Guest guest Posted June 9, 2011 Report Share Posted June 9, 2011 Hi - is it Jane? You did not mention your name but the e-mail addy looks like that might be it. Please know - YOU are not alone. I'm so glad your father is in a facility where he's safe and cared for - my dad is, too. I hope you take time for yourself. Quiet time is not time taken away from your parents, it's something you deserve, and an investment in the long-term. I'm not a medical person at all, but just reading your e-mail I wonder if perhaps your mother's forgetfulness is from stress, rather than Alzheimer's. Only a doctor can sort that out, though. I will pray that the social worker is great and gives you some good support! Ellen in OH ________________________________ To: LBDcaregivers Sent: Thu, June 9, 2011 8:07:10 AM Subject: just need to talk/post  Dad is at a long term care facility in personal care - not a dementia unit which is very good. He has many many friends and plays cards and does have a good personality - he appears to have adjusted well at least in the eyes of the staff and I truly believe he has. This month he's been angry at all of us and I beleive it's justifiable. He wants Mom to move in now. But she's not ready. He says people ask about his wife everyday and it makes everything awful. Mom will only visit 1 day a week becuase that's all she can tolerate. Dad calls Mom all the time and just yells at her and tries to force her to move there or visit more often that will not happen because the relationship has become so strained. Mom is tired of giving in I understand that and I support that. I also understand that Dad wants to see her more often. We are going to meet with the social worker at the nursing home. I don't know what to do for either one of them any longer. I let Mom listen into the conversation I had with Dad last night. He insisted that the marrage was over. I said no it's not. He said he was abandon. You are there because you need full time nursing care. Mom is not a nurse, I'm not a nurse and my sister is not a nurse. The dementia has really gotten a grip on you and we don't know what to do any more. This happens everyday around 3 pm so I know it's associated with sundowners. I know my sister has had it will me. I understand that as well. I know there is absolutley nothing else I can do. I am no longer a comfort to anyone in the family anymore and I am not communicating effectively with any of them. I wonder if I ever will be able to. I cannot answer all of Mom questions or Dad's questions when I do answer them I don't give them the answers they want or the answers are just not good enough. I have no skills in psychology or generontology. I know there is nothing you folks can do. but having the abilty to just post this does help. My heart goes out to all of you who have loved ones at home who are dealing with LBD on a daily basis. It finally got the best of us and I know that Dad is in very very good hands. I'm not sure medicating him is the right thing - I'm not even sure there is a right or wrong thing. Again all my best to those of you with loved ones at home living with you. Thank you for just letting me get this out. I know I'm going to have to get better at coping. I wish I could be of more assistance to my parents and sister but I'm just failing misrebly. I know Mom feels the same way she said I just feel like I'm in a hole and I can't get out. I know that the hole is the fact DAd has dementia and nobody can get out. On top of that I feel that she has started exhibiting signs of Altzhiemers. Loosing words, in ability to balance a checkbook, not being able to keep things straight when she's given instructions over the phone. I know she's not ready to acknowledge the fact she may have this. If we could get a few months of calm she might be able to accept her own problems but right now she just will not. Again thank you for letting me get this out. I know there is nothing any of you can do and I know most of you are experiencing much worse. My heart goes out to all of you. You are not alone. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 9, 2011 Report Share Posted June 9, 2011 Jane, " ... He wants Mom to move in now. But she's not ready. He says people ask about his wife everyday and it makes everything awful. Mom will only visit 1 day a week becuase that's all she can tolerate. > " > We are going to meet with the social worker at the nursing home. I don't know what to do for either one of them any longer. . I know my sister has had it will me. I understand that as well. I know there is absolutley nothing else I can do. I am no longer a comfort to anyone in the family anymore and I am not communicating effectively with any of them. " Don't blame yourself. The situation is impossible. No one can deal rationally with irrational demands. All the choices in front of you are bad. But you can find support, possibly through your church, a social worker, or some trained in psychology. And you should, because you deserve it. You're trying hard to resolve irreconcilable differences and even if your parents don't recognized it because their mental states won't allow them to understand, you are their best support. For their sakes and for your own, find someone who will listen and tell you that you can only do your best, you can't magically reverse this tragic decline in both your parents. Best regards, Ann Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 9, 2011 Report Share Posted June 9, 2011 Hi Jane, I might be coming into this late; I've been rather busy lately so have only been able to skim emails. But I do have some questions or ideas for you to ponder, if nobody has asked them yet. How long has your dad been in the facility? Is he on no medication? (Something you said made it sound that way.) There is clearly a lot of strain going on for all of you. Part of the problem of course with him not being in a dementia unit is that his caregivers might not know exactly what to look for, how to respond to issues, when to suggest medications, etc. I understand why you're happy he is not in a dementia unit, but that isn't necessarily all good. Is he involved with a neurologist and psychiatrist? Apparently he's been diagnosed with LBD from the sounds of it. Again, I apologize if I am repeating questions that others have asked...I've been absent. My other thought, and I am a master's level psychotherapist, is that I'm wondering if your mom is necessarily exhibiting signs of Alzheimer's, or if it might be a stress response. You may be right in your assessment, but just remember that the level of stress from dealing with this and facing his anger and feeling in a hole like she does CAN account for all the symptoms you're seeing as well. That was just something I wanted to pass on for you to ponder. Best of luck with what you're dealing with. You, too are not alone, and the stress you're under is real, whether it seems like others have 'worse' situations or not. Lori just need to talk/post Dad is at a long term care facility