Ok so I will say first thing, I have Medical Power of Attorney for my Mom, and she lives with me and I am her caregiver. She was diagnosed with Lewy Body Dementia, Parkinson's Disease, and has had 3 strokes. She requires assistance with all daily activities, is seriously impaired. We have had multiple falls, and they are increasing. She has reached a point where I am not enough to keep her safe, and my own health is now suffering as well. I need to get her into long term care as soon as possible, and even have a facility picked out and luckily have a niece by marriage that is in social services at the facility. The problem is my siblings and I want to get our ducks in a row before talking to Mom. We do not want to cause undue stress and fear for an extended period of time. She is easily upset and agitated and it sends her into a decline. I tried to get an appointment either in person or phone to speak to her doctor alone and tell her all of her many symptoms I am now dealing with and to get an order hopefully for the facility. The doctor had her nurse call and refuse me and said without guardianship not just medical power of attorney she can't lawfully see me or talk to me alone. I thought that medical power of attorney was for those very things, that the person with medical POA had say over medical treatment and could talk to the doctors? She told the nurse to tell me if I am thinking of long term care to contact social services at whichever facility I want. So my niece at the facility faxed info to the doctor telling her of Mom's condition of decline and our concerns, asking doctor what is needed and requesting a medical order, medications list, etc, etc. That was last week still no word to me or the facility as of yet. Afraid the doctor is going to refuse that too. I feel like I am hitting a brick wall. Hate to call the doctor's office, I felt like I was being talked down to with this disapproving tone that I am doing this without Mom present. I am just trying to get things moving without stressing her too bad. She is very emotional and I do not want to set off a really bad decline, or her to have terrible emotional fits that upsets the entire household for days or weeks with nothing definitive set in motion.
We have had POAs in place a long long time. Despite that, EC atty told us we couldn't force mom to move - she was adamant that she wouldn't move, esp not to AL and that she was fine, independent and could cook. She wasn't and couldn't. POAs allow you to step in for someone else, to sign documents, make financial and/or medical decisions according to the person's wishes. Unfortunately they are not enough to force a move, per our EC atty. He said we would need to get guardianship, but the place we chose wouldn't accept committals, so guardianship would be time consuming, expensive and useless to us!
We moved forward with plans anyway. Made deposit and arrangements for when the MC unit was up and running (rebuilt facility, MC was the last unit to open in IL/AL/MC.) I left it to my brothers to do the actual move (I did MOST of everything else, and wanted to keep the blame off me if possible!), but they really didn't have a plan. I made suggestions, but was ignored. Days before the planned move, she injured her leg and developed a serious infection. It delayed the move a few days, so YB used the time and incident to draft a phony letter from 'Elder Services' at the hospital, which stated she either moves to a place we choose, or they would place her. She was mad as all hell, but she went with them.
We had NO doctor Dx, NO doctor letter, nothing. Facility staff had seen her and knew her condition (YB kept insisting AL, but they said no, MC, so they could tell.) They said to just get her there, they would take it from there, which is what we did.
So, in your case, if you think she needs a NH (doesn't sound like she needs specialized nursing care yet), either push back harder with the doc, or try the neurologist. If MC would be enough, check with the place you have chosen. Do they really need doctor orders? If not, YOU sign everything as DPOA and find a way to get her there (going out to lunch, visiting someone, etc, any fib that would get her to go with you.
Another option is to get an outside assessment. When we tried hiring aides to keep mom in her condo longer, they sent a nurse who did a FULL test in mom's condo with YB and me present. Medicare covers the cost for this. She even came a few more times, due to UTI during this "transition" and her services were covered by Medicare. We did NOT use the results of this test to make the move.
Obviously it is hard on everyone to make this move. You feel guilty for "giving up." They might be angry for a while if you make them move. Honestly, I don't think ANYONE with dementia is going to ever agree that it's time to move. We have to make that decision and somehow make it happen. Sometimes everyone involved works as a team and it can go fairly smoothly. Other times you have docs like your mother's, who just don't get it!
BTW, mom's doc at the time promised a letter I needed to become rep for her federal pension. Federal entities do NOT accept POAs (SS, Medicare, VA, IRS, etc.) They all have their own forms and process. NINE months later, despite MANY phone calls and portal postings, giving them copies of what was needed and why, plus multiple POA copies, some before the appt, some after, I still had no letter. Office staff was the problem. The move was going to require a change in docs, so I made arrangements with the new doctor and eventually (took almost 2 years and 2 letters!) I was able to be approved! SS rep payee was a snap in comparison!
