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By proceeding, I agree that I understand the following disclosures:
I. How We Work in Washington. Based on your preferences, we provide you with information about one or more of our contracted senior living providers ("Participating Communities") and provide your Senior Living Care Information to Participating Communities. The Participating Communities may contact you directly regarding their services. APFM does not endorse or recommend any provider. It is your sole responsibility to select the appropriate care for yourself or your loved one. We work with both you and the Participating Communities in your search. We do not permit our Advisors to have an ownership interest in Participating Communities.
II. How We Are Paid. We do not charge you any fee – we are paid by the Participating Communities. Some Participating Communities pay us a percentage of the first month's standard rate for the rent and care services you select. We invoice these fees after the senior moves in.
III. When We Tour. APFM tours certain Participating Communities in Washington (typically more in metropolitan areas than in rural areas.) During the 12 month period prior to December 31, 2017, we toured 86.2% of Participating Communities with capacity for 20 or more residents.
IV. No Obligation or Commitment. You have no obligation to use or to continue to use our services. Because you pay no fee to us, you will never need to ask for a refund.
V. Complaints. Please contact our Family Feedback Line at (866) 584-7340 or ConsumerFeedback@aplaceformom.com to report any complaint. Consumers have many avenues to address a dispute with any referral service company, including the right to file a complaint with the Attorney General's office at: Consumer Protection Division, 800 5th Avenue, Ste. 2000, Seattle, 98104 or 800-551-4636.
VI. No Waiver of Your Rights. APFM does not (and may not) require or even ask consumers seeking senior housing or care services in Washington State to sign waivers of liability for losses of personal property or injury or to sign waivers of any rights established under law.I agree that: A.I authorize A Place For Mom ("APFM") to collect certain personal and contact detail information, as well as relevant health care information about me or from me about the senior family member or relative I am assisting ("Senior Living Care Information"). B.APFM may provide information to me electronically. My electronic signature on agreements and documents has the same effect as if I signed them in ink. C.APFM may send all communications to me electronically via e-mail or by access to an APFM web site. D.If I want a paper copy, I can print a copy of the Disclosures or download the Disclosures for my records. E.This E-Sign Acknowledgement and Authorization applies to these Disclosures and all future Disclosures related to APFM's services, unless I revoke my authorization. You may revoke this authorization in writing at any time (except where we have already disclosed information before receiving your revocation.) This authorization will expire after one year. F.You consent to APFM's reaching out to you using a phone system than can auto-dial numbers (we miss rotary phones, too!), but this consent is not required to use our service.
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I admitted my husband in a nursing home 2 months ago. He has vascular dementia & diabetes. He is combative at times and that was the primary reason for his admission. He had begun to hit me, resist eating and reluctant to have me change him. All that said, I see him declining even more. He has good days and bad days. I believe the drugs that he's taking for his combativeness has made him more lethargic. I miss him and want to bring him home but afraid that I will not be able to handle it. My emotions and my health are in jeopardy, I know this but I hurt for him even though I see him often and he is being taken care of. What to do is very difficult when you've been married to someone for 51 years. Everyone close to me tells me its the right thing to do but it keeps me up at night.
Welcome to the group. You didn't state why he was the nursing home. It really doesn't matter what the reason is, but if you cannot take care of him yourself, then make sure that he is being taken care of in the nursing home, visit him often (even daily if you can for dinner perhaps) and then know that he is in a secure helpful place.
See to it that he is involved in activities at the nursing home and if he is not interested in very much, make sure that he is PART of the activities, even if it is discussing his hobby to a group.
When he asks to come home, provide him with the BEST answer why he cannot: "The doctor's want you to be here with medical help, "I" cannot provide that at home, and I want you to have the best care possible! If he is aware (no dementia) this may just work. If he has dementia/Alzheimer's you will have to be more creative. I never said 'goodbye' to my mother when she was in the rehab/nursing home. I would tell her I was going to the 'store' did she need anything? I would tell her that I would be right back, just going down the hall to check on a friend, to get the mail, to get something out of my car. As you can see I would make Pinnochio look like a amateur when it came to 'creative lying' but tell the truth to my mother would only upset her, make it impossible for me to leave, or put her in a very difficult mood for the staff to have to deal with. (I couldn't spend the night there).
Be reassuring that his stay is very important to his health, but don't dwell on this 'subject'. When you visit, bring a project with you for you both to work on. It doesn't have to be too complicated, even looking through magazines for something can prove to be fun. Keep it simple, but fun.
God Bless... I hope these suggestions help. Post more information if you need more specific help.
PinkLady, your husband with Alzheimer's does not call the shots, YOU do, and you can use the same excuses or distractions or subject changers over and over again. It is sad and it is frustrating, but don't get yourself into something you cannot handle if you know you cannot handle it.
