Guest guest Posted June 9, 2007 Report Share Posted June 9, 2007 Hey all it been a long while since i wrote , or even logged on into my email account. i ve been crazy busy between work and trying to settle things down at home( ie finding extra help, finding a local neurologist, physiotherapest... etc) Ive managed to find a great physiotherapest that has been coming over 3 times a week , he's had experience with people with alzheimers and he workd great with my mother and shes very responsive and the most alert i see her all day when shes doing her routine with him. Other than that ,I was talking to my cousin on the phone and we were thinking back as to how my moms deterioration has been speeding up. Is this normal ? i mean just a month ago she used to go out walking and take cabs on her own. Lately shes been in her own world , contstantly entertaining popele who don exist at home. The music is on 24/ 7 and shes ALWAYS singing and dancing . sometimes she'll even dress up. Shes always standing by the window and shouting out all sorts of things ( luckily i havent heard any complaints from the neighbours, eventhough we've always had differences with them). Yesterday was the first time we were able to take her outside the house, although it was super tough. We took her to my sisters house for lunch. My mom was screaming the whole way and kept saying that she has so many " appointments " to attend to. anyway once we got there , we put on some music , she danced and sang like she does at home, she ate well then eventually became restless and insisted that she wanted to go home. Not only that , her behaviour is becoming alot like achild, she cannot take showers on her own ( this development is very recent) yesterday i found out that our housekeeper has been bathing her for the past week. It was so shocking to see my mom sitting in thge bath tub , playing and splashing around for almost an hour. Its so ironic because my mother was always a woman on the run , ultra quick morning showers and off to run errands back in time to cook lunch for the whole house. Its also ironic in how she thinks shes always entertaining people because thats alot like the social butterfly she use to be in the past , she was a great cook and we constantly had her friends and relatives over. Unfortunately these days my moms friends dont call her anymore and the number of relatibves we have locally- that care- are very few. In any case , she hardly sits with anyone that comes to visit her , shell leave them sitting in the living room and go inside her room and just dance away to loud music. I know the deterioration to be expected of LBD , Ive read so much about it, but is it supposed to decline to quickly? For the past month ive been experiencing one shock after the other in my mothers condition , I just wish things could just stabalize so that I can have some time to breath and get ready for the coming stages.... you know what i mean??? any chance of that happenening? im taking my mom for some blood tests and a urine test to get her checked out by her neurologist. Well i better run now , just thought id give you all an update on my mom and me Nina Mother 61 with LBD - diagnosed last year (Sept 2006) --------------------------------- Be a better Globetrotter. Get better travel answers from someone who knows. Yahoo! Answers - Check it out. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 9, 2007 Report Share Posted June 9, 2007 Hi Nina. Thanks for the update. That's what we experienced with my mother - before we could even grasp one symptom another would show up. That's why LBD is so different (and sometimes more difficult) than ALZ. The rapidity of it. It's probably not what you want to hear -- but I think it's great that your mom is singing and dancing. Sometimes their reality is so much better than our reality. I'd just go with it... I'd be dancing & singing along with her! LOL Have you considered getting companions to be her 'guests' -- to be part of her reality? You've found a wonderful housekeeper who cares enough to give your mom a bath -- a keeper to say the least. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 9, 2007 Report Share Posted June 9, 2007 Hey Thanks for your email , im definately holding on to the house keeper!! Ive interviewed so many nurses but none of them would really click with my mom as a companion- personality wise- but we're still searching , that is actually the most difficult to find! Nina wrote: Hi Nina. Thanks for the update. That's what we experienced with my mother - before we could even grasp one symptom another would show up. That's why LBD is so different (and sometimes more difficult) than ALZ. The rapidity of it. It's probably not what you want to hear -- but I think it's great that your mom is singing and dancing. Sometimes their reality is so much better than our reality. I'd just go with it... I'd be dancing & singing along with her! LOL Have you considered getting companions to be her 'guests' -- to be part of her reality? You've found a wonderful housekeeper who cares enough to give your mom a bath -- a keeper to say the least. Welcome to LBDcaregivers. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 9, 2007 Report Share Posted June 9, 2007 Nina, I don't happen to believe it is good for your Mom to just be home alone. When I had Mom and she got like that is when I put her in day care. It gave her somewhere to go and be with people who were " like " her. Once she started going, ( and I bet you could make it one of her " appointments " ) you might find more time and more hands to help. They do the singing and tossing the ball and lots of things to stimulate their minds. That would solve your problem of no time and also give her some things to do to structure her time and be with people. And I do know how all those " friends " disappear. Hope you would give this some thought. Hugs, Donna R Caregave for Mom (after I brought her from WI to MI) for 3 years and 4th year in a nh. She was almost 89 when she died in '02. No dx other than mine. Speedy Deterioration Hey all it been a long