Hi, I'm new, just found these forums today. I have not been diagnosed as having Fibromyalgia but I suspect it's what I have. Here's a brief overview.
Back in 2007 I started taking zoloft for anxiety, and shortly thereafter I started getting muscle pain, like electricity going through my muscles. I have joint pain too, but it's overshadowed by the intense muscle pain. In about
2009 my sinuses started getting stuffed. Not runny like allergies, but more like swollen so that I can't breath, mostly when I lay down at night. My neck was also starting to hurt at the same time as my muscles.
In Aug 2010 I stopped the zoloft, thinking maybe it was causing the muscle pain. March 2011 I started getting a sore throat, and still have it, and it's getting slowly worse. My neck pain is so bad I finally broke down and started physical therapy to help it. I also grind my teeth at night now, and never used to before. The last couple of months I've also started getting minor, annoying headaches. And I never have been prone to headaches before.
Also over the years I've started loosing my ability to concentrate. Work is getting harder for me all the time. I'm a programmer so I really need my dumb brain. LOL. I also don't sleep very well, and finally got some Ambien from my GP.
I also love to do agility with my dogs, which is very physical and I'm on my feet sometimes 12 hours a day on the weekends. I've gotten to the point where this takes so much out of me physically that it takes a week or more to recover from a weekend of activity. Used to be it only took 2 or 3 days to recover, but this last time it took me a week. UGH. It's my passion and what I love most in the world, so I'll suffer through it, but it does affect my job in a negative way. I get so tired, my muscles are just one fire, and I want to sleep all day afterwards.
So anyway that's a big nutshell.... LOL. But last month I decided I need to start pursuing the doctor route. So I started with a Naturopath, but he didn't really want to diagnose FMS and gave me some Vitamin A and D which hasn't seemed to help much. So I went to my GP. She sent me to a Neurologist who did a Brain Scan MRI which came back normal (she though maybe I had MS). I need to call the Neurologist back. But I figure I need to follow the doctor path, and see what they can find. I'm thinking it's FMS, and perhaps I can find a doctor here in Utah to help me out with it. But the resources in Utah are pretty slim it seems.
Oh... I was also diagnosed as having Interstitial Cystitis in November of 2010. I was really hoping that controlling that would help me in other ways, but it hasn't really. However, I'm glad that I don't feel like I have a bladder infection all the time now, when I really don't. That is miserable. I control it with diet, which works fine!
Cynthia
Post Edited (CynthiaBlue) : 7/18/2011 10:24:23 AM (GMT-6)