Guest guest Posted June 25, 2004 Report Share Posted June 25, 2004 Gwen, first and most importantly biggggggggggggg huggggggggg for you, and here, i will share my favorite kingsize chocolate bar, symphony with toffee chips, just melts in the mouth, mmmmmmmm i can also relate with the nh meetings, becuase i had run in with baptist skilled nursing when i asked to be present at all meetings concerning my dad, this was the day after his transfer to sn unit. well i was told the first meeting would be wed 5 days away, and that would be the goal setting meeting, i hit the ceiling the floor, the walls everything. well not literally. but my mood did, and it was very evident. i told them that goals should have been set prior to my dads admission. i was also told that it took a team to dismiss him, not just the doctors ok, but if pt/ot/rec ther/didnt feel it was right then he was gonna stay. so i said well i tell you waht this sounds more like a prison camp, and we are prisoners at your holy descretaion. i said we made a mistake, i want dr on the phone now, i am taking him home. within minutes i had supervisors everyone nearby. they all listened to me rant and rave, not that i gave them a choice. but i told them, i am to be attending all of dads medical meetings, and i expect pt to start that afternoon, that 24 hours in the unti was plenty of time to have goals set, which should have been done at discharge, etc. well fortunately they listened, they realized i have a temper and wasnt afraid of utilizing it to my and dads advantage. we were discharged 8 days later as dad had plateaued in his improving. i am glad that you got to vent and hopefully things will improve for you and others in teh nh, and i hope you can bring him home soon. my dad is 6'4 230 pounds, i am 5'6 i now after losing 30 pounds weigh 240 but due to my own medical problems ihave a 10 lb weight restriciton. so falls are very hard for us to deal with. the sn unit, concentrated on helping dad learn how to roll to get up. it takes time, but i have found that if i am caught watching him, he gets more agitated and cant do it, if he thinks he is on his own, he can do, one time it took 2 hours, usually about 30-45 minutes. dad still bathes, tho i know he is not as thorough as i would like him to be. but i just recieved the persconal care item that jim suggested, it is like a tarzan drape with velcro allowing easy access for cleaning and yet gives patient his privacy too. that might be something you should think about getting. we also spent about $500 in making the bathroom, handciapped friendly, unfortunately house was built in 1957 so bathroom door is 4 inches to narrow for walkers etc. so since dad is still able to do some walking with aids, we put a rail right inside the door, up to the tub, where opposite the tub is the sink, so he can hold on to the sink, then the toilet, where on teh wall we have a bar up at an angle. angle because you need a lower place to push up to get up and higher to hold on to as you sit down. and in the tub we have a bar on both small walls and a longer one on the main wall. and due to the fact that dad is so tall and naturallyraches u p to the shower curtain rod for support, i had it replaced with a galvanized steel rod attached at studs so now it can support his entire weight. you may consider calling a plumber and putting timers or something on the faucets to keep the overflow from happening again. like they do in public bathrooms. as for decieving your dad, you deceived the diseased part of the brain, you took care of your dad, i am learning the difference myself. dad has been very hateful to me, many times, including in his will which is in process of being drawn up. at times i am so angry but it makes me sicker so i have to vent it out, you need to as well. dont be upset that you tricked him, you did what you thought was best, and that is that. dont beat yourself up for loving and caring and wanting him safe and as healthy as can be. my dad also only gets out of bed at home to go to restroom, or go to doctor, but now that he is on exelon he practices getting up the day before he goes to doctor, that is the first time he has ever done that. i also ordered him one of those portable lift seats to see if that will help him get up easier, dont know if i can recommmend that yet, we just got it yesterday. good luck gwen, feel free to share chocolate and woes anytime!!! sharon m Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 25, 2004 Report Share Posted June 25, 2004 Gwen, you have every right to be concerned. I'd write everything down in point form and demand to have a meeting! Also, I'd write the administrator if you can't meet him/her in person. Hang in there. Courage I've had it!!!!!! >Well folks, >I think that I have had it with the total lack of communication if the elder care system! Today I went into the nursing home around 3:30 after dad would be finished with his PT. I stopped in to see the P therapist to give her information on LBD. She tells me that dad's care plan meeting was this afternoon! I know I had a shocked look on my face. If I hadn't stopped in there, I would never have known about the meeting! >I have been waiting