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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.
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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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He gets sad any time I even mention going visit. I feel he needs to go talk to someone to learn how to deal with feelings but he feels it would not help. I don’t know how to help.
So very sorry for both of you. Ask him to list 5 issues/problems he has with mom. Then, number them in order of the hardest part to the least problematic. First step in figuring out what the person's (or your own) problems are is by knowing them. Just blurting it out isn't an option for some because they're not sure themselves. Writing it down makes it solid and gives you something to guage his most stressful issues by. Keeps the focus on improvement and just discuss one problem at a time with a plan to make it work. Coping out is not a option.
It must be hard worrying about what part of Mom will still be there when you visit. I think that bothered my husband when we visited his dad. The man he knew all his life was no longer there and had lost his independence. Maybe too some worry about “is this my future”? It was easier for me he wasn’t my Dad but I had known him for over 30 years and oddly enough I was the one he always knew when we visited and I’d get the biggest smile from him. I think hubby also tried to look for a conversation that was current but Dad was often in another time. I tried to just let him tell us what was going on in his thoughts and then reassure him things would work out. Often he worried about finding a new job or where he was going to live. A simple we can talk about that when we need to or that there was enough of us that he would always have a place to live seemed to help.
He is grieving the loss of the mother he knows and loves. He should talk with a counsellor, a pastor, or a group dealing with loss.
My husband is also reluctant to call his mother; we live in Florida and she lives in Hawaii. She has dementia as well. He says that the conversations are so vague and do not change. I remind him that you don't call to get new information, but to remind her that you love her. I also send her monthly letters and try to send pictures and occasional "fun" things now that she is essentially a shut-in with COVID-19.
Very well put--sometimes just hearing the other person's voice is a treasured gift. I recall an advertisement along these lines (I believe from the phone company in Spain, back in 1988) that went "the best gift is the sound of your voice".
there are other things that get people down such as CoVID-19, bills, possible unemployment, and this yet another stress. Alzheimer's only gets worse until they die. My mom had it for 15 years, and it destroyed her life and mine. She died 6 months ago and I have not recovered and probably never will. What can you do? Just go on living. Or crack up. I slowly watched my mother die as she declined and it took years and years. The last years of her life she even depended on me for her bowel movements. Feeding tubes...and if she did not poop in 3 days she would get so severely impacted. Try living with that for years, and see what it does to you.
Slowly dying of a chronic disease like Alzheimer's never prepares you. Yes I lost her years ago even before she died but she had her rare moments she came back for a short time. Very rare moments. When mom died I miss her so bad I would gladly give my soul to the devil to have her back. But that would not be fair to her even if it were possible.
People die. Always have, always will. One day I will die. As odd as that sounds it is strange comfort and suddenly you have this sense of peace..I did all I could for her. Nobody on earth would have done better. Mom died in absolute peace and without drugs. Perhaps all this bitterness and sadness is replaced with this peace--her death was a natural thing. She was 90. I was blessed to have her that long. Very blessed.
I can't say mom's years were bad. Mom did not suffer and she was very comfortable. She felt loved and secure in her home and routines.
cetude, you've obviously done a wonderful job caring for your mother whom you loved so much, and you've described it wonderfully but realistically here, too!
Men are different. I know, because I am one.Honestly,the best help you can give him is space. Men get a bad rep. because we "don't want to deal with feelings". It's really not like that at all. We come in a lot of different verities, but one thing we all have in common is armor. You can't hug and squeeze your way in. He is processing his feelings. The better his relationship was with his mom, the harder this will be for him. I know you want to get inside his head and be a good wife. That is, after all, what a good wife does. :) Just be there for him like a safety net. He'll come to grips in someway. He's losing his mom one piece at a time and that can be worse than her passing. My grandmother used to say that every boy is more his mother than his father. The lucky ones are anyway. My advice is to stand beside him. He'll let you in when he's ready.
I don’t think the worry is so much about how to handle his Mom as it is about getting Alzheimer’s too. Being a hereditary disease he is probably in fear. You need to talk to him and convince him to get tested or find some other way to accept he my contract it. Start with your doctor. Who knows, he may not carry the gene.
