Okay here's the lowdown. I used to have Hodgkin's Lymphoma a year ago. I was treated with chemotherapy. While I was actively being treated for cancer, this woman became my Pain Management doctor. I got healed of cancer and now am in remission.
This lady pain management doctor wasn't giving me any opiates for chronic pain and sent me to another pain management doctor in the hospital who raced me through my visit and gave me shitty Tramadol.
I went up to my (new ) oncologist and complained about how I was treated and sent to some d bag pain doctor.
My doctor agreed that I had a perfectly good pain doctor that I have known for a long time and made me an appointment to see her.
I did my homework, researched my symptoms and came prepared to talk to my origional pain medicine doctor. I wasn't taking any shit. I even called my oncologist and left a message for her to tell this pain medicine doctor(in cancer treatment, they are all on the same team) that I was having long term problems and take my visit seriously.
I finally had visit with original pain doctor. I was polite but direct. I let her know that the medicine I had been given up to that point worked, but was very weak. I am prescribed Vyvanse from another doctor, and I let her know how I felt about Tramadol, SNRI effects and that I wasn't giving up Vyvanse for Tramadol.
Long story short, she asked me what worked, and I told her Percocet (which she had given me in the past). I was then prescribed 120, 5/325 Percocet'. I'll admit I kind of blanked out because I was so happy I was getting my chronic fibromyalgia and misc pain treated with real, working medicine.
After that, she said to let her know on my next visit how the medicine was working.
She then explained to me that the hospital wanted her seeing really damaged cancer patients and not chronic pain patients. I understood, and agreed with her fully to have a new pain management doctor within four months.
Now, I get 20mg of Percocet a day. It definately has a great, noticeable effect. I finally felt like what it was like to be pain free. My tolerance and comfort level is higher than 20mg a day. Honestly 20mg /4 x a day would be perfect. I'm at 5/325 x 4 right now. Now here is where I'm at.
Do I stick with a higher dose IR or get on an ER?
I will present this to my current pain doctor as she is getting me established at the right dosage, so when I leave her, I'm already established and the new doctor will go from there instead of starting me fresh.
Sorry for the long letter/post but this is the entire story. Any suggestions or answers are greatly appreciated.