We tell my MIL - who is in Memory Care AL - that she is there for physical therapy and can come home when she is stronger and the doctor says she's ready. (She will never be coming back home - her dementia is beyond our ability to care for her and physically she is very frail - a little twig.) Moreover, she has a MUCH BETTER quality of life THERE than she did the last few months she lived with us - when she mostly stayed in her room except for meals and a very brief walk around the living room/dining room/kitchen a couple of times a day. At the AL they have a schedule of daily activities and she's not given the option of staying alone in her room for no good reason, so she gets PLENTY of healthy stimulation.
We did not and could not offer her such - as in, give up our lives entirely to "entertain" her, so she was often bored - but also refused to go out anywhere - even for a drive or to sit in the yard in good weather. Now they get her up, and into the community room, where she sits with new "friends" and participates in the activities.
Not easy, but best for all of us. I still need to make a living and am looking forward to getting back to work that I enjoy!
It probably would depend heavily upon whether your husband does have dementia/alz. Can he still be logical? If not, then that's a whole different thing. If he still has his wits about him, you tell him that you would like nothing better than to have him come home. That you wish you could turn back time to when he was well and you two were living happily together. But things have changed, you just can't do it by yourself. And if the roles were reversed, you would hope that you would be agreeable to him about that too. You are validating his feelings not dismissing them, but at the same time, things have got to stay as they are now. This is all contingent on him still having his wits about him though. And if you think he can come home for a few hours and not be miserable to have to go back, get him the heck out of there for awhile with a change of scenery. Sorry about your hubby.
PinkLady - what cstefans said. If your husband has Alzheimers, you don't have to keep thinking up new excuses - just use the old ones over and over again. He can't remember! If you need more help with this, ask the NH nurse, case manager or other appropriate staff. Helping family members deal with such issues is part of their jobs.
PinkLady, sometimes when a person has Alzheimer's/Dementia when they say "home" it usually means the home they lived in as a child.
My Dad is dealing with that with my Mom who is in long term care. I have to keep reminding him that Mom isn't talking about the house he and Mom currently own and where he is still living.... that Mom is talking about her childhood home which was a dairy farm, as I have heard her ask how are the cattle doing, which has no relationship to the houses they had owned for the past 70 years.
It's like I am dealing with two elders regarding "home", and I know how frustrating it is but more so with my Dad... as with my Mom I can say "we will go later" and she's happy with that.
I'm new to this club and am thinking there is only one answer - they have to stay there. We tell Mom she can go back to assisted living if she starts to eat and is willing to use the walker so she won't fall. That satisfies her and she promises to cooperate. Five minutes later she's forgotten the conversation but so far, going through this mantra constantly calms her down momentarily which is the best we can hope for with someone who has no short term memory. The long term memory is still there which is why she wants to go "home" but of course couldn't even tell us where that is now.
My mother says the same. At this point, home to her is the house she used to have 10 years ago. She doesn't even know where home is. Its sad. We just tell her that she is here to get stronger. We say until she starts eating better and gets strong enough to use the walker and get around she has to stay here to get help. That seems to satisfy her, although we know she will never leave the nursing home.
Its so sad when family members tell us they want to go home. It puts a lot of guilt on us, even though we know there is no option. Being old and ill, what is the first thing you want? Of course it is to be where you feel safest and most secure with the happiest memories? Home. And when dementia is part of the equation, they can't understand and rationalize why they are not home.
When Mom asked to go home, I told her yes, she could go home as soon as she is well enough which means eating better, and promised her all her furniture is at my house. That would satisfy her for the moment while I was there. (although with dementia we had that discussion several times during a visit)
The worst part was whenever I left the NH, Mom would try to get up and follow me. She was always placed in front of the nurses station so she could see me walk down the hall. When I left, she would then cry and carry on for hours because her last memory was watching me walk out without her. She would say "I'll just wait in the car, or I'll go shopping with you". I used to cry all the way out the building. We finally devised a plan with the aides who distracted her so she would not watch me physically leave. They would take her to the bathroom, or move her wheelchair into her room for a few minutes. With her short term memory pretty much gone after a few minutes, she forgot I had been there. For some reason she did remember if she watched me leave - probably because my leaving her alone had an emotional impact that stuck in her mind, whereas a quiet non-stressful visit did not.
By proceeding, I agree that I understand the following disclosures:
I. How We Work in Washington.
Based on your preferences, we provide you with information about one or more of our contracted senior living providers ("Participating Communities") and provide your Senior Living Care Information to Participating Communities. The Participating Communities may contact you directly regarding their services.
APFM does not endorse or recommend any provider. It is your sole responsibility to select the appropriate care for yourself or your loved one. We work with both you and the Participating Communities in your search. We do not permit our Advisors to have an ownership interest in Participating Communities.
