Guest guest Posted June 1, 2007 Report Share Posted June 1, 2007 Hi everyone, My dad was diagnosed with LBD/vascular dementia around February of this year, but I suspect it may have been at least 2002-2003 or even earlier when symptoms appeared. He has been a diabetic (uncontrolled) for 20y or more and also hypertensive. He has diabetic retinopathy (end stage) and hasnt been allowed to drive since last year. I'm sure the diabetes was a precursor to LBD and I'm trying to keep it in check. Along with insulin and 4 BP meds, he is on Geodon 80mg bid. He was originally started on Ativan (as needed), Cogentin, Haldol(monthly) and Aricept. and progessively got worse in a span of days. he was admitted and then they stopped all meds and started back with just Geo. He was on it (Geodon) before, but was in denial about having a problem and refused to take the meds , The psych then put him on Haldol, but warned it could intensify the dementia.. which it did. He was so bad off in the hospital and the neurologist tried every test she could, but found nothing conclusive about why he deteriorated so fast. We were at a point thinking of putting him in a NH but he only had SSD and his finances were a mystery even for my mom. We're also considering having him go back to his homeland (but a nurse would have to be trained) Since he has been home he has stabilized, but his memory is still bad and he needs help with daily functions.. bathing, dressing etc. he still has some disorientation, hallucinations which mainly happen in AM My mom is ailing as well and is on O2 24/7 she cannot do more than talk to him, so I have to keep my eye on her as well. I do most of the washing, cooking, cleaning for him, so she need not worry, but it is more than I can handle. I stay with them and one of my sisters helps when she comes home in the evenings. I'm in the process of getting him mediCAL to help get a caregiver to help. I'm in the process of getting Conservatorship/DPA and I'm glad to have found this site, because i have felt so alone in this and frustrated with the system. I will say that the Caregiver resource Center has been more helpful than any social worker from the hospital yn Caregiver for Dad 71y/o in California Quote Link to comment Share on other sites More sharing options...
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