Check out the Alzheimer's Association (alz.org). They have moved many of their educational and group support resources online. I think it might be helpful if you could find a support group for people who have loved ones with Alzheimer's. He could just listen if he wasn't the kind of guy who would participate in group counseling.
It is apparently a very common reaction. But I agree with you that he might feel better in the long run if he shared his feelings- especially with people who really know what he's going through.
Sometimes even just hearing someone else say "I don't want to visit him" just makes any guilt or shame about feeling that way easier to deal with.
If her diagnosis is fairly recent, he should spend time with her while she still knows who he is. It is sad, but right now moments of lucidity are precious, and he can't let his depression waste them. Get him to join this forum too. It helps us.
You mentioned him going to talk to someone about it to help him talk through it but he said no. What if you made an appointment for the two of you to go together. Tell him you need to talk to someone and need him by your side. Then hopefully the therapist will be able to get him to open up too. It would be important for you to allow it, not correct him and to not talk for him.
I get where he is coming from. My moms new diagnosis of Lewy Body Dementia and the huge swings from mildly confused to severely confused is so difficult to witness. It depresses me each time she is severely confused and does not know me..She was admitted to a memory care unit 3 weeks ago. I dread calling her. When she is agitated and barely knows me it is so distressing. The days I call and she is mildly confused are easier. I have hired a Mental health counselor to help me talk this out and it is getting better to tolerate. I try to cling to the days when we can really “connect” and I am learning to find some humor in the confused crazy stories mom tells me. I think counseling would benefit him but as a retired Geriatric clinical healthcare person I wonder if his mom does not know him why can’t he just not visit as often..I believe the visiting in some circumstances is for the family member, to make us feel like good children, not for the parent who does not know us....How does it actually hurt her if she does not know him? Maybe we are judging too harshly? Let the family members who tolerate this well to monitor staff and her care..My brother really is affected badly by this so I chose to be the one who watches over her care..He visits and calls when he feels strong enough to tolerate it.
I was in my twenties when my dad developed alcoholic Alzheimer’s from binge drinking. He usually didn’t recognize me when I visited him in court-ordered Long Term Care and he was often angry if he had no cigarettes. Smoking calmed him down and he enjoyed sitting in the smoking room. To see your parent like that is unbearable but I used to listen to music before I went to visit and do some deep breathing. Sometimes if I sat long enough beside him while he smoked, he would begin to remember stories from his childhood and I learned a lot about our family. When the negative behaviour was exhibited, it left me with jumbled feelings and even pain in the pit of my stomach but then I would visualize him when he was at his best and this really helped. My dad lived over 25 years like this but I never really got over it, just learned to live with reality and accept that the dementia was an illness.
In my mother’s memory care facility of eight residents, only myself and one other family visited their family member on a regular basis. It’s not so unusual to be afraid and sad about Alzheimer’s and dementia.
If your husband cannot bring himself to help out his sister, or even visit or call, could he pitch in with financial help to his sister for taking care of Mom? Is there Something, Anything that he can do?
What happens if, God forbid, in the future you should fall ill or succumb to dementia? Will he just freeze, or leave you? That’s what I would be thinking about in the back of my mind. I would press him to activate and do something. He is probably already damaging his relationship with his sister with the ostrich act.
When my grandmother and I visited my dad in long term care we would plan an outing for ourselves after the visit. My grandmother liked to go to a Chinese food buffet and sometimes we would call and invite friends to eat with us, our treat. Maybe if you approached it that way and he got to go do something he likes after the visit he would be more enthusiastic and he would begin to associate the visit with something pleasant. I know that after my uncle used to visit my dad he used to go and play pool and have a few beers at the Legion which was near the LTCH.
Love0522, it will be a balancing act so that you're not enabling a fully grown man. Tippa Snow is an expert on dementia + ALZ and has many videos available on YouTube. She is lively and entertaining, even on such a difficult topic. Watching some videos together may help him to learn what to expect, and give him words and actions to say + do during his next visit. Maybe agree that on his next visit you do all the talking and he can just be present. But the hope/expectation is for him to eventually visit more and interact with her. I understand that many shut down in emotional stress, but he is an adult. I would gently insist he man-up, grow up and do the right thing. Ask him if that's how he'd treat you if you were in that situation? Would he want to be treated like that by you or his children?