II. How We Are Paid.
We do not charge you any fee – we are paid by the Participating Communities. Some Participating Communities pay us a percentage of the first month's standard rate for the rent and care services you select. We invoice these fees after the senior moves in.
III. When We Tour.
APFM tours certain Participating Communities in Washington (typically more in metropolitan areas than in rural areas.) During the 12 month period prior to December 31, 2017, we toured 86.2% of Participating Communities with capacity for 20 or more residents.
IV. No Obligation or Commitment.
You have no obligation to use or to continue to use our services. Because you pay no fee to us, you will never need to ask for a refund.
V. Complaints.
Please contact our Family Feedback Line at (866) 584-7340 or ConsumerFeedback@aplaceformom.com to report any complaint. Consumers have many avenues to address a dispute with any referral service company, including the right to file a complaint with the Attorney General's office at: Consumer Protection Division, 800 5th Avenue, Ste. 2000, Seattle, 98104 or 800-551-4636.
VI. No Waiver of Your Rights.
APFM does not (and may not) require or even ask consumers seeking senior housing or care services in Washington State to sign waivers of liability for losses of personal property or injury or to sign waivers of any rights established under law.
I agree that:
A.
I authorize A Place For Mom ("APFM") to collect certain personal and contact detail information, as well as relevant health care information about me or from me about the senior family member or relative I am assisting ("Senior Living Care Information").
B.
APFM may provide information to me electronically. My electronic signature on agreements and documents has the same effect as if I signed them in ink.
C.
APFM may send all communications to me electronically via e-mail or by access to an APFM web site.
D.
If I want a paper copy, I can print a copy of the Disclosures or download the Disclosures for my records.
E.
This E-Sign Acknowledgement and Authorization applies to these Disclosures and all future Disclosures related to APFM's services, unless I revoke my authorization. You may revoke this authorization in writing at any time (except where we have already disclosed information before receiving your revocation.) This authorization will expire after one year.
F.
You consent to APFM's reaching out to you using a phone system than can auto-dial numbers (we miss rotary phones, too!), but this consent is not required to use our service.
See to it that he is involved in activities at the nursing home and if he is not interested in very much, make sure that he is PART of the activities, even if it is discussing his hobby to a group.
When he asks to come home, provide him with the BEST answer why he cannot: "The doctor's want you to be here with medical help, "I" cannot provide that at home, and I want you to have the best care possible! If he is aware (no dementia) this may just work. If he has dementia/Alzheimer's you will have to be more creative. I never said 'goodbye' to my mother when she was in the rehab/nursing home. I would tell her I was going to the 'store' did she need anything? I would tell her that I would be right back, just going down the hall to check on a friend, to get the mail, to get something out of my car. As you can see I would make Pinnochio look like a amateur when it came to 'creative lying' but tell the truth to my mother would only upset her, make it impossible for me to leave, or put her in a very difficult mood for the staff to have to deal with. (I couldn't spend the night there).
Be reassuring that his stay is very important to his health, but don't dwell on this 'subject'. When you visit, bring a project with you for you both to work on. It doesn't have to be too complicated, even looking through magazines for something can prove to be fun. Keep it simple, but fun.
God Bless... I hope these suggestions help. Post more information if you need more specific help.
We did not and could not offer her such - as in, give up our lives entirely to "entertain" her, so she was often bored - but also refused to go out anywhere - even for a drive or to sit in the yard in good weather. Now they get her up, and into the community room, where she sits with new "friends" and participates in the activities.
Not easy, but best for all of us. I still need to make a living and am looking forward to getting back to work that I enjoy!
My Dad is dealing with that with my Mom who is in long term care. I have to keep reminding him that Mom isn't talking about the house he and Mom currently own and where he is still living.... that Mom is talking about her childhood home which was a dairy farm, as I have heard her ask how are the cattle doing, which has no relationship to the houses they had owned for the past 70 years.
It's like I am dealing with two elders regarding "home", and I know how frustrating it is but more so with my Dad... as with my Mom I can say "we will go later" and she's happy with that.
When Mom asked to go home, I told her yes, she could go home as soon as she is well enough which means eating better, and promised her all her furniture is at my house. That would satisfy her for the moment while I was there. (although with dementia we had that discussion several times during a visit)
The worst part was whenever I left the NH, Mom would try to get up and follow me. She was always placed in front of the nurses station so she could see me walk down the hall. When I left, she would then cry and carry on for hours because her last memory was watching me walk out without her. She would say "I'll just wait in the car, or I'll go shopping with you". I used to cry all the way out the building.
We finally devised a plan with the aides who distracted her so she would not watch me physically leave. They would take her to the bathroom, or move her wheelchair into her room for a few minutes. With her short term memory pretty much gone after a few minutes, she forgot I had been there.
For some reason she did remember if she watched me leave - probably because my leaving her alone had an emotional impact that stuck in her mind, whereas a quiet non-stressful visit did not.
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