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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.
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.
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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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That can be a challenge, especially since Lewy Body fluctuates so dramatically. If you go along for three days with him behaving "normally" and on the fourth day he does something foolish, it is natural to want to react as you would have when he was "normal." I found it easier to be patient when he had many bad days in a row. Then it is hard to forget that he is impaired.
I found it helped to learn all I could about the disease. Reading and seeing pictures of what the damage looks like in the brain was useful. My mantra became, "This is not my dear husband. It is the damage in his brain."
We called the disease Lewy. More than once I apologized, "Oh honey, I'm so sorry I hollered at you. I'm really not mad at you at all. I'm mad at that darn Lewy."
I went on the Lewy journey with my husband for ten years. I know that it is considered to have one of the highest caregiver burdens, because there can be many behavioral symptoms and they tend to come on very early in the disease.
It really, really helps a lot if his doctors are very knowledgeable about the disease and can explain things to you.
I agree that I would read a lot about end of life decisions. Does your husband have a Healthcare Directive? Did he want tube feeding? I'd try to reconcile how this refusal to eat may be part of his illness and the tube feeding is not without risks and may not increase his longevity. I'd try to honor his wishes.
I also would try not to put unrealistic demands on yourself. This is perhaps one of the most challenging things to handle in a person's life. Caring for someone with his condition in the home is a HUGE responsibility. The behavior of a dementia patient can be exasperating. Who wouldn't struggle with this? Maybe, you are expecting too much from yourself. Maybe, with help, you could have time to restore your resources and recharge your batteries. Then, you can devote more quality time with husband later on. I'd explore getting help. I'm not sure how much you have, but, 24/7 duties will wreck your mental and physical health.
I would imagine that it's very sad to realize that you may not be able to make a dementia patient happy, content or stable. It may be something that is just not within your ability to do. It's not your fault.
You sound like a wonderful and loving wife. I wish the best for the both of you.
A dear friend posted this on his Facebook page the other day, and it was a reminder for me: A person with dementia is not giving you a hard time, they are having a hard time.
Sometimes I need to remind myself of that, as I get caught up in some endless loop argument with my mother.
Thank you, i am in the beginning of this journey and dont really know what i am in for. We have been fighting for a year about not eating, after much weight loss we had a feeding tube inserted for nutrition. I felt like i was just watching him die. Now he doesnt want to even drink ensure. He wants us to do it all by tube even though there is no physical reason for him to not eat. We do have a good day then a few bad days where he just wont do anything. I need to find a place for information, i feel like i am alone in this.
When it's hard not to lose your temper, imagine that the situation is reversed and that it's you who has the LBD. Putting yourself in his place can be traumatic, but it can also be enlightening, and help deal with the frustration.
I learned many things dealing with my husbands Alzheimer's. One that I learned early on, and the most difficult to follow through with is...You can not argue with someone with dementia, you will never win. If he can respond have you, during a calm time sat and discussed this with him? Have you explained to him why it is important to you that he keep his strength up? Have you allowed him to express his feelings as to why he does not want to eat? If he tells you it is because he does not want to live you need to validate that and understand what it must be like for him. And at some point he may ask for the feeding tube to be removed, this is also understandable and as it gets towards the end of his life he will not need food or drink. To keep giving him food and drink it can create more problems. Obstructions, vomiting, and in some cases the food will sit in the stomach undigested. If you have not had an "end of life" discussion with your husband and his doctors it might be time. If he has then you are a step ahead of many. At some point you might want to contact a Hospice to determine if he qualifies. You will have a great resource to help you and your husband with some very tough decisions.
All these comments have helped me as I deal with my husband's new diagnosis of Mild Cognitive Impairment. He's just not the same guy anymore, and I have difficulty remembering that. Thanks, everyone.
For some time now I have come to believe that Dementia is one of a few diseases that remains a dirty little secret. In recent years society has become better educated and therefore more understanding of diseases such as AIDS, Hepatitis C, Psoriasis and even Herpes. But not Dementia. There's a line in the movie Still Alice - about a woman with early onset Alzheimer's- where she says "I wish I had cancer" siting the existing social stigma she deals with from having Alzheimer's. Robin Williams had Lewy Bodies. Famed DJ Casey Kasem had Lewy Bodies. But I'm betting not too many people- even here on this site - are aware of that. So - my point as I stand on my soap box? Help will only become available on a larger scale when Dementia comes out of the shadows. Given our aging population, why are there so few Geriatric Psychiatrists? Why is Medicaid mostly restricted to Nursing Homes and not more Assisted Living and Independent Living Communties? But until people wake up to the fact Dementia is an Equal Opportunity Employer, what can you do? Research, make phone calls, internet searches - ask questions and do not be shy about asking for help from agencies and associations dedicated to the aged, disabled, dementia etc. If you have close friends and family - help them learn and tell them how to be helpful to you and your husband. And if all else fails - you still have the caring, generous people here on this site who will do their best to help. You are not alone.
