Guest guest Posted September 29, 2008 Report Share Posted September 29, 2008 Hi, all. As I've written earlier, my mother was moved to the advanced unit of her facility two weeks ago. Thankfully, that transition has gone smoothly and Mom seems happy there. While spending time with Mom daily, I've noticed several of the other residents seem to display LBD tendencies. To the best of my knowledge, my mother is the first person in the unit diagnosed with LBD. At least, that's the impression I get from the staff... My question...I was told one of those residents has had " a dementia " for 15 years. I do see some LBD tendencies in her...periods where her vision is impacted, fluctuating cognition and abilities, slight slumping forward at times... Is it possible that a person could have Alzheimer's for a number of years and later develop LBD? A 15- year period seems like a long period of time even for Alzheimer's, especially when you consider that she can feed herself at times and often ask questions as well as respond to questions. I've ordered the DVD from the LBDA and will give it to the facility so they can see the symptoms first-hand. One of the care managers did tell me today that she read through the articles I had left for them. She remarked that she could see in my mother the symptoms described in the articles. This is great because their understanding can only make their job easier and Mom's life more comfortable. Thanks in advance for opinions offered. Best wishes, Lynn in Florida Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 29, 2008 Report Share Posted September 29, 2008 Yes Lynn, people can get LBD as well as Alzheimers. Also, life expectancy for PDD, when Parkinsons symptoms present well ahead of LBD, is around 13-14 years from diagnosis. Jan's Jim is around the 15 year mark I believe, but not with the dementia. So many variables to consider. I want to commend you on the very caring response you gave to Ron. It can't help but be of some comfort to him. Gibsons BC Mother died Aug. 12, 2006 at age 92 after a 13 year decline from PDD. > > Hi, all. As I've written earlier, my mother was moved to the > advanced unit of her facility two weeks ago. Thankfully, that > transition has gone smoothly and Mom seems happy there. > > While spending time with Mom daily, I've noticed several of the > other residents seem to display LBD tendencies. To the best of my > knowledge, my mother is the first person in the unit diagnosed with > LBD. At least, that's the impression I get from the staff... > > My question...I was told one of those residents has had " a dementia " > for 15 years. I do see some LBD tendencies in her...periods where > her vision is impacted, fluctuating cognition and abilities, slight > slumping forward at times... Is it possible that a person could > have Alzheimer's for a number of years and later develop LBD? A 15- > year period seems like a long period of time even for Alzheimer's, > especially when you consider that she can feed herself at times and > often ask questions as well as respond to questions. > > I've ordered the DVD from the LBDA and will give it to the facility > so they can see the symptoms first-hand. One of the care managers > did tell me today that she read through the articles I had left for > them. She remarked that she could see in my mother the symptoms > described in the articles. This is great because their > understanding can only make their job easier and Mom's life more > comfortable. > > Thanks in advance for opinions offered. > > Best wishes, > Lynn in Florida > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 30, 2008 Report Share Posted September 30, 2008 Lynn in Florida, It has been so very usual for them to call all dementias' Alzheimers. It has only been recently since the LBDA was formed and lots of info started to get out. Actually Courage started the whole letter writing campaign. She sent letters to many many many MDs and related fields. It was her private campaign for a while. Thousands of letters, wasn't it Courage? At about the same time some caregivers from here formed the LBDA and got some MDs and went to come conferences and started to talk about and educate other MDs. Six-eight years ago, you wouldn't have gotten this LBD diagnosis. Now if they would just figure out how to treat it. LOL Some MDs are doing better. 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. Question on Alzheimer's, LBD, etc. Hi, all. As I've written earlier, my mother was moved to the advanced unit of her facility two weeks ago. Thankfully, that transition has gone smoothly and Mom seems happy there. While spending time with Mom daily, I've noticed several of the other residents seem to display LBD tendencies. To the best of my knowledge, my mother is the first person in the unit diagnosed with LBD. At least, that's the impression I get from the staff... My question...I was told one of those residents has had " a dementia " for 15 years. I do see some LBD tendencies in her...periods where her vision is impacted, fluctuating cognition and abilities, slight slumping forward at times... Is it possible that a person could have Alzheimer's for a number of years and later develop LBD? A 15- year period seems like a long period of time even for Alzheimer's, especially when you consider that she can feed herself at times and often ask questions as well as respond to questions. I've ordered the DVD from the LBDA and will give it to the facility so they can see the symptoms first-hand. One of the care managers did tell me today that she read through the articles I had left for them. She remarked that she could see in my mother the symptoms described in the articles. This is great because their understanding can only make their job easier and Mom's life more comfortable. Thanks in advance for opinions offered. Best wishes, Lynn in Florida Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 30, 2008 Report Share Posted September 30, 2008 > > It has been so very usual for them to call all dementias' Alzheimers. It has only been recently since the LBDA was formed and lots of info started to get out. ***Hi, Donna and . First, thank you for your answers to my question. Perhaps this will help me when the opportunity arises to discuss the topic at the facility. *** > > Actually Courage started the whole letter writing campaign. She sent letters to many many many MDs and related fields. It was her private campaign for a while. > > Thousands of letters, wasn't it Courage? ***That's a huge undertaking! Kudos to Courage! *** > > At about the same time some caregivers from here formed the LBDA and got some MDs and went to come conferences and started to talk about and educate other MDs. ***That's wonderful! Now, I know the origin of LBDA. Thanks for sharing that bit of insight. Best wishes, Lynn in Florida Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 30, 2008 Report Share Posted September 30, 2008 > > It has been so very usual for them to call all dementias' Alzheimers. It has only been recently since the LBDA was formed and lots of info started to get out. ***Hi, Donna and . First, thank you for your answers to my question. Perhaps this will help me when the opportunity arises to discuss the topic at the facility. *** > > Actually Courage started the whole letter writing campaign. She sent letters to many many many MDs and related fields. It was her private campaign for a while. > > Thousands of letters, wasn't it Courage? ***That's a huge undertaking! Kudos to Courage! *** > > At about the same time some caregivers from here formed the LBDA and got some MDs and went to come conferences and started to talk about and educate other MDs. ***That's wonderful! Now, I know the origin of LBDA. Thanks for sharing that bit of insight. Best wishes, Lynn in Florida Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 30, 2008 Report Share Posted September 30, 2008 > > It has been so very usual for them to call all dementias' Alzheimers. It has only been recently since the LBDA was formed and lots of info started to get out. ***Hi, Donna and . First, thank you for your answers to my question. Perhaps this will help me when the opportunity arises to discuss the topic at the facility. *** > > Actually Courage started the whole letter writing campaign. She sent letters to many many many MDs and related fields. It was her private campaign for a while. > > Thousands of letters, wasn't it Courage? ***That's a huge undertaking! Kudos to Courage! *** > > At about the same time some caregivers from here formed the LBDA and got some MDs and went to come conferences and started to talk about and educate other MDs. ***That's wonderful! Now, I know the origin of LBDA. Thanks for sharing that bit of insight. Best wishes, Lynn in Florida Quote Link to comment Share on other sites More sharing options...
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