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
[email protected] 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.
*If I am consenting on behalf of someone else, I have the proper authorization to do so. By clicking Get My Results, you agree to our
Privacy Policy. You also consent to receive calls and texts, which may be autodialed, from us and our customer communities. Your consent is not a condition to using our service. Please visit our
Terms of Use. for information about our privacy practices.
Not me. LOL. I guess I need to work out more.
I will try to keep an eye out for more subtle signs. For example last night she told me that it itched. Maybe that is her way of feeling the pain. We are expecting a home wound care nurse today. I will mention it. I hope someone shows up. No one came Sat due to some confusion with her insurance. Luckily the doctor had given me some supplies and I changed the bandage myself. I am now out of zeo form so I hope someone comes. I am waiting for a call back from the agency.
And that's okay with me, her POA for healthcare. Maybe the receptors for pain just aren't functioning as well as before which could account for the lack of feeling pain. I don't really care....she is pain free at a time that, if she were, would just create so many more problems. It is a blessing in my opinion. Altho, I will add that, when she does feel pain from a fall, stitches, or in her head (not headaches), she does mention it, which is good. When Mom does complain about pain, I sit up and take notice because it is so rare that she does.
After reading the comments I suggest she receives the meds for pain. It's very important to keep her comfortable especially since she more than likely can not remember the words to verbalize her discomforts.
I will pray for the both of you.
I hope my reply helps.
DH complains more about everything. :)
But he's still here so I just work with it. :)
“because their brain doesn’t work well enough to put pain and expression together...”
facial expression, voice volume, making sounds during actions, guarding of body parts, grabbing or holding objects, grabbing or holding you, repeating a movement or action over&over, more confusion and disorientation, refusals, anger towards others, crying, whimpering, whining, grunting, gritting teeth, stillness - no movement, holding breath, complaining, begging for help, not eating or drinking, asking for God's help, wanting to "end it all", begging you to "please do not hurt me"
And it is harder for:
- people who can't talk
- people in late stages - not aware of their needs
The above comes from Positive Approach to Care program developed by Teepa Snow. If you are not familiar with it yet, I strongly recommend you search their website and you tube channel.
There can be head pain, bone pain, joint pain, meds pain, wrong shoes, trousers, diapers, hair etc. Thousands of reasons. There can be a spiritual pain as well. They do feel pain - but we are so focused on dementia symptoms, that we do not read the signals, they send to us. We need a new approach to dementia care.
My Husband had a very high pain threshold for as long as I knew him.
My biggest problem was he became pretty much non verbal very early on in his diagnosis so I had to look for facial clues, a grimace or furrowing of his brow to determine pain. But often that did not work either.
I think what happens may be two fold.
The pain is constant so a particular level of pain then becomes "normal" that combined with the brains inability to express in words the pain. And I think since the "wiring in the brain" is short circuiting anyway the misfires may not transmit to the pain receptors.
I think many people with chronic pain become so used to the pain that they would not know what "no pain" would feel like any more.
PLWD can feel pain but they cannot identify, describe nor isolate it. They can say "I am fine", but you can see that their behavior changes. And this change can be extreme - aggression, anxiety, pacing OR they withdraw completely.
There is a huge misunderstanding in the world about feeling pain in dementia. Instead of being given pain killers, they get antipsychotic medication. Because we see aggression as dementia symptom, whereas the reason for aggression is untreated pain.
Watch this video: youtube.com/watch?v=9kSjHtHSJCw
It is an eye opening knowledge.
I also think that many of the very old are so used to experiencing generalized, chronic pain that they just accept it in the same way they accept the other infirmities the now live with. It doesn't mean they couldn't feel better without regularly scheduled pain medication though.
And finally, I know my mom is unable to articulate when and where she has pain, so when she seems "off" it takes some investigating to try to figure out what the problem is. And since she isn't on anything stronger than tylenol the nurses tend to dismiss her pain as minor rather than take it seriously, I think poor mom just survives in a near constant low level of misery.