for them to tell me when this meeting would take place. I have talked to the RNs and PT many times. I have given them LBD info and like I said in another email I've told them that I have been living with him and caring for him for 2 years. Don't ask him questions about his health, he's not going to tell you the truth. I have given them the POA and health care proxy and how could they tell someone with dementia that this meeting was taking place and think that he was going to tell me. Really! I can't believe that they would have dad in the meeting with " no representation " for him. Well by this time the people I needed to talk to had left but just wait until the morning!! I am going to have an earful for them. >I stayed with dad until about 7 p.m. After I left I decided that I needed to go to the grocery store for some CHOCOLATE ice cream. I was going through the grocery store and who do I run into? The man who staffs the local Alz. assoc. office. I knew who he was from going to several of their seminars. I introduced my self and talked for a few minutes. When I said who I was, he knew who I was because we had just talked on Mon. He was so surprized that they could hold the meeting and that I wasn't there. We also talked a few minutes about the nh and some of the things that I have observed there. He has observed some things also. > >What led up to all of this - Over the last 2 months dad has been very argumentative and telling me I was stupid etc. etc. Before that he had been fairly calm although very stubborn which is not new. >One day about 2 weeks ago dad fell and and it took about 7 hours before he could get up. When this happens he doesn't want me to help him and then I go this barrage of go away, leave me alone, I'll do it my self etc...... After he calms down, I try sitting on the floor next to him and try to guide how to move to get up, but that didn't work either. Most of dad's problem solving skills are gone. Dad was down to about 135 lbs. when I first came to live with him but through having regular meals and junk food, he is up to 170 lbs. For years that was his normal weight. I weigh about 120 lbs and am about 5 ft 1 in. There is no way that I am going to get Dad off of the floor. Anyway after about 7 hours of stuggling to get up, about 1 a.m., he finally did. The smell was pretty ripe because he had had an accident while struggling to lift his weight. I wanted to get him cleaned up and went through the barrage again. I left him alone for a while and saw that he was trying to get cleaned up. By about 3 a.m. I knew he was tiring and it might be safe for me to sleep for a while. I was in the main bathroom that I use brushing my teeth and could hear the water running in Dad's bathroom and knew that he was washing. I waited a few minutes, walked past his bedroom and found him in bed. The water was still running! Went into his bathroom and water was running everywhere as he had pulled the plunger to fill the sink! I turned off the water, went back to my room to take off pj's and put shorts back on so I could go clean up all the water all over the floor etc. >Well, the next day, I was starting to get some dinner, and went back to Dad's room to ask him something and there he is naked coming from the bathroom. He had had another accident and was just going to go back to bed (still dirty with his water was running again). I said let's get you cleaned up. Well, the barrage started again and I saw his face get white and his shaky legs get really shaky and just collapse. I thought, oh no, we ARE NOT going through this again tonight. I told him that I was going to call 911, which I did. I told them that dad had fallen and I didn't think that he was seriously hurt but I wanted him taken to the hospital to get checked out. His general condition had changed lately which I know is part of the disease, but thought that something else might be going on also. I have also learned that because I can't get him to go to the dr. when an opportunity like this presents itself, I'd better act. I hate to deceive him, but he really leaves me no choice. I talked the ER dr. into admitting him and hoping to get him checked out. I also wrote a letter for his primary to talk to him and tell him what he has and that he cannot do this by ourselves anymore. His primary has never told him what is really wrong and he refuses to see other doctors. Well, after his dr. saw him in the morning, dad was in the hospital from Tues. night in ER until Mon. morning. Luckily dad's dr. called in the neuro and they did a cat scan and thought it was NPH. On Mon. morning dad was transferred to the nh. All the while dad has been raising a stink saying that there is nothing wrong with him and he wants to go home. I hated to see him like this and it is even worse in the nh. He really needs the PT though and every day they are giving him both occupational therapy and physical therapy. He is so weak since at home he refuses to get out of bed except to go to the bathroom. >I just hate all of this but maybe I can do something with him like take him home with me. > >Sorry this has gotten so long. I think I need to go get my chocolate and prepare for the morning. >Gwen > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 25, 2004 Report Share Posted June 25, 2004 Hi My name is Jacqui. I just read you account on your Dad. I also had a fit at one of Mom's doctors. He was treating her like dirt and we switched. She is also on Exelon and it had to be increased to 4.5 mg twice a day. She takes Sequel which is 50 mg a day. The new doctor took her off Requip because it wasn't doing any good. We also have the bathroom redone with safety equip. The lift chair works great. She can't stand up from a regular chair and this one lifts her almost to a standing position. The baby monitor works for me because of my situation, but I can't see why it wouldn't work for some of you that live with your loved ones. Put in their room and the receiver can be carried around. You will be able to hear any disturbaning sounds and go see before things get too out of hand. Let's face it we are dealing with adults with childlike minds. If I sound a little harsh today, forgive me. Mom had one of her bad days and I am tired. Its only 7:00 and I have a long way to go before she settles down. Thanks for listening. Jacqui Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 25, 2004 Report Share Posted June 25, 2004 Thanks Courage, that is a good idea. When I talked to the social worker this morning he did say that they had an open door policy and call or stop by anytime I am there. I told him that I am there at least once a day. Actually I found that this was my goof. I think I am starting to loose it. When dad first arrived I signed all of the paperwork and was given a folder of papers. When I got to dad's room he was given another folder of papers. I know that I read most of the papers. While looking for the name and number of the social worker, I found a paper with the meeting date on it. To borrow Jan's phrase - shit! I am keeping a list of other things that I see though. From what I have heard around town is this nh has quite a turnover with administration and management. Hope that you are doing better and glad to see you posting occassionally. Take care, Gwen I've had it!!!!!! >Well folks, >I think that I have had it with the total lack of communication if the elder care system! Today I went into the nursing home around 3:30 after dad would be finished with his PT. I stopped in to see the P therapist to give her information on LBD. She tells me that dad's care plan meeting was this afternoon! I know I had a shocked look on my face. If I hadn't stopped in there, I would never have known about the meeting! >I have been waiting for them to tell me when this meeting would take place. I have talked to the RNs and PT many times. I have given them LBD info and like I said in another email I've told them that I have been living with him and caring for him for 2 years. Don't ask him questions about his health, he's not going to tell you the truth. I have given them the POA and health care proxy and how could they tell someone with dementia that this meeting was taking place and think that he was going to tell me. Really! I can't believe that they would have dad in the meeting with " no representation " for him. Well by this time the people I needed to talk to had left but just wait until the morning!! I am going to have an earful for them. >I stayed with dad until about 7 p.m. After I left I decided that I needed to go to the grocery store for some CHOCOLATE ice cream. I was going through the grocery store and who do I run into? The man who staffs the local Alz. assoc. office. I knew who he was from going to several of their seminars. I introduced my self and talked for a few minutes. When I said who I was, he knew who I was because we had just talked on Mon. He was so surprized that they could hold the meeting and that I wasn't there. We also talked a few minutes about the nh and some of the things that I have observed there. He has observed some things also. > >What led up to all of this - Over the last 2 months dad has been very argumentative and telling me I was stupid etc. etc. Before that he had been fairly calm although very stubborn which is not new. >One day about 2 weeks ago dad fell and and it took about 7 hours before he could get up. When this happens he doesn't want me to help him and then I go this barrage of go away, leave me alone, I'll do it my self etc...... After he calms down, I try sitting on the floor next to him and try to guide how to move to get up, but that didn't work either. Most of dad's problem solving skills are gone. Dad was down to about 135 lbs. when I first came to live with him but through having regular meals and junk food, he is up to 170 lbs. For years that was his normal weight. I weigh about 120 lbs and am about 5 ft 1 in. There is no way that I am going to get Dad off of the floor. Anyway after about 7 hours of stuggling to get up, about 1 a.m., he finally did. The smell was pretty ripe because he had had an accident while struggling to lift his weight. I wanted to get him cleaned up and went through the barrage again. I left him alone for a while and saw that he was trying to get cleaned up. By about 3 a.m. I knew he was tiring and it might be safe for me to sleep for a while. I