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Mostly Independent
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My Husband had dementia. Diagnosed with Alzheimer's and I suspect he had Vascular dementia as well. He did not really speak the last 8 years of his life. Different dementias will effect different parts of the brain. In some the loss of the ability to speak is part of the decline as the dementia progresses. He will also probably lose the ability to walk, he will lose the ability for chew and swallow food. Foods will have to be pureed. Liquids will have to be thickened so that he does not aspirate. It is possible that your dad may be eligible for Hospice. Hospice is not just End of Life. As long as there is a documented decline that follows Medicare guidelines a person can remain on Hospice. With Hospice you will get all the Equipment that you need as well as all the personal supplies. A Nurse will come see him once a week, a CNA will come to give him a bath or shower 2 times a week. This is all covered by Medicare or Medicaid. If your dad is a Veteran the VA might help as well. And he may be eligible for more services. And if he is a Veteran if you or Mom are caring for him you can be paid.
This often happens in late stage dementia. And for some it is a primary manifestion of their dementia. Bruce Willis has expressive aphasia.
Do you have any questions for us? I am so very sorry about this condition for your Dad. If you go to the internet you will find that there is a lot of information for you to research under "expressive aphasia and dementia".
Not sure if you had a question, but as I'm sure others have already said being nonverbal is very common as dementia progresses, in particular Alzheimer's.
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.
Different dementias will effect different parts of the brain.
In some the loss of the ability to speak is part of the decline as the dementia progresses.
He will also probably lose the ability to walk, he will lose the ability for chew and swallow food. Foods will have to be pureed. Liquids will have to be thickened so that he does not aspirate.
It is possible that your dad may be eligible for Hospice.
Hospice is not just End of Life. As long as there is a documented decline that follows Medicare guidelines a person can remain on Hospice. With Hospice you will get all the Equipment that you need as well as all the personal supplies. A Nurse will come see him once a week, a CNA will come to give him a bath or shower 2 times a week. This is all covered by Medicare or Medicaid.
If your dad is a Veteran the VA might help as well. And he may be eligible for more services. And if he is a Veteran if you or Mom are caring for him you can be paid.
It maybe time to as about hospice.
Fill us in with more information , I'm sure this is very hard on you and your family.
Thinking of you 😔
Do you have any questions for us? I am so very sorry about this condition for your Dad. If you go to the internet you will find that there is a lot of information for you to research under "expressive aphasia and dementia".
I wish you the best of luck.