So, you aren't alone when it comes to doctors not being helpful or receptive. If you can, find a way around her.
Thats probably why the doctor isn’t talking .. you don’t have POA .
Good Luck
Some of these dr's are scared they are going to assist in putting someone away against their will and get sued. It's ridiculous...if he knows your mothers medical condition, then he knows she can't be managed by someone at home.
There are some great facilities out there. Do your due diligence and check several out and find the perfect fit for mom.
Take care.
Your physician is your MIL’s doctor, not yours. POA gives you the ability to make decisions if they cannot. Maybe call the doctor’s office and ask for evaluations to get the documentation you need.
We did go to an elder care attorney to find out what we needed to do. It is different in every state. He helped us through the process. The bill was paid through my Dad’s account so we did not have to pay.
I don’t think anything prepared us for how difficult it is when the parent doesn’t understand what is happening. My Dad is still mad at us, but he is where he needs to be. None of us could handle him.
I am now I n the process of finding a Memory Care place for Mom and have talked to 6 facilities this week, none has mentioned needing a dr's order for placement. Each wants to do an assessment of Mom's metal and physical status to determine the best placement for her. They will talk to the current staff and/or doctor as needed, and interview Mom.
I suggest talking with the facility director to find out what they need to place your parent. Also your state's Department on Aging. That doctor sounds like a jerk!
This document consists of the person's level of care needed and diagnosis. We don't decide what level of care our loved one needs. js
Dad's internist never hesitated to discuss realistically what was going on. Via office visits or message center for the clinic. Dad decided, after two of his kids spent about 6 months taking care of him in home, that he and mom should go to Assisted Living. By then, he was also on Medicare hospice status due to multiple hospitalizations for his heart condition. So in AL, he was seen by AL staff and hospice staff. Mom, who has dementia and no short term memory ability, lived there with him without any services until he passed away. After that, mom was immediately moved to the memory care wing since she was unable to manage any of the ADLs without lots of help and prompting (prior to his death, Dad did the prompting.) The PCP was not involved in the placements at all, unless the staff at AL contacted him for some context or to renew an Rx.
Don't understand why her PCP is being so obtuse. If she is at Medicare hospice status (sounds like it,) once the MD certifies her for hospice services (all paid,) either in home or in a facility. The hospice staff takes care of getting her medications and coordinating her care.
If it’s ok from just a needs assessment, usually those are Geriatric RN & SW duo who do a detailed evaluation & score on mom in her home. Some facilities have an in house team that does these. When I moved my mom from NH#1 to eons better NH#2, they sent out a team to visit with mom all bedside. The RN called me as they were there to say all ok as the new place could do the level of care mom needed and then turned the phone over to my mom to chat a bit with me. Pretty awesome. We didn’t pay for their assessment visit, it was done as a part of the admissions transfer process. I imagine it was billed to Medicare or Medicaid in some way.
If your mom tends to “show dog” around strangers, let the assessment team know this in advance. They might bring something new with them to see how mom handles it..... like a notebook with an elastic closure or vitamin jar (she has to open these) or hold a coffee cup that she’s not used to. Y’all have to stay out of the room / house when the assessment is done too.
Now if it’s that she must have MD orders for skilled nursing care, I’d forget dealing with her old MD. Other than her office sending over your moms old medical records to the new NH, I’d find a new MD.
The place where your niece works at, I bet they have a MD who is the part time medical director. And I bet they also still have a private practice. So mom becomes a patient of this MD. Hopefully moms health insurance and whatever ones the new one takes dovetail! He writes the orders for skilled nursing care needed. The plus in going this route as he’s affiliated with a NH, he knows what type of ICD codes need to be in moms chart to define just how she’s needing skilled care in a facility. This will be mucho importante should she need Medicaid later on.
Please Keep in mind that the vast majority- like 70+% - of NH admissions come from a post hospitalization event and they get discharged from the hospital to the NH for rehab. They are a rehab patient at the NH. All this is a covered MediCARE benefit. And they have a fat health care chart filled with ICD codes that show skilled rehab care needed. Most of the articles and experiences are hospital 2 rehab 2 staying & becoming a long term care resident in a NH.
But your mom is still living at home with you. There’s not a fat hospital chart for her. Plus she has a beyond unhelpful MD. She’s coming in directly from home 2 as a LTC resident (not a rehab patient).
