Anonymous wrote:Here is what I had to remind myself. We all know we are going to get old. By middle age many of us have seen many permutations of what aging can look like from grandparents, aunts, uncles, friends' loved ones and we've heard the stories. Then we deal with our own parents. We can choose to bury our heads in the sand and we could end up in dire straits because of it. Or we can plan for ourselves and move to appropriate places in say our 60s. My own parents were conveniently too "busy" to visit their own parents much and all those they had buckets of money they refused to engage in conversations about planning beyond demanding they stay in their own home. They refused to explore what that really looks like. Everyone in their lives went into assisted living/memory care/nursing. You could not explain to them friends will move away, hired help won't always show and we may have to hire a stranger to live with them when they are no longer capable at all. Those conversations ended with screaming fits. Then life happens and there they are with a caregiver they abuse verbally who quits, family setting boundaries, a social worker they yell at and friends have stopped returning their calls. They had decades of retirement to explore things, but were too busy traveling, guilt tripping their kids and shopping to care.
Anonymous wrote:OP obviously your aunt WANTS to be at home, that’s why she is getting hospice care. Or do you think this is about you?
Anonymous wrote:Anonymous wrote:So since my aunt is end stage pancreatic cancer, lives alone ,has no kids, I guess the hospice will leave her in bed to die and rot,right? Because I am leaving in a week regardless - I have no choice.Anonymous wrote:Medicare services are based on medical necessity as ordered by the physician, not on what is easier for the social worker. However even for people who qualify for in home personal care services (people who meet nursing home level of care and meet Medicaid income and eligibility requirements mostly) it is extremely hard to find qualified workers right now. Also extremely hard to find nursing home beds. Social workers can’t fix that.
Do you think the social worker has more choice to move in with her than you do? Or more responsibility?
I'm not saying you have responsibility to do so. I'm saying your problem -- and it is a problem, since you are taking it out on other people -- is in insisting others have more responsibility than you. It is not sufficient to compel you, but that does not follow that that it must then be sufficient to compel them.
Anonymous wrote:So since my aunt is end stage pancreatic cancer, lives alone ,has no kids, I guess the hospice will leave her in bed to die and rot,right? Because I am leaving in a week regardless - I have no choice.Anonymous wrote:Medicare services are based on medical necessity as ordered by the physician, not on what is easier for the social worker. However even for people who qualify for in home personal care services (people who meet nursing home level of care and meet Medicaid income and eligibility requirements mostly) it is extremely hard to find qualified workers right now. Also extremely hard to find nursing home beds. Social workers can’t fix that.
So since my aunt is end stage pancreatic cancer, lives alone ,has no kids, I guess the hospice will leave her in bed to die and rot,right? Because I am leaving in a week regardless - I have no choice.Anonymous wrote:Medicare services are based on medical necessity as ordered by the physician, not on what is easier for the social worker. However even for people who qualify for in home personal care services (people who meet nursing home level of care and meet Medicaid income and eligibility requirements mostly) it is extremely hard to find qualified workers right now. Also extremely hard to find nursing home beds. Social workers can’t fix that.
Anonymous wrote:Sorry social worker. Maybe I’m thinking of a discharge coordinator? They have to figure out a safe discharge plan. I assumed it was easier to do if they could just send them home with a caregiver, rather than needing to set something up.
Anonymous wrote:Anonymous wrote:
All I was looking for was why my aunt was legally entitled to via Medicare. Why be cagey about that? Surely there is a directive?
OP, I'm a caregiver for my husband, and I get where you are coming from.
The entire system is set up to assume and expect that the "loved one" will do everything to take care of the patient. With no training and certainly no compensation from the insurance company.
I learned that there is a diagnostic code that essentially says something like "no caregiver able or willing"
Here it is:
The following code(s) above Z74.2 contain annotation back-references that may be applicable to Z74.2:
Z00-Z99 Factors influencing health status and contact with health services
Z74 Problems related to care provider dependency
Approximate Synonyms
No able caregiver in household
ICD-10-CM Z74.2 is grouped within Diagnostic Related Group(s) (MS-DRG v39.0):
951 Other factors influencing health status
The Social Worker doesn't have anything to do with a diagnosis of course. But I assume her life is made easier if there is an able caregiver. Otherwise she has to do more work to ensure care for the patient.