Guest guest Posted July 28, 2004 Report Share Posted July 28, 2004 noted: You will find that outside of psychologist or neurologist, many physicians don't even know about LBD. ************************** Well - our doctor does not even know that much about AD. I think my mom is likely the first person he has ever seen who has dementia but I could be wrong. I do know that he listens to closely to my POA oldest sister and she really knows nothing and dismisses any of the information I send her!!! Now, sometimes, our doctor is willing to listen to what I have to say. When I told him I that my mom should be getting checkups more than once a year, he immediately agreed. Of course, my mom's six-month checkup should have been in June but my sister never made the appointment. Since my mom went into the hospital in early July with a UTI, I doubt she will be seeing our doctor until next December!!!! I did once schedule an appointment for my mother with a neurologist at the Northwestern University ADRC and forced my sister to keep the appointment but that was in November, 2001 and I doubt my mom will ever see another specialist of any stripe. It is hard when the biggest problems are caused by siblings rather than the person with dementia! As I said last night, based on the few things I have looked at so far, my mom is in the " possible LBD " category since she only has the Parkinson's symptoms so I do not know how hard I should push for her to see someone who might be able to definitively give us a diagnosis. . . carol Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 3, 2004 Report Share Posted August 3, 2004 Hi Carol, My name is Gwen and I have been 24/7 caregiver for my father for the last 2 years. I live in Naperville but have been living with my dad in New York. I have been trying to catch up on about 10 days of posts because last week I moved my dad from New York to Naperville to assisted living. I see that you are from Chicago and wanted to wish you a warm welcome. I understand about sisters!#$%. (One of the reasons that I moved dad to IL.) I guess that your sister doesn't realize that she has some of the best neurologists in the world right in Chicago! I also get digest email from the National Parkinson's foundation where they often talk about LBD. For folks in Chicago area, neurologists at Rush Presbyterian are often recommended. My husband's neurosurgeon is at Rush and I felt that he is very good. I am currently looking for a new neuro for my dad in the Naperville area to start. I have a hard time getting dad to go to any doctors but I am pushing for this now that I can just put him in the wheelchair and take him. While he was in his own home it was really hard. He had 2 flights of stairs he had to try to navigate and he has gotten to the point where he couldn't do it besides the fact that he did want to do it. My dad does not have a definite diagnosis of LBD but it was tentatively diagnosed 2 years ago. I don't remember if I saw email on any medications that your mom is taking. Is she taking any for the Parkinson's symptoms? My dad's PCP diagnosed AD and had him on lexapro and aricept. He refused to acknowledge the parkinson's symptoms. Seeing a neurologist can help to rule out many things and I for one was interested to find out what was wrong with dad's walking. The AD diagnosis just didn't feel right. Maybe this is how you are feeling. I would make an appointment with a neurologist and take your mom with or without your sister. (I've been there.) Anyway, this started out as a welcome and is getting rather long so again welcome. Gwen Re: Carol - Re: Second Opinion? noted: You will find that outside of psychologist or neurologist, many physicians don't even know about LBD. ************************** Well - our doctor does not even know that much about AD. I think my mom is likely the first person he has ever seen who has dementia but I could be wrong. I do know that he listens to closely to my POA oldest sister and she really knows nothing and dismisses any of the information I send her!!! Now, sometimes, our doctor is willing to listen to what I have to say. When I told him I that my mom should be getting checkups more than once a year, he immediately agreed. Of course, my mom's six-month checkup should have been in June but my sister never made the appointment. Since my mom went into the hospital in early July with a UTI, I doubt she will be seeing our doctor until next December!!!! I did once schedule an appointment for my mother with a neurologist at the Northwestern University ADRC and forced my sister to keep the appointment but that was in November, 2001 and I doubt my mom will ever see another specialist of any stripe. It is hard when the biggest problems are caused by siblings rather than the person with dementia! As I said last night, based on the few things I have looked at so far, my mom is in the " possible LBD " category since she only has the Parkinson's symptoms so I do not know how hard I should push for her to see someone who might be able to definitively give us a diagnosis. . . carol Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 3, 2004 Report Share Posted August 3, 2004 Gwen advised: I would make an appointment with a neurologist and take your mom with or without your sister. ******************** My mom had at test for PD while she was in the hospital a few weeks ago (with a bad asymptomatic urinary tract infection!). She tested negative for the PD but still has PD symtpoms. Last