She is on bed rest. PT and OT are all that can be done, but she is refusing PT. She is in mid-stages of Alzhimers. My father just died 3 months ago with Parkinsons and COPD. Until now, mom has had mainly short term memory loss. They have been in assisted living, together for the last 2 years. She was in the hospital for 5 days before moving into a rehab center, where she has been for 2 more days. She has refused PT, getting dressed and says she just wants to lie there and die. She screams when they roll her over to bathe her and said she just thinks it's the end. She is in good health otherwise, and taking percoset, as needed for pain. She has gotten up with help a couple of times, but complains loudly about it and wants them to leave her alone. My brother and I have repeatedly given her pep talks about the need to move so she can return to her assisted living room (where she was happy) to no avail. Before, she needed no help with any grooming, etc. and only used a cane when she went out of the building. She is on 2 drugs to slow down Alzhimers progression.
Have you consulted with the surgeon about aggressive PT should be?
I would consider that hospice might be one of the things you consider.
Also, an evaluation for depression.
Hospice is also a good idea if there is no chance of improving. And with just dementia at play, there is no chance for improvement, unfortunately. Also, if there are drugs to "slow the progression" of Alzheimer's, I'm unaware of them. Besides, why would anyone want to prolong an elders battle with such a dreadful disease?
Anti depression meds may help, but mom may be approaching the end of her life now which hospice can assist with. After a certain point, it's impossible for an elder to recover from so many health blows, and so begins the final leg of their earthly journey. Once my father gave up, he passed away 19 days later from an inoperable brain tumor. Hospice kept him comfy in his AL apartment who agreed to keep him until death. Dad made no progress either in rehab, so he was released in pretty short order.
My condolences on the loss of your dad, and watching the wretched progression of AD which I went thru w my own mother.
Just occasionally an injury with this level of acute pain can spell the beginning of the end. There may be medications that can be added that will boost the pain medication itself, and she may need more pain meds for a while, perhaps even a fentanyl patch.
Discuss with MD. This is a case of doing the best you can and hoping that the immobility doesn't create further, and worse problems, because it may. I am truly so sorry. Think of it as an injury in which the tiniest movement of any part of your body results in acute pain in the core. I wish you the best, but I think she needs better pain management.
While it is likely that your mother has untreated pain or a fear of any movement as her mind may tell her she’s falling, I am sharing my story because my mother suddenly stopped moving, without any injury. Incredibly frustrating - her own worst enemy. And that was one year ago.
Pelvic fractures are very painful . People with them tend to not want to move.
Effective pain management , with pain med on board an hour before therapy starts or a Fentanyl patch may help .
However , Depending on how advanced the dementia is she may not be able to do PT successfully .
Like Alva said she may not move ( walk ) , again . Unfortunately this does happen with the elderly with dementia. I’ve seen it with hip and femur fractures as well .
I’ve visited my LOs in rehab, and in one there was a very fine doctor who was head of the place. I learned how forceful he could be in advising patients in similar circumstances as your mom. He raised his voice and told them in no uncertain terms where they’d end up if they didn’t follow the program. He made it sound like a circle of hell. It was his way of motivating, giving them a last chance to respond to treatment.
I don’t think it ever worked because those patients disappeared to long-term nursing across the street.
Sometimes all you can do is give up. Your mom will do what she wants to do, and maybe she knows best. Keeping her alive to experience full-blown dementia may not be such a great idea. I’m very sorry you’re going through this.
Bed-bound + reduced mobility to turn can = pressure sores.
Get all the right OT equipment;
to aid standing, transfering, comfortable chair for sitting, pressure cushion & air mattress to reduce risk of pressure injuries ✔️
Regular visits & encouragement from PT ✔️
Begin the process of adjusting expectations as time goes on.
Acepting the new normal.
(((Hugs)))
with hospice comes the added care. A wheelchair , hospital bed , hoyer lift, care supplies. RN weekly who will manage meds with physician. CNA twice a week
hospice doesn’t mean imminently dying. She would be reevaluated periodically. I read here where their loved one was on hospice for long periods of time…
I don't see AL as being appropriate anymore, do you?
otherwise just keep loving and encouraging her through the protests. And listen to her. She may need a time to vent her grief still. Find an old friend of hers to call her or visit her. Help her reconnect. God bless you
as with most things in life you can not force someone to do something they do not want to do.
I'd understand mild stage to mean that she is frightened, confused, depressed, responding to medication(s), frustrated, in pain ... and possibly having thoughts of 'you are out to get me.' She will resist as she believes she is protecting herself. And, she may be 'fed up' and just giving up.
The best, if not the only way, to support her well-being is to learn how to communicate with her - and then she has the final word:
1. Talk calmly to her (in an even quiet tone - no screaming).
2. Smile while making eye contact.
3. Reflect what she says back to her (let her know you are listening to her).
4. Provide gentle touch if it is well received (neck massage, shoulder massage, touch her hair while looking into her eyes).
5. She wants to FEEL cared for and she will 'get' these kind loving gestures.
- As you build up trust through these communication ways, she may start to let PT to happen ... although so much also depends on how the PT works with her. That person needs to take their time with her as you will / do. And, realistically, their time is limited. Do all you can to 'prepare' you mom for PT. Do the above (massage, focused attention, and let her know the PT is coming in xxx 1/2 hour so she will know. If she is able to understand, tell her: "xxx, the PT is coming over and it is entirely up to you if you want to work with her / him." Giving her the power to make these choices, even though she already has this power, may help her feel more in control of her life and the decisions she makes = she will feel better and possibly not be 'so' resistant.
Still. Nothing may work to meet this (PT) objective.
One of the hardest realizations to learn is that we / loved ones / family / paid caregiver / manager (me) / medical professionals want to do and try to do, we can only 'do' some much and then we need to let go, accept a person where they are and go from there.
Frustration, overwhelm, depression, dealing with loss of independence, and change, physical PAI, support systems and prior/lifelong patterns of behavior all affect how a person will decide to move in their life - then there is the addition of dementia (which changes / colors everything else.
The best you might be able to do is accept where she is and what she wants, understanding and empathizing with her discomfort and pain.
It is important to remember that it is the brain that is changing. The person cannot make logical / healthy life decisions as they once could/did.
When she says no, try to give her a gentle massage to relax her. That might be all you can do in the moment - and she will appreciate the care and comfort it brings.
Gena / Touch Matters