Early stages of dementia, crying!
7 years ago
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- 7 years ago
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My step-mother has dementia
Comments (3)I think talking to the doctor before your father (who must already be under increased stress) is a wise choice. The drug therapies for elderly dementia patients can be so individualized, the doctor may have reason for prescribing this drug given her particular history - you'll know once you've asked. All I can add is that my good friend took her mother-in-law into their home for the last 5 years of her life with dementia, very rough on the household (and mother) for the first few months with episodes of paranoia, anxiety and aggitation....which couldn't be attributed to strange surroundings, she moved from next door back into the larger family home where she had raised the son who was now 'raising' her. The neurologist prescribed Aricept and shortly after she was sleeping more hours than anyone would like to have seen, but sweet and peaceful the hours she was awake. That continued to the time of her death 4 1/2 yrs later at age 90, at home and quietly....See MoreDoes mom have dementia? Only 61
Comments (7)My grandma had dementia. She was much older, but none the less...What you're describing sounds a lot like my grandma. I was told to not neseccarily go along with what she says, but not try to argue what is "right" with her. For example, she thought the Bulgarians (whole nother story!) were after her. She was riding her bike by the train and they jumped off and threw her bike under the train. They then said they were after my dad. She was shaking and crying and telling me, begging me really, to call my dad and tell him to hide. I never in my life lied to my grandma...but I knew there was no way to reason with her...so I told her I would go call my dad immediatly. I then went to the bathroom and cried my eyes out! I gathered my strength and went back to her, told her I called my dad and he was safe. She then says "What about Bob?" (my brother). I thought fast and told her he was with dad. Whew. After that I talked to the nursing supervisor, who told me I did exactly what I should have done. Don't argue, don't reason, just nod and try to change the conversation. It was scary to go visit her as I didn't know from one day to the next how she'd be. The other thing your story reminded me of was my mom. At 60, she started forgetting things. Lots of things. Was paranoid. Acted like I was someone she didn't really like. She steadily got worse, where it was affecting my dad. One night she had a seizure, not the kind you associate with epilespy, more of a black out or fainting with a slight shake going on. She wouldn't wake up. My dad finally called 911. She "awoke" when the paramedics arrived, but didn't know who my dad was, didn't know who SHE was. She went to the hospital and they did an MRI. There was a mass in her brain. It was a brain tumor. At first they were told it was inoperable, and probably benign. After 2 yrs, she got steadily worse. She didn't remember how to spell my name. My given name. The name she gave me. She couldn't drive. She cried ALL the time. I went with to the neurologist. This time, they said they could operate. It was removed. She's gotten some of her "old self" back, but not fully. I'm not really comfortable with her as the driver. She doesn't remember from 1 day to the next something simple. Like turning on the t.v. and then turning on the DVD. Recipes. Something she's cooked forever. She now needs a recipe. Gosh, I don't mean to scare you, but have her checked. From head to toe. Terry...See MoreDementia + Sundowning
Comments (10)Hi, this is my first time on this forum. From the posts I have read, I know I will benefit from it and have a chance to laugh as I read my about life in someone else's story. I am the primary caregiver for my dad and mom, who are 87 and 85, respectively. Both suffer with dementia. My dad, however, presents the symptoms of sundowner syndrome and possibly early stages of alzheimer's. I have never known Dad to sleep for more than five or six hours before being ready to take on another day. Dad lost about 95% of his vision upon waking about a month after having a stroke five years ago. I guess within the last couple of years, Dad has had to sleep with a light so that he can get his bearings if he awakens during the night. Mom would complain and complain and complain (like your mom) about Dad getting up all through the night, and he would have no recollection of it. That would be the topic of the day-long argument. My mom likes to retire around 8:00 or 8:30 pm. and Dad still likes to wait until the 10:00 o'clock news is off. Mom forces Dad to go to bed when she's ready, and he has to comply because his sense of direction is lacking. Well, my sister (who is as restless as Dad)moved in with them for about six months. There were several occasions when Dad would get up, dress himself (often his clothes were on backward/shoes on the wrong feet), and start walking out of the door in the middle of the night. Because of his inability to see and having gone to bed so early, Dad would think it was time to get up. So, she would have to direct him back to his room and try to convince Dad to redress in his pajamas. Sometimes the only way he would go back to bed is if she would call me to come and talk to him. After my sister moved out, I moved in with them. Big mistake for my sake(I'll explain later), but I was able to understand the needs of both my parents a lot more. My dad and I have been great friends for as long as I can remember. (Mind you, I respected him as my dad, but experienced the love of my gentle giant.)During the night, my Dad continued to get up and insist on getting dressed to go outside or to work. To get someone to assist him with his clothing, Dad would also bang on the walls, windows, and/or bedposts to get our attention. We would be up two or three times per night...arguing! I would tell Dad he needed to go back to bed. He would tell me, "I'm not going back to bed, and you can't make me." Dad would get angry with me and would adamantly state that it was daytime and he needed to get up. Sometimes, Dad would even ransack his room. Usually, an hour or two had passed since he'd gone to bed. After a few words between us, he would lie down and, then, start having a conversation with himself about how badly I'd treated him. His discourse would often include, "I can't believe my own daughter would treat me that way." His "monologues" were audible, whether I was trying to sleep on the floor in the next room or on the couch in the living room. Then, he would usually go to sleep around 6:00 am and try to sleep until noon. When he arose, I would tell him about our argument, and, poor Pops had no recollection of it. I asked his doctor if it were okay to give Dad an over-the-counter sleep aid. He gladly gave me permission. Dad slept peacefully for about two nights, but the cycle of usually three consecutive nights of being up all night began again. Actually, he became more hostile when he took the sleep aid. By the way, I also tried keeping him up until at least 11:00 pm, but to no avail. Not letting him sleep in didn't stop him from staying up all night. Even changing his diet, i.e. replacing his glass of tea for dinner with water and eliminating dessert didn't help. So, while I stayed there, I had to be aware of the timing of his cycles and the patterns that would lead up to the sleepless nights. I finally had to move out for my own sake. Because I was not sleeping/resting at night and had to provide care for Dad all day with no downtime, I began to suffer with seizures and was at high risk of having a stroke. Hope this was not too long. I just want you to know you are not alone!...See MoreSevere dementia in several weeks
Comments (7)If it's the Alzheimer's form of dementia - and no way to know absolutely until an autopsy - it would be "early onset" which strikes at @65 or younger. That presents a whole different scene than deepening into the disease/condition gradually over a period of years. My Mother had Alzheimer's, but didn't present until she was into her 80's and lived to be 92. Her descent was gradual although unmistakable. She started off on Galantamine which slowed the observable things for a while - the disease was still progressing under the masking effect of the drug - then added Namenda. We stopped the Namenda since she said it made the top of her head hurt. We couldn't bear the thought of adding discomfort to what she was already going through. If there's a support group sponsored by the Alzheimer's Assn. in your area, they're quite helpful with information - especially for the caregivers, have references to available services and let you know you're not alone....See More- 7 years ago
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