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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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As with any form of dementia, I think I want concrete answers and sadly they don't exist. Everyone is different, I just hate to see my Dad go through this disease. That's why I wonder if anyone out there is having a similar experience with a father/husband. I read so much about women, but next to nothing about men. You'd be surprised how much doctors don't know about LBD. At first my Dad was diagnosed with Alzheimer's. Not much was matching up with his symptoms until I started looking around at other types of dementia. Also Timothy Hudson , a researcher, has a lot of information on his site. I think my dad's doctor just thinks my dad is old and sees him once a year unless it's an emergency. Specialist are few and far between, over-loaded with patients I'm sure.
A man who is 92 years old now can, on average, expect to live to 96. Of course, you dad is not "average." With no health problems he might die at 93 or live to 100. Both of those would count as part of the average.
He has had LBD 4 years already. If he has the disease the "average" of 8 years, then he can expect to live to 96.
But those are all statistical averages, and I really don't see any way to get a more detailed and specific answer tailored to your dad. His physician is probably the best source of guesses, er estimates.
BTW, is your dad involved in a research program? My husband was. The knowledge of the researcher was excellent!
As far as I can tell, my dad has had LBD since 2014- about 4 years. Yes, my question was with dementia (LBD), could this effect his years left to live since he's already 92. I had a researcher tell me that with LBD, age isn't as much of a factor in longevity as with Alzheimer's disease. Just wondering if anyone had more information from experience of how long this will go on for. At the moment, my Dad can't keep food down, has trouble with balance, has the "masked face" appearance, fidgets, and plays with his tongue a lot. But this will usually pass in a week or so and he'll start to do better for awhile and will keep his food down, thus the LBD rollercoaster. Any experience with this? Thanks-
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.
He has had LBD 4 years already. If he has the disease the "average" of 8 years, then he can expect to live to 96.
But those are all statistical averages, and I really don't see any way to get a more detailed and specific answer tailored to your dad. His physician is probably the best source of guesses, er estimates.
BTW, is your dad involved in a research program? My husband was. The knowledge of the researcher was excellent!
How long has Dad had LBD? Is it moderate? Severe? What are his predominant LBD symptoms?