while since i wrote , or even logged on into my email account. i ve been crazy busy between work and trying to settle things down at home( ie finding extra help, finding a local neurologist, physiotherapest... etc) Ive managed to find a great physiotherapest that has been coming over 3 times a week , he's had experience with people with alzheimers and he workd great with my mother and shes very responsive and the most alert i see her all day when shes doing her routine with him. Other than that ,I was talking to my cousin on the phone and we were thinking back as to how my moms deterioration has been speeding up. Is this normal ? i mean just a month ago she used to go out walking and take cabs on her own. Lately shes been in her own world , contstantly entertaining popele who don exist at home. The music is on 24/ 7 and shes ALWAYS singing and dancing . sometimes she'll even dress up. Shes always standing by the window and shouting out all sorts of things ( luckily i havent heard any complaints from the neighbours, eventhough we've always had differences with them). Yesterday was the first time we were able to take her outside the house, although it was super tough. We took her to my sisters house for lunch. My mom was screaming the whole way and kept saying that she has so many " appointments " to attend to. anyway once we got there , we put on some music , she danced and sang like she does at home, she ate well then eventually became restless and insisted that she wanted to go home. Not only that , her behaviour is becoming alot like achild, she cannot take showers on her own ( this development is very recent) yesterday i found out that our housekeeper has been bathing her for the past week. It was so shocking to see my mom sitting in thge bath tub , playing and splashing around for almost an hour. Its so ironic because my mother was always a woman on the run , ultra quick morning showers and off to run errands back in time to cook lunch for the whole house. Its also ironic in how she thinks shes always entertaining people because thats alot like the social butterfly she use to be in the past , she was a great cook and we constantly had her friends and relatives over. Unfortunately these days my moms friends dont call her anymore and the number of relatibves we have locally- that care- are very few. In any case , she hardly sits with anyone that comes to visit her , shell leave them sitting in the living room and go inside her room and just dance away to loud music. I know the deterioration to be expected of LBD , Ive read so much about it, but is it supposed to decline to quickly? For the past month ive been experiencing one shock after the other in my mothers condition , I just wish things could just stabalize so that I can have some time to breath and get ready for the coming stages.... you know what i mean??? any chance of that happenening? im taking my mom for some blood tests and a urine test to get her checked out by her neurologist. Well i better run now , just thought id give you all an update on my mom and me Nina Mother 61 with LBD - diagnosed last year (Sept 2006) --------------------------------- Be a better Globetrotter. Get better travel answers from someone who knows. Yahoo! Answers - Check it out. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 10, 2007 Report Share Posted June 10, 2007 nina, first i am glad that your mom is happy and dancing and singing. that is wonderful, as when my dad deteriorated quickly he became more aggressive verbally and emotionally to me. my dads progreesion of the disease slowed on exelon but after he had his hip surgery his decline was very very fast. please enjoy the singing and dancing, she is happy even if it iin her own litle world and as for bathing, you may want to cut down her bahts to every few days, unless she really needs a bath why give her one. until dad was messing on himself hospice would only come 2 times a week to bathe him but after he lost contorl of bowels and bladder it was then a daily thingl and all of dads friends disappeared when we moved down, it was like they didnt care anymore, fortuantly my best friend jennie cared adn came to visit dady and when i needed a break came and took care of daddy, she lost her dad 3 years before and she would say he was her adoped dad. it was great. hugs, sharon ---- Nina Jordan wrote: Hey all it been a long while since i wrote , or even logged on into my email account. i ve been crazy busy between work and trying to settle things down at home( ie finding extra help, finding a local neurologist, physiotherapest... etc) Ive managed to find a great physiotherapest that has been coming over 3 times a week , he's had experience with people with alzheimers and he workd great with my mother and shes very responsive and the most alert i see her all day when shes doing her routine with him. Other than that ,I was talking to my cousin on the phone and we were thinking back as to how my moms deterioration has been speeding up. Is this normal ? i mean just a month ago she used to go out walking and take cabs on her own. Lately shes been in her own world , contstantly entertaining popele who don exist at home. The music is on 24/ 7 and shes ALWAYS singing and dancing . sometimes she'll even dress up. Shes always standing by the window and shouting out all sorts of things ( luckily i havent heard any complaints from the neighbours, eventhough we've always had differences with them). Yesterday was the first time we were able to take her outside the house, although it was super tough. We took her to my sisters house for lunch. My mom was screaming the whole way and kept saying that she has so many " appointments " to attend to. anyway once we got there , we put on some music , she danced and sang like she does at home, she ate well then eventually became restless and insisted that she wanted to go home. Not only that , her behaviour is becoming alot like achild, she cannot take showers on her own ( this development is very recent) yesterday i found out that our housekeeper has been bathing her for the past