I didn’t talk about my experience being injected with IV pain meds. They tried a non-naarcotic first and that made me hurt worse. It had a rolling effect where it would hurt less, and then it’d hurt more. When it hurt more, my pulse would race and set off the alarm, which just stressed me out further until I figured out what was going on. Then I’d just watch it.
I couldn’t sit still. I tried lying down, only I kept tossing side to side (they put the railings up, clever people). I tossed the blanket off three times because I was just that uncomfortable. Then I asked for a chair. Then the chair wasn’t comfortable. Then I tried to stand. No good. It was brutal.
The poor guy on my right came in for some heart-related thing and the woman on the other side of him was pregnant and far more vocal about her pain. I felt sad for him listening to both of us.
So the second time, they also gave me narcotics. As my doc said yesterday, “I can’t believe how much heavy narcotics they gave you.” I can. Made me woozy, but didn’t knock me flat. It reduced my pain from about 8-9.5 (depending) down to 7-8.5. Progress.
The Fibromyalgia and Myofasical Problems
One of the complicating factors any time I hurt is this: how much of it is real pain vs. how much of what I’m experiencing is altered pain perception because of fibromyalgia or myofascial pain.
For example, if I reach up and run my fingers through my hair and that hurts, that’s fibromyalgia. If I reach up and run my fingers through my hair and it doesn’t, no fibro. That’s a really clear-cut case.
A myo example: once, Rick reached out to touch my upper arm. It sent shooting pains down my arm and I flinched. That’s myofascial pain. If it had continued after the touching stopped, it could also be partly fibro pain (since I have both).
Bringing this back to the hip issue: given the nature of the hip:
- Some pressure is probably always, or almost always, on muscles that may have myofascial pain issues,
- It’s impossible to tell, at any given time, what percentage of the pain I’m experiencing is fibro-related. Or myo-related.
One thing I do know, though: if I’m sleeping very well, I’m in a lot less pain. I haven’t been sleeping well for a month. Most nights I get a single stretch of 4-6 hours, and that’s pretty much it. I need 8.
The Post-ER Doctor Visit
I had my post-ER doctor visit yesterday.
So my doctor’s like, well, this isn’t really getting better, we need a new approach. I convinced her that probably the best approach was doubling the opioids (tramadol aka Ultram) that work well for my fibro & myo, and halving the opiates (norco) that don’t. Point of clarification here: for me, opiates will mask fibro pain, but they don’t break the flare cycle. But opioids actually break the flare cycle. For me, nothing else has except good sleep (and tricyclics help with that, but haven’t been helping lately).
Right now, I really have zero idea how much of what I’m experiencing is fibro, myo, or neither. It’s probably some evil combination that we just haven’t thrown the right med combination at to get anywhere. (Assuming we don’t have to resort to MRI/CT scan to find some other cause entirely. I’m hoping that’s not the case.)
The opiods also last longer (though not 12 hours, sadly, no matter what the docs say) and maybe I’ll have a chance of sleeping through the night. That didn’t work last night, but we’ll see how it goes.
Catch is, I feel a bit more fragile on the opioids. So I felt well enough to try to cook something. Only that had me shaking and ready to collapse in a heap on the floor.
Two steps forward, one step back. If I can manage enough steps, I think I’l get there.