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Body symptons

Does anyone get sore back shoulders arms buttocks legs. Bones feel achy burnibg skin and sore teeth and tongue.

tags: I also get sore ears and heat pains through my body

posted about 2 hours ago by A MyFibroTeam User
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All of the above and add an elephant sitting on your chest and burning eyes!!!

posted about 1 hour ago


Just courious....who lives or works near those large power lines that track for you can hear vibrate? Trying to see if its a common thing among us.

posted about 2 hours ago by A MyFibroTeam User
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We are more sensitive . Like for instance at work l can't go on certain floors cause the air condtioning units cause of the virbrations.

posted about 1 hour ago

Wheelchair tips?

Time of the month plus busy week equals fibro flare. Considering my wheelchair for college tomorrow, but I struggle using it. Any advice?

Thinking of doing what I always do - dive right in. Once I start I have no choice but to keep going. Just nervous doing that with a wheelchair!

posted about 4 hours ago by A MyFibroTeam User

Fellow fm suffers

Have you ever disclose that you have fm only to be given the "yeah yeah I was diagnosed with that too!" My current supervisor did this to me. I was just too through. My respect for her went out the window. The insentsivtivity of it all. ( sorry not a great speller)

posted about 5 hours ago by A MyFibroTeam User

I worked for a Judge for long time & as my fibro was getting worse. I followed up with my doctor, who immediately put me on a 30 day medical leave. When I return… read more

posted 1 minute ago

Exercise or rest???

I'm so confused and torn by things my doctors and physio keep telling me. They keep stressing the importance of exercise but tell me not to do more than I feel able to. Even just walking from work to the bus stop I feel like my back will snap with the pain or my legs will give way with exhaustion. Do I push through and do more or do I listen to my screaming body and rest? How do you guys cope?

posted about 7 hours ago by A MyFibroTeam User
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I use to push myself not realizing how much I was doing til I stopped. I say light stretching and rest. I know I should exercise more but right now walking is all I… read more

posted about 7 hours ago

Seven point five

Hey all you good people.. Have anyone heard of seven point five's medications and does it work?

posted about 8 hours ago by A MyFibroTeam User
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I'm lost

posted about 8 hours ago

wat foods to eat and aviod

Can anyone recommend wat foods are bed too eat and which ones too avoid. I have been told that soya products are good for fybro?

posted about 9 hours ago by A MyFibroTeam User
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Check out the Autoimmune Paleo diet... I've been on it for a year now and my Fibro symptoms are gone.

posted about 7 hours ago

Three year flare up?

I meant to ask before I went on vacation, but when I went to the pain clinic and explained how I'll I have been, the doctor said I have been having a flare. That means since April 2014, she thinks I've been having a flare. Has anyone else been told this? It's like she brushed off the worsening of my symptoms as if I will recover. If it's a flare, I'll get better attitude.

Plus I have CFS/ME, so suffer from PEM and she told me to walk briskly every day! Really???!!!

posted about 10 hours ago by A MyFibroTeam User
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I am so sorry you have to feel this way but I too have been having really bad flares going on 2 months it's gotten to the point that I sometimes cannot get out of bed… read more

posted about 8 hours ago


Has Prozac helped anyone's pain or fatigue?

posted about 14 hours ago by A MyFibroTeam User
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Prozac helps with depression but I can't see where it would help with fatigue. It might help with pain to a degree because it helps with the depression. These are just… read more

posted about 6 hours ago
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