My dad has dementia (doctors have varying opinions on what type). My mother is verbally just horribly cruel to him. She forbids him to watch TV, so he sits in silence all day. Anything he says, she pounces on him. I have seen the worst behavior from her. It's the opposite of what you should do. Please be patient and speak kindly. Close your eyes and take a deep breath, think about the things you say before you respond. Don't speak to him like he's stupid. My mother loves to loudly declare "he's an INCOMPETENT!!" in his presence. Please let him do small tasks and if they are not done perfectly, move on. If you are lucky enough to get some home health care, be grateful and take full advantage of it. We lined up home health for my dad and mom told them they were an intrusion into her home and she ran them off. Basically, what my mother is doing, do the opposite. When my dad is gone, my mother will likely have 2 decades to mull over her horrible behavior. She is 74 and her own mother lived to 96. Think about how you will reflect on your behavior in the future.
A Caregiver's Guide to Lewy Body Dementia by Helen Buell Whitworth is an excellent resource. My mother cares for my father at home. He is still able-bodied and continent. The most difficult symptoms are his delusions. I know you are supposed to agree with dementia patients but my father's delusions involve all the male neighbors raping their children or other neighbors. He is also a member of the secret police (shh, don't tell anyone) and he kills nuns by falling on them. I try the redirecting techniques but the talk of the neighbors is pretty constant. Sometimes he goes out (we are lucky if he puts clothes on) to save a neighbor. This usually occurs when my mother is in the basement doing laundry. Other delusions are that my mother is out banging her (insert racial epithets here) and that she is going to send him up the river so she can la-di-da with her boyfriends. He's tried hiding the car keys so she can't go out. I live in another state and visit frequently to spell her. Luckily they have very kind neighbors and a lovely retired nurse who comes eight hours a week to give my mother a break because let me tell you it's exhausting. Just keeping him fed, he wants five meals a day with meat and ice cream. And yet, at 6'3" he's only 145 lbs. This was not helpful was it? I guess I am trying to say that I understand it's not always easy to keep your temper.
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.
I found it helped to learn all I could about the disease. Reading and seeing pictures of what the damage looks like in the brain was useful. My mantra became, "This is not my dear husband. It is the damage in his brain."
We called the disease Lewy. More than once I apologized, "Oh honey, I'm so sorry I hollered at you. I'm really not mad at you at all. I'm mad at that darn Lewy."
I went on the Lewy journey with my husband for ten years. I know that it is considered to have one of the highest caregiver burdens, because there can be many behavioral symptoms and they tend to come on very early in the disease.
It really, really helps a lot if his doctors are very knowledgeable about the disease and can explain things to you.
I agree that I would read a lot about end of life decisions. Does your husband have a Healthcare Directive? Did he want tube feeding? I'd try to reconcile how this refusal to eat may be part of his illness and the tube feeding is not without risks and may not increase his longevity. I'd try to honor his wishes.
I also would try not to put unrealistic demands on yourself. This is perhaps one of the most challenging things to handle in a person's life. Caring for someone with his condition in the home is a HUGE responsibility. The behavior of a dementia patient can be exasperating. Who wouldn't struggle with this? Maybe, you are expecting too much from yourself. Maybe, with help, you could have time to restore your resources and recharge your batteries. Then, you can devote more quality time with husband later on. I'd explore getting help. I'm not sure how much you have, but, 24/7 duties will wreck your mental and physical health.
I would imagine that it's very sad to realize that you may not be able to make a dementia patient happy, content or stable. It may be something that is just not within your ability to do. It's not your fault.
You sound like a wonderful and loving wife. I wish the best for the both of you.
Sometimes I need to remind myself of that, as I get caught up in some endless loop argument with my mother.
I need to find a place for information, i feel like i am alone in this.
If he can respond have you, during a calm time sat and discussed this with him?
Have you explained to him why it is important to you that he keep his strength up?
Have you allowed him to express his feelings as to why he does not want to eat? If he tells you it is because he does not want to live you need to validate that and understand what it must be like for him.
And at some point he may ask for the feeding tube to be removed, this is also understandable and as it gets towards the end of his life he will not need food or drink. To keep giving him food and drink it can create more problems. Obstructions, vomiting, and in some cases the food will sit in the stomach undigested.
If you have not had an "end of life" discussion with your husband and his doctors it might be time. If he has then you are a step ahead of many. At some point you might want to contact a Hospice to determine if he qualifies. You will have a great resource to help you and your husband with some very tough decisions.
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