I think they are leaning towards fibro because I don't have any rashes and the majority of my blood work was normal. The only thing was the ANA and thyroid was mildly elevated but not alarmingly so. It could have been that way for a number of things I suppose.
My ears didn't get better until they gave me steroids, one of the dose packs. Before that I just had meclizine. I was also given steroids and muscle relaxers through IV when I went to the ER and after that my bf said I looked like I had some life back in me. He said I looked sickly before. I was given a prescript
ion for it too.
They originally thought RA but the rheumy said he didn't see signs of that, so he is thinking fibro. All I know is I went from hurting sometimes and being able to ignore it mostly to being in pain everyday all of a sudden. The pain meds take the edge off but it's still lingering in the background and it doesn't take much to aggravate it, like after making dinner right underneath my shoulders and my lower back hurt more and it was one of those quick easy dinners at that. I don't know how long it takes lyrica to help but I haven't noticed a difference so far. I still woke up in pain and just as tired. Of course I've only taken it once so far. I did noticed I felt mentally relaxed though, not much physically.
I also don't have these tender points I read about
, like I've told the doctor, it doesn't hurt to be touched, my body just hurts on its own. Being touched doesn't send me writhing in pain. That's only happened a couple of times and it's been in my calves. The swelling hasn't been super bad, just enough for me to notice. Taking a hot bath or shower only feels better for a moment but doesn't seem like it really has much of an affect.
I don't want to take as much of the meds as he directed because 1) I don't want to be doped up so to say and 2) I'm already sensitive to meds, I always have been. I take my pain meds in halves most of the time and only take 2-2.5 a day instead of 4 as he suggested. I've only seen him once but I'm hoping he doesn't think drugging me up is going to solve everything.
Side-note, I also think they lean towards that because my mother has RA/Fibro. My father however has chronic pain but has never been to a doctor about
it so I have no idea what causes his but it's been that way for most of his life and I know a lot of people in my family, both sides, have arthritis issues, my great-grandmother had some kind of degenerative spine problem. She lost several inches in her height. Either way, whatever is going on sucks majorly and I feel bad for anyone suffering whether it's a minor problem or debilitating!
The majority of the time I've just been pushing through everything because I don't want to let whatever is going on to run my life, but it's gotten to the point that I know there is something wrong with my body for sure and I worry it will only get worse like it has so far. I think I had a flare up of whatever it is, like I was talking about
in my original post, and since then my body hasn't been the same. I really couldn't do anything during that two week period and I worry for when it will happen again because I'm sure it won't be the only time.
One more thing lol, when I was a child I had excruciating knee pain, to the point of being in tears and was diagnosed as having migraines when I was fourteen. Also have had constipation issues for years and recently muscles jerking in my legs. That gets annoying. I'll be sitting still and they will jerk causing the rest of me to move. Not to mention I seem to be dropping things way more than I ever have and forgetting things like crazy, not just the average forgetfulness. I don't know if it's raynaud's or not but my fingers do get extremely pale, including in the nails for a minute when they are cold, they only turned bluish once, although I prefer cold to heat. (Sorry for such the long post)
Post Edited (uniquelythesame) : 6/29/2014 6:16:26 PM (GMT-6)