My mother has severe arthritis in her hip and is no longer able to transfer from bed to wheelchair. Because of advanced dementia she does not qualify for physical therapy. I have to find a new home for her that will support a bedbound resident with advanced memory loss and incontinence. She does not qualify for skilled nursing or rehabilitation, so she will be living in a private pay assisted living residence. Insurance does not cover her situation. Does anyone have experience with this type of situation and what are some of the things I should look for in finding a new home specifically for a bedbound resident and what expectations should I have for her ongoing care?
Do feel free to call facilities in your area, however, because there is a good deal of variety out there.
Here is an informative article from this forum:
https://www.agingcare.com/articles/medicaid-and-long-term-care-133719.htm
When my dad was in skilled nursing, he had a neighbor that was bedridden from a fall that broke her neck, she moved to the AL wing and paid 3k for the room and 4k for the care provided, which was the highest level of care. She was completely bedridden and could not do anything for herself.
I think continuing care facilities offer different services then a free standing AL.
Best of luck finding the best facility for her needs.
Here Memory Care units are often smaller & take folk with various needs - from fully mobile to bedbound. But places vary a lot.
I visited a MC that had a few bedbound residents. Some chose to stay in their rooms but some in 'princess chairs' (recliners on wheels) were moved around & included in activities if they wished / seemed to enjoy it.
My LO spent some respite time in AL with independently mobile folk but was assessed as assist x 1 to get to the dining room & many other tasks, so next stay a higher care section was suggested.
Finding the right 'label' to box people into.. makes me sad 😥. Care should fit around the person ❤️🤗
Bedbound is usually a HUGE factor in where this line is drawn, extensive medical need is another, and severe memory impairment is another. Those may actually be kind of the three big checkboxes. And it seems your mother certainly checks at least two of those boxes for sure and while you only mention severe arthritis, are there other medical needs that would contribute to her need as well?
I'm not so sure I would settle for AL without further investigation. You say skilled nursing facility is not an option - but I'm curious who told you that. And was it a single location or a doctor? She has needs that sound too advanced for an AL at this point.
Have you been able to research the rules and regs for such placements in your area?
If so, have you determined that she “She does not qualify for skilled nursing….” based on information you’ve been given at individual facilities?
In my area, your mother would not qualify for assisted living because of the degree and severity of her physical and cognitive limitations.
Is your mother’s care completely dependent upon HER financial resources ALONE? If you are attempting to “shield” or “shelter” financial resources- a house or other property, or any other assets, you may have to consider some liquidation of assets. In any situation HER assets, NOT YOURS, should be used for her care.
Hoping you are soon seeing progress in your search.
Long term care is the appropriate setting - medical oversight, nurse on duty, and trained aides, in a place with the necessary equipment. Not saying it will be wonderful.
Just a quick Google search - "The BEST candidates for Assisted Living communities are INDEPENDENT individuals who can handle the bulk of their day to day activities without requiring a lot of assistance". Conversely "the best candidate for Skilled Nursing Facilities are those who require constant supervision and care 24/7." (Seniorguidance.org)
While SNF generally do include some medical component - BEDBOUND is also an overarching component.
So, if you are able to find an AL that will take her -you are likely going to have to take the highest level of add-ons AND possibly have a 24/7 private caregiver (or 3 shifts of 8 hours or something along those lines) to ensure that she gets the actual interventions that she needs.
ALs offer help with ADLs, so the incontinence could potentially be addressed. But my concern would be that she isn't going to get constant attention and since she isn't able to transfer herself she will be 100% dependent on their routine or schedule. So it will be truly up to you to find an AL that fits her needs and supplement strongly with additional private aides. Because I would assume that you would need to depend largely on the assistance of private aides to help her more frequently than the AL staff through out the day depending on her needs.
Mom's place had one man in particular who had a raised, reclining wheelchair that looked almost like an ambulance gurney that could be raised at the head and knees. (Kind of like this, but the legs could be straighter than this one -- https://www.spinlife.com/Karman-Healthcare-Lightweight-Tilt-in-Space-VIP-515-Recliner-and-Tilt/spec.cfm?productID=95424&adv=googlepla&utm_medium=CSE&utm_source=googlepla&utm_term=&utm_campaign=610148043&gclid=CjwKCAjwp7eUBhBeEiwAZbHwkecIrZLwUiZXtdPKnv6HNX5lKq9tZgYeyR0XvaF9PTU8YjA4VaUtPRoCiwUQAvD_BwE )
The caregivers had him out in the common room all the time, and I assume they used a Hoyer lift to transfer him from chair to bed.
My mother's MC offered great care options for all residents, but you'd have to speak to the facility administrator directly about what services they provide before you sign on the dotted line. Remember, too, that with advanced dementia at play, there is only SO much stimulation/activity that CAN be offered to your mother in any given day! With the mobility restrictions added in, that would limit her as far as scenic drives on the mini bus too, unless she could be put into a wheelchair and loaded onto the bus that way, which would be another good question for you to pose.
Best of luck!
In many areas Assisted Living and Memory Care facilities are no longer permitted to use "equipment" to transfer a patient / resident.
If a person needs to be transferred using equipment that would be a Long Term Care or Skilled Nursing facility.
I think you should double check I think that you will find that your mom would qualify for Skilled Nursing or Long Term Care. And I would fight that if it is denied.
Is mom on Hospice? If so ask the hospice Nurse and Social Worker to help find placement that would be appropriate.
If she is not on Hospice I would call, get her on Hospice then use the staff to help you find a place that would care for her.
I would be asking the facility how they ensure she is not left to get bedsores and what they do to help her have some stimulation and enrichment.
That all should be made part of her official care plan, no matter where she goes.
Why doesn't she qualify for NH/Memory Care if she is bedbound and can no longer able to transfer? You may need a dr to document that she needs NH for medically necessary assistance. Or are you saying she doesn't qualify for a Medicaid bed in a NH due to her assets and income? You can self pay with her money until she spends it down and if you keep facility aware of her money balances, they are usually good about helping you apply for the Medicaid bed.
I get that there is a reluctance to disrupt the person needing care and move them to a different home, but once bed bound they likely will need to move to a different part of the facility anyway, and in my opinion once your word shrinks to four walls the setting hardly makes any difference. You may be counting on familiar staff, but even that isn't a guarantee because of high turnover, plus many employees of an AL work there rather than at a NH because they don't need to provide that level of care.
How many other patients do they have with similar needs?
How close would her room be to the nursing station?
How much staff do they have for each shift?
Do they have programs such as pet therapy, etc. to keep her occupied/entertained?
I hope this helps.
i don’t see where an AL is capable of providing that level of care. And you will want to be sure there’s enough staff.. post Covid , help is difficult to find… they just don’t pay these people enough !
At my mothers memory care , evening/ nights just two people on. Weekends .. I dreaded..as same .. my mom ended up in diapers, unable to stand to transfer, became two person assist. One day I was there, and she had diarrhea… after 35 minutes no answer , I went and found someone… yes they were busy….but just same …
AL is for where people can assist themselves and the AL fills in the blanks.
I’m not complaining, though. He is well-treated there, and they did not bar me from seeing him during the pandemic, unlike the first place he was in, that gave him Covid (the reason he’s now unable to walk) because they ignored the other resident who was clearly sick and let him infect the entire facility, dropped him last Christmas and tried to blame it on him, stole, etc. You have to be very on top of your loved one’s care at all of these places.