Hi all. I was finally dxed in sept but had been experiencing terrible flares and misdiagnosis for long before. I am trying to motivate myself to get back to work but the fear of not being able to handle it or fulfill my obligations keeps holding me back. Does anyone else experience this? Has anyone overcome this? If so, what helped you overcome your fears? And what has helped you once you got back to work, especially when fibro flares up
Some days I feel really motivated to get back to my “old… read more

Donyou do yoga? Didbyou stasrt at a studio? I cant even touch my toes.... A friend suggested yoga. He says to do it at a studio tgough so there is a teacher to help a guide me through it.... Also so i dont get hurt.. whibwould think get hurt doing yoga?
Tell me about your experience with yoga please.
If tou know of a good place in north central Phoenix by some crazy chance let me know!

I was looking through the notes on my portal of the pain management doctor.. now I know what I've discussed with him, so I was just curious if anyone has been diagnosed with chronic pain syndrome... I googled it, but I always like y'all's input... (For insurance purposes I think he's using the diagnosis of chronic pain syndrome, but my pea brain thinks there's no difference between them!!?

hello everyone hope your all doing as well as you can . i was just wondering if anyone gets really bad pain and tirdeness from shoulders all the way down to fingers i have had the pain before but my arms feel so heavy that even brushing my teeth is hard and i also noticed my jaw is tired when i try to eat and cant seem to open my mouth very well its like the whole top part of my body is extremly fatuiged . sorry to go on everyone just wonder if any one gets this i have had fibro for around six… read more

I have seen that pelvic problems are well documented in women with fibromyalgia so I’m asking this question for the men. Does anyone else suffer with prostate/ bladder/testicular and rectal pain? I was told by the Urologist that I have a pelvic floor dysfunction and chronic prostatitis.

How many of you were born left-handed? I heard somewhere left-handed people have a part in the brain that is a little bit bigger(more nerves/ neurons).

I am just wondering if there is any truth to this theory that left-handed people are more likely to get nerve problems.

Again, it is just a theory.

Although fibro is defined as not being MS I feel that they appear so a like.. For example the tiredness and twitching of the muscles... I am interested in your views,my physio says it is an autoimmune disease... Any help out there as to what category fibromyalgia fits in to please xxxx

My finger tips feel frost bitten without being outside?