If she’s private pay definitely forever for her stay, no worries. But if she’s going to need LTC Medicaid in the near future, you do need to be sensitive to her chart documenting absolute need for skilled nursing care. I moved my mom from IL to a NH totally bypassing the AL phase. It took abt 5 months of MD visits every 2-4 weeks to build up her chart. Unfortunately if they are in IL or living at home there flat is not a fat health chart with notes and frequent lab work that gets stuff enter into often to document need. I had no idea just how beyond unusual it was to do this (IL 2 NH) and do it in relatively quick period of time.
Best of luck!
My guess is you will either have to have your mother get admitted to the hospital for 3 days prior to placement, likely through the ER. This will be distressing to all involved, but might be the only option.
Or take her to the doctor so he/she can do their own assessment about her ability to make decisions for herself. If they find that she cannot, they might be more willing to work with you.
Sometimes, all a "guardian" is … just something on a paper. They are not always for "someone's best interest."
I have medical POA for my mom and once in awhile have received push back or just no response from staff where she resides. For example, I had some time ago requested copies of medical documents so as to update my mom's medical information that I and sibs have available if needed, and then having no response from medical records staff, even after submitting a properly completed request for release of information and that they already have a copy of the legal document for medical POA.
Anyway, keep on with doing what's best for your mom, know your authority, and keep a copy of the legal document (medical POA) on hand and ready to produce.
Hope that helps. I am so sorry for what your mom is experiencing; it is good she has you and others advocating for her. Take care!
You do not need a doctors order to place her in Assisted Living or Memory Care.
You can fill out a Medical Release Form and they HAVE to send the information requested to the facility or to the doctor that requested the information.
She will probably have to get a TB test either skin test, blood test or X-Ray prior to being accepted as a resident but the facility can give you the forms and you can go to any lab and have them done, you do not need your doctor to order them or do them.
The next thing I would do in any case is change doctors.
Just be aware that a move will set off a decline and that is to be expected. How much of a decline is difficult to say. The fact that you have family member that works there might help but I am not sure how much contact she would have with your mom. But it is another set of eyes that will be there for her.
Not all facilities have their own medical staff (mom's does NOT), so that may not be true, but if my mother's doc was being that stupid, she would STILL lose the patient!
We had to change docs because NINE months after telling me I would get the letter needed for being mom's rep on a federal pension (not for lack of trying and sending what they wanted before and after, so they have multiple copies of what was needed), I had nothing in hand. We also would have had to change docs because the facility (MC) we chose was too far away to continue with that office.
After butting heads several times with this new doc (initially all was good!), I had to make a change as she wasn't listening to me and/or denying what mom needed or ordering massive amts of ibuprofen and tylenol instead of getting tests done to figure out where the pain in her leg was. I already had appt set up with new doc, but received a letter from that doc we were ditching announcing her retirement, which came just DAYS before she retired! NO WARNING (and she really wasn't all that old.)
Have you tried to speak with the neurologist?
Is the POA standing or springing needing agreement by two docs of incapacity?
i think you will have to sit her down, explain that her care is too much for you and tell her you have found a lovely facility for her where your niece works. Perhaps you can present it that you need a rest and move is to be temporary. Yes that is a lie but a small one to keep her from imploding. You can then take her to doctor, be present for discussion. Get her to sign HIPAA form so they will talk to you and arrange for a copy of her medical records.
Unfortunately changing docs would require the doc see and examine the woman and see all the tests/records.
In my experience, doctors don't give a darn about the elder's living situation, especially when it's a family member (usually a daughter) who is bringing them to all of the visits. Their patient is the elder. And you've been carting her around to medical visits 2 - 3x/week?
Caregivers need to start being much more forceful about their own health, and to tell their own doctors how caregiving is ruining their mental and physical health. If there had been the serious suggestion/plea from anyone (including my 3 out of state brothers) that our mother needed to move in with me (the local one), I would have consulted with my own doctor and then told my brothers clearly and forcefully that my doctor said absolutely not.
Why on earth do you berate yourself because you want placement for her? I don't understand this guilt that so many have. Do your siblings have any guilt? Shouldn't THEY have guilt, also, if you do? Why don't they have MORE guilt? Over and over again on this site I read of 24/7/365 caregivers feeling so horrible that they can't be slaves any longer. And usually there are siblings who have never done any of it.
Please realize that I am not referring just to you -- I see this over and over again on this site.
Please do what the wise posters on this site have advised. Also realize and expect that once in the facility, your mother will probably get very ugly towards you.