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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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Mostly Independent
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When my mother-in-law asks why she has such a terrible memory, I just tell her that she still has all the information in her brain, but she can't access it anymore. No sense telling her she has the beginning of alzheimer's she wouldn't remember that anyway.
My sisters and I didn't tell our mom that she had dementia - for some of the time we weren't even sure ourselves!! When she forgot something and said she was getting so forgetful we just said that anyone past 95 years of age probably couldn't remember everything. Mom was not the type of person who liked to admit that anything was going wrong - she kept her diabetes a secret from even her closest friends for years. Because Mom had always been so clever, she would have been SO disappointed to learn that in the end, her brain was failing her. She didn't ask what was wrong and we didn't think anything would be gained by telling her. But, as others have written, not everyone is the same so I would say " Just do what you believe is the most LOVING thing to do for your mom " and don't get uptight yourself about your mom having dementia. You will need all your energy just to "go with the flow".
Hey there Lrock, Everybody's dementia is different. What works for one may not work for another. I told my mom she had dementia because she was a no bs type of lady and so I said do you want the truth or do you want me to just act like nothing is wrong? And she chose the truth so I told her as gently and directly as I could. It worked for my mom because she knew something was wrong and it was a relief for her to finally have an answer as opposed to thinking she was crazy. I told her that I would keep her safe and sound and that she didn't have to worry or be scared. As she progressed through the disease and would experience the different symptoms that are disturbing or frightening, I would say: Aw mom, don't worry, that's just the dementia talking. don't pay it any mind. It was an obvious comfort to her and I told her every day that I thought she was the bravest person I'd ever met because she faced this terrible disease with grace and as much humor as she could muster. My mom had the kind of dementia where she had long lucid moments and then she would fade away for awhile. It was the saddest thing I have ever witnessed and of course it was so sad for mom. Like I said, everyone's dementia is different and the truth worked for her but might not work for you and your situation. Could you tell us more about your parent and what symptoms they are presenting? If you are comfortable with that... one way or the other we all understand. Please keep coming back to this site for the support you will need because you will find the most loving and caring people here like the ones above who have answered your question.
I think most people know when they have dementia-it must be very hard for them to realize that it is happening to them-the best thing you can do is to take them to their primary MD so they can get on meds as early as possible and you yourself learn as much as you can about and if possible join a neuro support group and this site is very important there are many threads here where you can join discussions so you are not alone and get support and assistance from others and where you can vent as needed so you do not feel alone because this disease will affect you greatly often even more than the person with dementia-I remember a doctor increased a med I was on even though I said the dose I was on made me spacy and after taking the stronger dose I got lost going home from church twice and let me tell you it was scary for me.
We have "reminded" grandma often that she has memory problems but she forgets. I don't mean that to be funny.
At the beginning of her dementia, we tried to explain it and her doctor tried to explain it, but in the end it really doesn't matter. If she understood it in the beginning, that understanding is now also lost.
We don't bring it up anymore. Sharing this with her causes her to react with either sadness or anger and we'd rather avoid both. So we operate as well as we can with repeating ourselves constantly, leaving notes on white boards about where we are in the house, and trying to remain sane ourselves.
Hi Lrock, When my Mother asks questions about being confused or not remembering something fairly recent, and she gets upset about it, sometimes I will say, "That's the dementia, Mother." Last time, however, she freaked out and put her hands over her ears and cried, "Ooooh, don't tell me there's something WRONG with me"! I felt terrible that I had said it. After that, I don't think I will tell her again. It's gets a bit redundant and really, it seems kind of cruel to tell them since they are already confused. I had read on another thread that this person used to tell her Mom that she had dementia, and she had a lot more experience than I at the time, so I thought it was OK. Now, I don't think so. Even if they don't or can't respond, how do we know where that comment is going in their brain? Better left unsaid. Only WE need to know they have dementia. They will forget! As their reality changes, our treatment of their behavior has to change, too. Our perceptions are the same, but we are watching a constantly changing picture, and must adapt accordingly. Good luck. You will get lots of answers. Weigh them all for validity, follow your instinct, and you will be fine. Hugs, Christina
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.
Everybody's dementia is different. What works for one may not work for another. I told my mom she had dementia because she was a no bs type of lady and so I said do you want the truth or do you want me to just act like nothing is wrong? And she chose the truth so I told her as gently and directly as I could.
It worked for my mom because she knew something was wrong and it was a relief for her to finally have an answer as opposed to thinking she was crazy. I told her that I would keep her safe and sound and that she didn't have to worry or be scared.
As she progressed through the disease and would experience the different symptoms that are disturbing or frightening, I would say: Aw mom, don't worry, that's just the dementia talking. don't pay it any mind. It was an obvious comfort to her and I told her every day that I thought she was the bravest person I'd ever met because she faced this terrible disease with grace and as much humor as she could muster.
My mom had the kind of dementia where she had long lucid moments and then she would fade away for awhile. It was the saddest thing I have ever witnessed and of course it was so sad for mom.
Like I said, everyone's dementia is different and the truth worked for her but might not work for you and your situation.
Could you tell us more about your parent and what symptoms they are presenting? If you are comfortable with that... one way or the other we all understand.
Please keep coming back to this site for the support you will need because you will find the most loving and caring people here like the ones above who have answered your question.
At the beginning of her dementia, we tried to explain it and her doctor tried to explain it, but in the end it really doesn't matter. If she understood it in the beginning, that understanding is now also lost.
We don't bring it up anymore. Sharing this with her causes her to react with either sadness or anger and we'd rather avoid both. So we operate as well as we can with repeating ourselves constantly, leaving notes on white boards about where we are in the house, and trying to remain sane ourselves.
Hope it helps. Goodluck and hugs.
HB
When my Mother asks questions about being confused or not remembering something fairly recent, and she gets upset about it, sometimes I will say, "That's the dementia, Mother." Last time, however, she freaked out and put her hands over her ears and cried, "Ooooh, don't tell me there's something WRONG with me"!
I felt terrible that I had said it. After that, I don't think I will tell her again. It's gets a bit redundant and really, it seems kind of cruel to tell them since they are already confused.
I had read on another thread that this person used to tell her Mom that she had dementia, and she had a lot more experience than I at the time, so I thought it was OK. Now, I don't think so. Even if they don't or can't respond, how do we know where that comment is going in their brain? Better left unsaid. Only WE need to know they have dementia. They will forget!
As their reality changes, our treatment of their behavior has to change, too. Our perceptions are the same, but we are watching a constantly changing picture, and must adapt accordingly. Good luck. You will get lots of answers. Weigh them all for validity, follow your instinct, and you will be fine. Hugs, Christina