It's for my mother-in-law who has end stage Parkinsons. She's lost pretty much all control of muscles, is immobile as far as walking, shakes pretty bad, & seems to go in & out of clarity with thinking. She seems to be deteriorating rapidly in the past week.
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We do see people on Forum all the time who claim that hospice hastened the death of their elder, that they didn't understand there would not be further diagnositic testing and etc.
It is important that ALL family involved meet with Hospice and ask any and all questions they can thing of.
I sure do wish you all good luck.
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The alternative for you may be to prolong the end by a few days while MIL is in real pain. I’d suggest that you ask Hospice how long they expect MIL to hang on, and when and what they will do to control pain. The people who object have often left things so late that the end is quicker than they expect, and the shock makes them blame hospice rather than the real killer.
I hope that hospice support will make things easier for both you and your MIL.
The beauty of hospice is that. You'll instantly have a large support network to help you and your MIL through this time of life. They're always there to answer the phone day or night, they nurses come to you, so you don't need to got her in the car for doctor visits, and best of all, the stress just melts away because someone else is sharing the load.
They'll walk you through everything and answer any questions you might have. They have no expectations that you know what's going on or what to do. Call tomorrow and start the process immediately. It'll be a huge burden off you and mom.
Oh, and Medicare pays 100% of hospice costs.