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"If she's forgetting to take her meds, it might be worth getting a dosette tray system going via her pharmacist. It won't remind her to take pills but you can tell at a glance if they've not been taken. It should be free and often includes delivery." I give her her meda as im her full time carer but 5 mins after she has taken them she will say have i got any tablets to take When you tell her she has taken them she argues you saying she not taken any | |||
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"If she's forgetting to take her meds, it might be worth getting a dosette tray system going via her pharmacist. It won't remind her to take pills but you can tell at a glance if they've not been taken. It should be free and often includes delivery. I give her her meda as im her full time carer but 5 mins after she has taken them she will say have i got any tablets to take When you tell her she has taken them she argues you saying she not taken any" This is the horrible thing about dementia. I see people swear blind they have been left all day with no food and drink when ive seen them eat all their meals. Its extremely difficult as they genuinely think that what they believe is fact and trying to convince them otherwise is usually futile. Maybe the dossette box would be better at least you could show her the empty conpartment in an attempt to reassure her? | |||
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"If she's forgetting to take her meds, it might be worth getting a dosette tray system going via her pharmacist. It won't remind her to take pills but you can tell at a glance if they've not been taken. It should be free and often includes delivery. I give her her meda as im her full time carer but 5 mins after she has taken them she will say have i got any tablets to take When you tell her she has taken them she argues you saying she not taken any" Make contact with GP, Health Visitor, Social Services and Age Concern. Are there local community volunteer organisations that will help you ? You should not have to shoulder all this on your own, no-one should ! ((((( HUG ))))) | |||
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"thing with Dementia is that its not a case of 'one size fits all' each case is very individual to that person. Some people will remain continent and be aware of toileting issues, others will forget if they have been or if they need to go. Also its vital to keep fluid uptake high, UTI's can be awful and if she forgets that she's drank she could develop them which would make the confusion even worse. Possibly start some kind of routine (before and after meals) as well as regular asking.. Can be difficult as a sole carer for your mother and it might be advisable to get a multi disciplinary team in place (GP, CPNS, Social Services and HCA's from outside care providers) to help you both. This must be an exceptionally hard time physically and mentally on yourself. Mental Capacity sounds like its been lost, but are you her named POA? Its a day by day degenerative syndrome, enjoy the good days and try to remember and reminisce over as much as you can to keep memories alive. Photographs and tresure possessions help with this, music and films too " Listen to this advice (especially about the fluid intake) as it is excellent. I have just gone through this process and I wish I had had someone to point me in the right direction. Good luck. | |||
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"Hi probably some of you might not think it appropriate to post this thread but here goes anyway. Can anyone give me advise on how to cope with caring for someone who had dimensia. My mum has it and i think its getting worse and im not coping too well. Yes she can tell me her date of birth but doesnt really remember any other dates . She dont know what day it is. Cant remember if she has had her tablets and forgets peoples names. Everyday i realise i lose a fraction more of the mum i had. Is it usual that they forget to tell you they want the loo etc? Im her full time carer but will admit its killing me and finding it hard ti cope with and as a rule im a person who is made of stone. Any advice is much appreciated " When it happened to my Nan we had no choice but to put her in a good home. It was just too much for my mum and her sisters to look after her all the time. We just made sure while she was in the home she got daily visits. | |||
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"there are better services out there that will help you cope, not only personally, but with respite and extra care/finances. google dementia care and see what it turns up. just remember you are not alone. there is brilliant support networks, and maybe even local self help groups that will be only to quick to help you in this troubling time. hope you find the help you need to aid you both" This is great advice! As a a worker in home health care in the states,the majority of my clients are to provide respite for the family! Especially when the family is with them 24/7 they need a break too. Whether its 2 ours or 8 hours there are people and support groups out there to help you the family cope. No one ever knows how difficult it until you live it. Them being incontinent is very common , reminding to bathe and take their medicines and to eat as well. What I did for one of my clients was make a book of special events that they were forgetting because certain times of the day are worse and when they are having a hard time I'd take out the book for them and go through it with them. It's not a cure by any means but with early onset dementia this is a way of helping them remember and deal with certain things. Remember they can and will get agitated and stressed out as well when there is something they just remembered hours before and it totally slips their mind. Best of luck to you! | |||
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