in personal care - not a dementia unit which is very good. He has many many friends and plays cards and does have a good personality - he appears to have adjusted well at least in the eyes of the staff and I truly believe he has. This month he's been angry at all of us and I beleive it's justifiable. He wants Mom to move in now. But she's not ready. He says people ask about his wife everyday and it makes everything awful. Mom will only visit 1 day a week becuase that's all she can tolerate. Dad calls Mom all the time and just yells at her and tries to force her to move there or visit more often that will not happen because the relationship has become so strained. Mom is tired of giving in I understand that and I support that. I also understand that Dad wants to see her more often. We are going to meet with the social worker at the nursing home. I don't know what to do for either one of them any longer. I let Mom listen into the conversation I had with Dad last night. He insisted that the marrage was over. I said no it's not. He said he was abandon. You are there because you need full time nursing care. Mom is not a nurse, I'm not a nurse and my sister is not a nurse. The dementia has really gotten a grip on you and we don't know what to do any more. This happens everyday around 3 pm so I know it's associated with sundowners. I know my sister has had it will me. I understand that as well. I know there is absolutley nothing else I can do. I am no longer a comfort to anyone in the family anymore and I am not communicating effectively with any of them. I wonder if I ever will be able to. I cannot answer all of Mom questions or Dad's questions when I do answer them I don't give them the answers they want or the answers are just not good enough. I have no skills in psychology or generontology. I know there is nothing you folks can do. but having the abilty to just post this does help. My heart goes out to all of you who have loved ones at home who are dealing with LBD on a daily basis. It finally got the best of us and I know that Dad is in very very good hands. I'm not sure medicating him is the right thing - I'm not even sure there is a right or wrong thing. Again all my best to those of you with loved ones at home living with you. Thank you for just letting me get this out. I know I'm going to have to get better at coping. I wish I could be of more assistance to my parents and sister but I'm just failing misrebly. I know Mom feels the same way she said I just feel like I'm in a hole and I can't get out. I know that the hole is the fact DAd has dementia and nobody can get out. On top of that I feel that she has started exhibiting signs of Altzhiemers. Loosing words, in ability to balance a checkbook, not being able to keep things straight when she's given instructions over the phone. I know she's not ready to acknowledge the fact she may have this. If we could get a few months of calm she might be able to accept her own problems but right now she just will not. Again thank you for letting me get this out. I know there is nothing any of you can do and I know most of you are experiencing much worse. My heart goes out to all of you. You are not alone. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 19, 2011 Report Share Posted June 19, 2011 Jane, I know I am late in answering your message, but I wanted to tell you, you may want your Mom to see her MD. He may be able to help with meds for the stress or something. She could be just so stressed nothing will help until she isn't as stressed. Just my thought, Hugs, Donna R Cared for Mom 3 years in my home and the last year at a nh. She passed away from LBD in 2002. just need to talk/post Dad is at a long term care facility in personal care - not a dementia unit which is very good. He has many many friends and plays cards and does have a good personality - he appears to have adjusted well at least in the eyes of the staff and I truly believe he has. This month he's been angry at all of us and I beleive it's justifiable. He wants Mom to move in now. But she's not ready. He says people ask about his wife everyday and it makes everything awful. Mom will only visit 1 day a week becuase that's all she can tolerate. Dad calls Mom all the time and just yells at her and tries to force her to move there or visit more often that will not happen because the relationship has become so strained. Mom is tired of giving in I understand that and I support that. I also understand that Dad wants to see her more often. We are going to meet with the social worker at the nursing home. I don't know what to do for either one of them any longer. I let Mom listen into the conversation I had with Dad last night. He insisted that the marrage was over. I said no it's not. He said he was abandon. You are there because you need full time nursing care. Mom is not a nurse, I'm not a nurse and my sister is not a nurse. The dementia has really gotten a grip on you and we don't know what to do any more. This happens everyday around 3 pm so I know it's associated with sundowners. I know my sister has had it will me. I understand that as well. I know there is absolutley nothing else I can do. I am no longer a comfort to anyone in the family anymore and I am not communicating effectively with any of them. I wonder if I ever will be able to. I cannot answer all of Mom questions or Dad's questions when I do answer them I don't give them the answers they want or the answers are just not good enough. I have no skills in psychology or generontology. I know there is nothing you folks can do. but having the abilty to just post this does help. My heart goes out to all of you who have loved ones at home who are dealing with LBD on a daily basis. It finally got the best of us and I know that Dad is in very very good hands. I'm not sure medicating him is the right thing - I'm not even sure there is a right or wrong thing. Again all my best to those of you with loved ones at home living with you. Thank you for just letting me get this out. I know I'm going to have to get better at coping. I wish I could be of more assistance to my parents and sister but I'm just failing misrebly. I know Mom feels the same way she said I just feel like I'm in a hole and I can't get out. I know that the hole is the fact DAd has dementia and nobody can get out. On top of that I feel that she has started exhibiting signs of Altzhiemers. Loosing words, in ability to balance a checkbook, not being able to keep things straight when she's given instructions over the phone. I know she's not ready to acknowledge the fact she may have this. If we could get a few months of calm she might be able to accept her own problems but right now she just will not. Again thank you for letting me get this out. I know there is nothing any of you can do and I know most of you are experiencing much worse. My heart goes out to all of you. You are not alone. Quote Link to comment Share on other sites More sharing options...
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