week. It was so shocking to see my mom sitting in thge bath tub , playing and splashing around for almost an hour. Its so ironic because my mother was always a woman on the run , ultra quick morning showers and off to run errands back in time to cook lunch for the whole house. Its also ironic in how she thinks shes always entertaining people because thats alot like the social butterfly she use to be in the past , she was a great cook and we constantly had her friends and relatives over. Unfortunately these days my moms friends dont call her anymore and the number of relatibves we have locally- that care- are very few. In any case , she hardly sits with anyone that comes to visit her , shell leave them sitting in the living room and go inside her room and just dance away to loud music. I know the deterioration to be expected of LBD , Ive read so much about it, but is it supposed to decline to quickly? For the past month ive been experiencing one shock after the other in my mothers condition , I just wish things could just stabalize so that I can have some time to breath and get ready for the coming stages.... you know what i mean??? any chance of that happenening? im taking my mom for some blood tests and a urine test to get her checked out by her neurologist. Well i better run now , just thought id give you all an update on my mom and me Nina Mother 61 with LBD - diagnosed last year (Sept 2006) --------------------------------- Be a better Globetrotter. Get better travel answers from someone who knows. Yahoo! Answers - Check it out. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 11, 2007 Report Share Posted June 11, 2007 Thanks and Sharon I think the closest Alzeimers Association to me would be the one in Lebanon. Do you think they are worth contacting even if they're not available locally? Today I was going to have the lab come over and have my mom do blood and urine tests but she resisted today and she got really furious , although yesterday she was ok with it. Is there a certain way of going arouns this besides getting the lab to come over so that my mom can do it at the comfort of her own home? Sharon , rigth now im sort of appreciating the fact that shes been in a good mood in her own little world , especially when she was very agressive towards me and the whole family for a whole month last month . I think one of the most difficult things about LBD is waking up everyday not knowing what to expect from you LO, atleast thats how things have been on my side with my mom , everyday .... theres no stability at all. Nina wrote: I think you told us that and I had forgotten. Do you have an Alzheimers Association there? Nina Here's a page that lists the international Alz. Assoc. -- any of them near you? or at least they can direct you to help in your area? http://www.alz.co.uk/help/associations.html http://www.alz.co.uk/ Welcome to LBDcaregivers. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 11, 2007 Report Share Posted June 11, 2007 <snip> I think the closest Alzeimers Association to me would be the one in Lebanon. Do you think they are worth contacting even if they're not available locally? <snip> I think so -- they may know of specialists in your area that can help you, if nothing else they may have some suggestions for you. <snip> Today I was going to have the lab come over and have my mom do blood and urine tests but she resisted today and she got really furious , although yesterday she was ok with it. Is there a certain way of going arouns this besides getting the lab to come over so that my mom can do it at the comfort of her own home? <snip> talked about working with the lab -- their providing you with what you need to get samples and then your taking them to the lab. That might work - read here: http://health.groups.yahoo.com/group/LBDcaregivers/message/61569 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 11, 2007 Report Share Posted June 11, 2007 Nina, for the labs, if you are talking about urine tests you can get teh cups and wipes to clean her before catching her pee, does seh still go to teh abathroom if so the lab adn give you a hat, it fit between teh toilet and the toilet seat, it catches urine and then you can pour to fill up your collection cup. if she doesnt, that might be a problem unless you can time it for when she is peeing as you dont want anything form contaminated diapers or depends. then they would want to cathetize her, caths are difficult for the patient, it is very uncomfortable even hurts and for someone with dementia issues very scary and makes it worse. please let me know some answers and we can see if between teh group we can come up with plan a or b for you, good luck and hugs, sharon ---- Nina Jordan wrote: Thanks and Sharon I think the closest Alzeimers Association to me would be the one in Lebanon. Do you think they are worth contacting even if they're not available locally? Today I was going to have the lab come over and have my mom do blood and urine tests but she resisted today and she got really furious , although yesterday she was ok with it. Is there a certain way of going arouns this besides getting the lab to come over so that my mom can do it at the comfort of her own home? Sharon , rigth now im sort of appreciating the fact that shes been in a good mood in her own little world , especially when she was very agressive towards me and the whole family for a whole month last month . I think one of the most difficult things about LBD is waking up everyday not knowing what to expect from you LO, atleast thats how things have been on my side with my mom , everyday .... theres no stability at all. Nina wrote: I think you told us that and I had forgotten. Do you have an Alzheimers Association there? Nina Here's a page that lists the international Alz. Assoc. -- any of them near you? or at least they can direct you to help in your area? http://www.alz.co.uk/help/associations.html http://www.alz.co.uk/ Welcome to LBDcaregivers. Quote Link to comment Share on other sites More sharing options...
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