was in the main bathroom that I use brushing my teeth and could hear the water running in Dad's bathroom and knew that he was washing. I waited a few minutes, walked past his bedroom and found him in bed. The water was still running! Went into his bathroom and water was running everywhere as he had pulled the plunger to fill the sink! I turned off the water, went back to my room to take off pj's and put shorts back on so I could go clean up all the water all over the floor etc. >Well, the next day, I was starting to get some dinner, and went back to Dad's room to ask him something and there he is naked coming from the bathroom. He had had another accident and was just going to go back to bed (still dirty with his water was running again). I said let's get you cleaned up. Well, the barrage started again and I saw his face get white and his shaky legs get really shaky and just collapse. I thought, oh no, we ARE NOT going through this again tonight. I told him that I was going to call 911, which I did. I told them that dad had fallen and I didn't think that he was seriously hurt but I wanted him taken to the hospital to get checked out. His general condition had changed lately which I know is part of the disease, but thought that something else might be going on also. I have also learned that because I can't get him to go to the dr. when an opportunity like this presents itself, I'd better act. I hate to deceive him, but he really leaves me no choice. I talked the ER dr. into admitting him and hoping to get him checked out. I also wrote a letter for his primary to talk to him and tell him what he has and that he cannot do this by ourselves anymore. His primary has never told him what is really wrong and he refuses to see other doctors. Well, after his dr. saw him in the morning, dad was in the hospital from Tues. night in ER until Mon. morning. Luckily dad's dr. called in the neuro and they did a cat scan and thought it was NPH. On Mon. morning dad was transferred to the nh. All the while dad has been raising a stink saying that there is nothing wrong with him and he wants to go home. I hated to see him like this and it is even worse in the nh. He really needs the PT though and every day they are giving him both occupational therapy and physical therapy. He is so weak since at home he refuses to get out of bed except to go to the bathroom. >I just hate all of this but maybe I can do something with him like take him home with me. > >Sorry this has gotten so long. I think I need to go get my chocolate and prepare for the morning. >Gwen > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 26, 2004 Report Share Posted June 26, 2004 Sharon, Thanks for the hugs. Never tried symphony - sounds good I'll have to try it. I found that it was my error that I missed the meeting. I got a paper with the date on it the first day, but totally missed it. I know that I read the papers but boy I missed that one. My face is red. Maybe from these conversations if caregivers have to deal with nh they will know what might be coming. What a learning experience. I talked to the social worker and he said that they have an open door policy and to call or stop by anytime. Individually I think that I have talked to all who were involved. I have been talking to them all along, except for the soc.worker. I find it very much like when the kids were in school. If you are involved and talking to the teachers they are more willing to call you if they see something. My husband told me about the nh meetings although he didn't elaborate much because he goes for his 92 yo mother in nh. Actually I called the nh where my MIL is yesterday and they have a bed for dad. I also have an AL facility that says they can take dad there. It is a continuum of care facility. These are both in Illinois. I have found that here in NY and CT (we're on the boarder) AL can't take them if they are a fall risk. The one thing that bothers me about the nh is that he has lost all of the little independence he did have left. When I am in the nh I try to help him to the bathroom so he can go sit. It is such a small thing to us but it means a lot to him. I have talked to the PT and she said that she expected about 3 to 4 weeks before he plateaus. She also told him that if he is released, that it can only be with 24 hour help/supervision. I hope that he heard that and that it got through. He doesn't realize that that is what I have been doing all this time. I was only going out about twice a week to go to the grocery store, bank, or post office and it depended on how he was doing that day. I never made appointments because it was so hard to keep them. I'm going to have to ask the PT if they have shown him how to get up when he falls. I never thought about that! When I get on the floor with him I tell him which way to roll. I try to at least get him on his knees. I don't know if that is the correct way to do it and they may have other suggestions, but lately I've had a hard time getting him to follow my direction. It really bothers me when he is on the floor for hours. I also bought the shower " pair " and was hoping that it would arrive today. Dad fussed about " they got me in the shower