His sister w/new infant should absolutely not be taking on the whole of his mom's caregiving. Maybe sit down as a family and divide up tasks. He can start by doing things that don't involve interacting directly with her -- at first. But if he can't collect himself enough to act maturely then a discussion should be had about transitioning her into a care facility. If this doesn't happen, the sister will burn out and his mom will be in a suboptimal environment. Not acting is an act. There will be consequences no matter if he stays frozen or if he slowly moves forward. Please point this out to him. I would suggest seeing a counselor, but men aren't usually very excited about this, however it may be your ultimatum for him. I wish you success in encouraging him to be brave.
My brothers didn't deal well with my Moms Dementia. Her last year, she declined so much. Looking so frail. One brother lives 7 hrs away. Came for a long weekend. Saw Mom 1x. Just couldn't go to see her 2x.
You might be able to help by learning all you can about Alzheimer's and tell him what you've found out. He might be afraid of the unknown. Leave articles around for him to find and read for himself. Perhaps go visit his mom yourself and report what you've witnessed. Some people just cannot cope with the changes in their parents. My brother won't visit our mother. Only one of my sons visits. If there is a particular chore that needs done at her house, that might be a good excuse to get him there. Some people need practical reasons to do things. Just suggestions. It's wonderful that you want to help him adjust. Good luck.
It sounds as if you’re expecting her to start taking care of MIL as a natural progression with your instructions? The man needs to wake up and take action himself. She shouldn’t be expected to do all this work on her own, while husband gets to hide and play like Prissy, in “Gone with the Wind”. I always wonder how/why women end up taking care of a mother-in-law for years. Now I know.
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.
My husband is also reluctant to call his mother; we live in Florida and she lives in Hawaii. She has dementia as well. He says that the conversations are so vague and do not change. I remind him that you don't call to get new information, but to remind her that you love her. I also send her monthly letters and try to send pictures and occasional "fun" things now that she is essentially a shut-in with COVID-19.
Slowly dying of a chronic disease like Alzheimer's never prepares you. Yes I lost her years ago even before she died but she had her rare moments she came back for a short time. Very rare moments. When mom died I miss her so bad I would gladly give my soul to the devil to have her back. But that would not be fair to her even if it were possible.
People die. Always have, always will. One day I will die. As odd as that sounds it is strange comfort and suddenly you have this sense of peace..I did all I could for her. Nobody on earth would have done better. Mom died in absolute peace and without drugs. Perhaps all this bitterness and sadness is replaced with this peace--her death was a natural thing. She was 90. I was blessed to have her that long. Very blessed.
I can't say mom's years were bad. Mom did not suffer and she was very comfortable. She felt loved and secure in her home and routines.
He'll come to grips in someway. He's losing his mom one piece at a time and that can be worse than her passing. My grandmother used to say that every boy is more his mother than his father. The lucky ones are anyway.
My advice is to stand beside him. He'll let you in when he's ready.
It is apparently a very common reaction. But I agree with you that he might feel better in the long run if he shared his feelings- especially with people who really know what he's going through.
Sometimes even just hearing someone else say "I don't want to visit him" just makes any guilt or shame about feeling that way easier to deal with.
If your husband cannot bring himself to help out his sister, or even visit or call, could he pitch in with financial help to his sister for taking care of Mom? Is there Something, Anything that he can do?
What happens if, God forbid, in the future you should fall ill or succumb to dementia? Will he just freeze, or leave you? That’s what I would be thinking about in the back of my mind. I would press him to activate and do something. He is probably already damaging his relationship with his sister with the ostrich act.
His sister w/new infant should absolutely not be taking on the whole of his mom's caregiving. Maybe sit down as a family and divide up tasks. He can start by doing things that don't involve interacting directly with her -- at first. But if he can't collect himself enough to act maturely then a discussion should be had about transitioning her into a care facility. If this doesn't happen, the sister will burn out and his mom will be in a suboptimal environment. Not acting is an act. There will be consequences no matter if he stays frozen or if he slowly moves forward. Please point this out to him. I would suggest seeing a counselor, but men aren't usually very excited about this, however it may be your ultimatum for him. I wish you success in encouraging him to be brave.
I always wonder how/why women end up taking care of a mother-in-law for years. Now I know.