I haven't been diagnosed yet, but I do have a referral to a rheumatologist. The down side is I can't be seen until February 1.
I am not entirely sure I have fibromyalgia, and maybe I am in denial. It just seems like from what I read, most everyone has it much worse than I do pain wise. I have...
:roll::roll: I recently had a flare up that had my body ballooning. I was told FM doesn't present itself that way but that's beside the point. The point is the "ballooning" is pretty much over, almost nonexistent. I got that shot of steroids about a week ago and thankfully my joints have been...
After weeks indoors i managed the dentist today even though i was scared.
Those of you i have been exchanging with on various threads will know i have been in a bad way for a long time and i just wanted to say i managed the 25 mile (40km) trip and then a further drive out into the countryside...
Hi there.
I just joined today after finally getting a bit peeved about my fibro. I was diagnosed last year, but have pretty much had many symptoms for a long time prior to that, like most sufferers.
I find I can (mostly) manage the everyday pain in my legs since I was prescribed with Gabapentin...
I know the treatment options for FM vary a lot, and am wondering if anyone has found help with either yoga or tai chi?
Even with this most recent flare of fibro, with a painful episode of costochondritis, I am trying to find other treatment options that are more naturopathic.
For me fatigue...
In 1983 I was diagnosed with 'Mixed Connective Tissue Disorder'. I had some pain, but had extreme fatigue.
IN 1990, at age 43, I had a 'flare up' and saw a rheumatologist who diagnosed FM.
What a relief to finally have a definitive diagnosis!
All these years I have had occasional flare-ups...
Hi there,
I tried to do a search so that I didn't duplicate this post, but I did not see one, so I apologize if this is already out there.
The question I have, is does anyone experience an almost narcolepsy feeling during the day. I mean fall asleep wherever you are at the drop of a hat? It...
Hello, I was diagnosed with fibro in March 2015. I have a family history of ehlers-danios with my grandfather,mother,brother,uncle and cousin. I have a few symptoms similar to some of theirs but was never diagnosed. Have dealt with fibro pain for a few years before finally getting a diagnosis...
Hi everyone! This looks like a good site, glad I found it, I have mainly PTSD and Fibro and have had the worst year ever. Have had PTSD since I was very young and about 30 years ago was diagnosed with fibro, Ive had flare ups but this year has me at an all time low.also unmanaged depression...
Hi everyone! I was diagnosed with both fibro and peripheral neuropathy last year and have since been following the forum, but not posting. Just gathering info from as many sources as possible- not that I can remember it! Memory and exhaustion are terrible. Being a hairstylist, a new salon...