winter, for a few months, my mom was taking Amantadine when our doctor still thought she had PD but it did not help her at all. I know of some people who take Sinemet (sp) but understand this may not help either. My mom does take Exelon and Namenda among many other drugs including a diuretic and another drug for high blood pressure that was just started. She has no adverse reactions to any of her meds (I understand this can be a problem with LBD) so, for now, anyway, I guess it may not even matter exactly what dementia she has. She saw a neurologist when she was first diagnosed in 2000 and then I forced my sister to take my mom to a neurologist at the Northwestern ADRC in November of 2001. This neurologist seemed excellent (although I did not go to the appointment - another case of " if I knew then. . . " ) and he said nothing about LBD although my mom's Parkinson's-type symptoms were not as prevalent then. Anyway, I will just leave things as they are for now. If it really seems like my mom should see another neurologist, I will talk to our doctor and if he sides with my sister, and says my mom need not see another neurologist, I would, then, just take her. However, I do not want to do that unless it is absolutely necessary because the ensuing family fireworks would be catastrophic and would upset my mom. Thanks for your welcoming post. I would love to get to Naperville someday as I understand that downtown Naperville is really pretty and has a covered bridge. Then, again, I would actually rather be in NYC!!!!!! I lived there for nine years and would move back in a heartbeat if I could! carol Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 3, 2004 Report Share Posted August 3, 2004 Carol, I hear you about starting family fireworks. We do or not do things to try to keep the peace. Most of the time I function so as not to agitate dad. There were times when I didn't take dad to drs. because he had had enough with drs. For a while he had to see his primary, a gastroenterologist and urologist and when I made the appointment with the neurologist he went but said enough for going back for recheck. Now he will have a primary and hopefully a neurologist. Yes, downtown Naperville has a covered bridge. It is pretty, but getting so crowded with all of the building. When we moved to Naperville almost 30 years ago there were 26,000 people and now almost all of the farms are gone and pop. is up to 130,000. It would be nice if you could come to see it. You really would prefer NYC over the midwest? I haven't been into the city in years. Was born in the Bronx, but grew up in NJ. Dad's lived in Brewster for 30 years. It is pretty rural here, but also lots of building. Since 9/11 many people are moving out of the city. I wouldn't want to be in the city right now, especially this week with the terror alerts around Wall St. but that is just chicken me. Maybe once I get things settled for dad we can connect. Gwen Re: Carol - Re: Second Opinion? Gwen advised: I would make an appointment with a neurologist and take your mom with or without your sister. ******************** My mom had at test for PD while she was in the hospital a few weeks ago (with a bad asymptomatic urinary tract infection!). She tested negative for the PD but still has PD symtpoms. Last winter, for a few months, my mom was taking Amantadine when our doctor still thought she had PD but it did not help her at all. I know of some people who take Sinemet (sp) but understand this may not help either. My mom does take Exelon and Namenda among many other drugs including a diuretic and another drug for high blood pressure that was just started. She has no adverse reactions to any of her meds (I understand this can be a problem with LBD) so, for now, anyway, I guess it may not even matter exactly what dementia she has. She saw a neurologist when she was first diagnosed in 2000 and then I forced my sister to take my mom to a neurologist at the Northwestern ADRC in November of 2001. This neurologist seemed excellent (although I did not go to the appointment - another case of " if I knew then. . . " ) and he said nothing about LBD although my mom's Parkinson's-type symptoms were not as prevalent then. Anyway, I will just leave things as they are for now. If it really seems like my mom should see another neurologist, I will talk to our doctor and if he sides with my sister, and says my mom need not see another neurologist, I would, then, just take her. However, I do not want to do that unless it is absolutely necessary because the ensuing family fireworks would be catastrophic and would upset my mom. Thanks for your welcoming post. I would love to get to Naperville someday as I understand that downtown Naperville is really pretty and has a covered bridge. Then, again, I would actually rather be in NYC!!!!!! I lived there for nine years and would move back in a heartbeat if I could! carol Welcome to LBDcaregivers. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 3, 2004 Report Share Posted August 3, 2004 Gwen - Naperville is now the second or third (I forget which) largest municipality in Illinois!!! Pretty amazing!!! I have never heard of Brewster - well I have heard of Mortimer Brewster and his Brewster aunts from " Arsenic and Old Lace " !!! I try to keep peace in the family but when things have to be done, I make sure that they are!!! take care - carol Quote Link to comment Share on other sites More sharing options...
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