend a few hours at the center having lunch and being with friends, ride the bus home where a relative would stay with her until I got off work. She was admitted and it is now six weeks later and she is still at the hospital psych unit. Since admission there has been a rapid decline in her physical and mental health. They keep her tied up to a recliner-like chair, she no longer walks, although she walked in the day of admission. Her period of lucid thoughts are very rare, she usually makes no sense when tyring to converse with her. She now keeps her eyes closed 95 % of the time, the doctor has no explanation for this. She keeps both hands in a clenched fist position and can no longer feed herself, She has lost a lot of weight. There has been liltle to no change in her sleep patterns, which was the inital reason for the admission. She has had to be sedatated on occassion for severe agitation. She crys a lot and calls out to deceased relatives often. I feel so guilty for putting her there, my intentions were good yet it has only turned out to be a nightmare. I am an emotional wreck feeling like I made choices that caused harm to the person I love the most, I miss her so much. I cannot believe how rapidly she declined, we are now looking into hopsice and nursing home care. Does any one have any insight?
I sincerely feel she is forcing her body to remain alive through fear and pays for it through her mental pain.
Learn that it is not your pain, it is hers to bear. And she will, until it's time for her to go. That is true love.
Prayers to you both.
Is there any nursing home closer to where you live? I have found it much easier to get what I want, and to get something that works better for my brother, when I thought about what would not just work, but would be nice, and looked around, and had a place in mind with reasons for it. Now that I'm older, I find it too tiring to do all the travel - before I set him up so he could develop his life where he is, but now, it's hard for me to see him with a 5 hour trip. If it was a parent, I think I might look into something closer to me, for many of them are similar - and sometimes episodes happen with some staff - some staff don't back down, and sometimes they should. But if it takes all those meds to keep your mom calm, then can you at least bring her near you, so you can visit, and plan to sort out many of these issues over the next 2 years or so? That could let you sort things out, while still visiting your mom, maybe 2 days a week? An hour and a half at a time? Too often we try to be ALL to them, instead of making it easy for ourselves to stay in touch. I wish you luck, but I really do think that if you and your husband found an alternative, they might be glad to let you take her. And if you talk with any new home, you can say, she is usually calm, it just helps if people make a list of her needs, or maybe what upsets her, and pay attention - then she's a model patient. You can sell it!
Mom was screaming when she was at the other nursing home out of state that I moved her from. She was getting the antipsychotic, other anxiety and anti depressants when there. When the screaming started back up, they suggested the pysch hospital because they didn't know where to go next as far as the meds go. I have a feeling that making her take a shower and going to bed with wet hair may have caused it to get out of hand. I can remember her always telling me as a child, not to go to bed with wet hair. :) She didn't like the showers to begin with and wanted sponged baths instead. She really flipped when they made her take one and go to bed in the evening with wet hair. They said they had a towel on her pillow. I usually could calm her down and get her to tell me what it was she needed, like water, etc. The screaming became non stop and that's why they suggested the pysch hospital. Wrong move I made. As I said before, it may her worse and not eating on top of that. Before she drank plently of water and always ate very good.
I know how you feel as I am in the same boat! I have POA over my mother. I was advised by the nursing home that my mom's screaming was out of control and that she needed to be admitted to a pysch hospital for evaluation and see if they can find treatment to stop the yelling. She has gone down hill since! She has only been there almost 2 weeks and has already falling out of her wheelchair, another time had a busted upper right lip and today she has a busted lower left lip. The nurse today was already on the defense when I asked about it. And my husband stepped in. She didn't like that and said that we both had to leave! As we were arguing with her and should not be doing that in front of my mom. We were not arguing with her. I let the RN and another nurse know that I had the right to ask what happened and if it had been their mother they would've done the same. I told them I had no problem of moving her to another hospital. I still might just do that. When she had the fall out of the wheelchair, it could've killed her. She landed on her forehead and knees. It just seems she is kept drugged up and that is not what I wanted. My mom always ate real good in the past. But since she's been there her appetite is declining. They did take her off the antipsychotic medicine as I requested. I hope they were telling me the truth. They still have her on Xanax and Prozac and I'm beginning to wonder if she should be off of these as well.
Antipsychotic meds can cause drug-induced parkinsonism and other movement disorders. I don't necessarily think every drug on the Beers list is absolutely contraindicated for every elederly person in every situation, but side effects have to be considered. I'm hoping you have medical POA so you can get her out and get meds revised. If not, you could make reports to the local ombudsman and/or suggest subtly that you would consider taking legal action and that might encourage them to want her out.
People with dementia do decline. Sometimes the declines are abrupt and steep. Perhaps Mom would have had a drastic decline even if she had stayed home. I don't suppose you'll ever know. Know this, though: this is Not Your Fault.
Hugs to you and to your dear mother.