today " . He has an extra fear associated with the shower because several years ago he says he fell getting into the shower. That is really the only fall that he recalls. When the PT asks him if he ever falls, dad says only once. She knew the way he is so bent over that that was not true. The bad thing is in getting up or when falling he grabs for anything whether it can support his weight or not. He has also pulled out towel racks. We have done some changes but to shower he really should use the tub in the other bathroom. I got a large shower stool that fits over the side of the tub and he just has to slide over. Getting to use that is a chore too. Sigh! Thanks for your support and ideas. Gwen Re: I've had it!!!!!! Gwen, first and most importantly biggggggggggggg huggggggggg for you, and here, i will share my favorite kingsize chocolate bar, symphony with toffee chips, just melts in the mouth, mmmmmmmm i can also relate with the nh meetings, becuase i had run in with baptist skilled nursing when i asked to be present at all meetings concerning my dad, this was the day after his transfer to sn unit. well i was told the first meeting would be wed 5 days away, and that would be the goal setting meeting, i hit the ceiling the floor, the walls everything. well not literally. but my mood did, and it was very evident. i told them that goals should have been set prior to my dads admission. i was also told that it took a team to dismiss him, not just the doctors ok, but if pt/ot/rec ther/didnt feel it was right then he was gonna stay. so i said well i tell you waht this sounds more like a prison camp, and we are prisoners at your holy descretaion. i said we made a mistake, i want dr on the phone now, i am taking him home. within minutes i had supervisors everyone nearby. they all listened to me rant and rave, not that i gave them a choice. but i told them, i am to be attending all of dads medical meetings, and i expect pt to start that afternoon, that 24 hours in the unti was plenty of time to have goals set, which should have been done at discharge, etc. well fortunately they listened, they realized i have a temper and wasnt afraid of utilizing it to my and dads advantage. we were discharged 8 days later as dad had plateaued in his improving. i am glad that you got to vent and hopefully things will improve for you and others in teh nh, and i hope you can bring him home soon. my dad is 6'4 230 pounds, i am 5'6 i now after losing 30 pounds weigh 240 but due to my own medical problems ihave a 10 lb weight restriciton. so falls are very hard for us to deal with. the sn unit, concentrated on helping dad learn how to roll to get up. it takes time, but i have found that if i am caught watching him, he gets more agitated and cant do it, if he thinks he is on his own, he can do, one time it took 2 hours, usually about 30-45 minutes. dad still bathes, tho i know he is not as thorough as i would like him to be. but i just recieved the persconal care item that jim suggested, it is like a tarzan drape with velcro allowing easy access for cleaning and yet gives patient his privacy too. that might be something you should think about getting. we also spent about $500 in making the bathroom, handciapped friendly, unfortunately house was built in 1957 so bathroom door is 4 inches to narrow for walkers etc. so since dad is still able to do some walking with aids, we put a rail right inside the door, up to the tub, where opposite the tub is the sink, so he can hold on to the sink, then the toilet, where on teh wall we have a bar up at an angle. angle because you need a lower place to push up to get up and higher to hold on to as you sit down. and in the tub we have a bar on both small walls and a longer one on the main wall. and due to the fact that dad is so tall and naturallyraches u p to the shower curtain rod for support, i had it replaced with a galvanized steel rod attached at studs so now it can support his entire weight. you may consider calling a plumber and putting timers or something on the faucets to keep the overflow from happening again. like they do in public bathrooms. as for decieving your dad, you deceived the diseased part of the brain, you took care of your dad, i am learning the difference myself. dad has been very hateful to me, many times, including in his will which is in process of being drawn up. at times i am so angry but it makes me sicker so i have to vent it out, you need to as well. dont be upset that you tricked him, you did what you thought was best, and that is that. dont beat yourself up for loving and caring and wanting him safe and as healthy as can be. my dad also only gets out of bed at home to go to restroom, or go to doctor, but now that he is on exelon he practices getting up the day before he goes to doctor, that is the first time he has ever done that. i also ordered him one of those portable lift seats to see if that will help him get up easier, dont know if i can recommmend that yet, we just got it yesterday. good luck gwen, feel free to share chocolate and woes anytime!!! sharon m Quote Link to comment Share on other sites More sharing options...
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