My mother has been on Oxycontin now for seven years (I was under the impression it's a temporary fix), or more, to manage pain, she's been seeing a neurologist for.
My major concern is the effects it is having on her health, functionality, and brain workings.
Her RX is now at 20 mg/4x daily. It went to 40mg/4x daily, she made them drop it back. They NOW want to take her to 60mg/4x daily, she refused.
What's going on:
She does not over use it (which happens to be very unfortunate). She has begged her doctor to get her off it because it isn't helping pain and making living for a highly depressed person (before the meds.) more difficult, instead they continually increase the RX.
She attempted to enter a rehab and see other doctors to get her off it and none of them will help, BECAUSE SHE NEVER RUNS OUT EARLY (or, as they explain: "she's not abusing it"), even though she's unable to leave the house, walk properly, remember anything, hold a conversation, ect (her new GP has described her symptoms as in line with a typical stroke victims, w/o the stroke...but is not qualified to make changes ????).
Now, they've found another source of pain, a non-cancerous growth on her spin, which two specialist have not recommended having removed-- but instead decided to increase this prescription AGAIN (the 60mg dosage previously mentioned).
I feel like her quality of life is crashing fast and her, my father, and I can't comprehend any of the rational we receive on why she can't be given better healthcare, when her quality of life is suffering-- they have said there is nothing else to do. She has solid insurance coverage, my father has her covered at work and because she is disabled she has one, or two, supplemental coverages (we've checked they cover a lot).
I need help understanding:
(1) is it normal to observe stroke victim symptoms CONSTANTLY, with this use,
(2) this medical advise she's gotten from several different doctors and/or specialist (DOES IT MAKE SENSE?),
(2) what can we do or suggest?