We appreciate all the help we are getting but it seems she is a totally different person when the doctor or nurse or cna is around. They don’t see how she fights us on everything. Even giving her a bath is a struggle. They are supposed to be getting her in a facility soon but it may take awhile they say because things are just backed up. Our nerves can’t take it anymore. We love her but it’s time for her to be in a facility now. How do we remain sane til this happens?
I would talk to the hospice nurse or PA about what kind of medications that might help with her combative nature when they're not around, I'm sure they can prescribe something that should help calm her, as that is their job.
Hospice also provides volunteers to come out and give you a break, so you may want to ask about that as well.
Hang tight. The hospice social worker will have much better luck in getting your MIL in a facility much quicker than you could on your own, so take some deep breaths and let them do their job.
I wish you the very best.
How is Hospice helping with Medicaid? Make sure you are kept in the loop. In my State you have 90 days to apply, spend down, get Medicaid info required and find a facility. If not done in that time, you start all over.
There is medication that can calm down Mom.
If your MIL does indeed have dementia and you are waiting for her to be placed, you should first educate yourself to her condition so that you can have less combative interactions with her. Teepa Snow videos on YouTube are an excellent help, as are other books (see Discussion section for a recently recommended one which I can't remember the title) and "The 36 Hour Day (can't remember the author).
Please try looking at her with different eyes now: she can't help how she is IF she has dementia.
Can you hire some temporary at home help before she gets placed?