What Kind Of Pain Do You Experience? | MyFibroTeam

Connect with others who understand.

sign up Log in
Resources
About MyFibroTeam
Powered By
Real members of MyFibroTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
What Kind Of Pain Do You Experience?
A MyFibroTeam Member asked a question 💭

I'm newer to fibro and was wondering if people can be more specific when they say "pain". I'm having a hard time accepting this diagnosis. I have sharp- bee string like pains/ needle picks, burning, very heavy arms and legs and sore muscles. Tingling/vibrations. Aching hands/feet/ shoulders, wrists. Its just so many symptoms!!

posted February 3, 2016
•
View reactions
A MyFibroTeam Member

It's so hard when people don't take it seriously especially those close to us!!

posted February 3, 2016
A MyFibroTeam Member

a "flare -up" happens when things begin to settle down & you have reached a level when you can have times that are easier to cope with & more balanced , through pacing yourself & resting, & then something happens physically emotionally or mentally to upset that balance & your pain etc returns with a vengeance commonly known as a "flare-up " <3 There will be days to come where you do begin to feel a bit better or a bit worse ,it's all part of this dreadful illness .Thoughts & Prayers with you <3 Bless you & your Family xxxx

posted February 3, 2016
A MyFibroTeam Member

That's about right with Fibromyalgia ,or should I say wrong ! The Pains you describe are all "Normal" for Fibro .There are just so many different sorts of pain unfortunately. I have been living with Fibro for well over 10 years now :( .Another thing that is debilitating is the "Fibro-Fog" where your brain just refuses to work . Please learn to Pace your self ,try not to do too much when you have a good day ,rest when you have a "flare-up", when the pain & immobility are at their worst & keep in touch for support when you can . Thoughts & prayers with you at this difficult stage of readjustment & learning how to cope .xx

posted February 3, 2016
A MyFibroTeam Member

Thanks for your support. I feel like I've been in this "flare up " stage for months. Probably from all the worrying and wondering. Its always a symptom or 5! I spent nearly a year thinking I was dying of a brain disease or something. I actually had a bunch of xrays today and a EMG. Hoping the results are normal. I've had so many tests and blood work and everything is "normal". It just doesn't make sense how this disease can his from science. I just don't think anyone takes me serious. It's frustrating.

posted February 3, 2016
A MyFibroTeam Member

Yes, yes, yes, yrs , yes etc
You will be able to separate the different symthoms.

posted February 3, 2016

Related content

View All
Shingles
A MyFibroTeam Member asked a question 💭
Sensory Axonal Neuropathy
A MyFibroTeam Member asked a question 💭
Does Anyone Know The Different Beteen Arthritis/ Nerve Pain And Fibro Pain?
A MyFibroTeam Member asked a question 💭
Continue with Facebook
Continue with Google
Lock Icon Your privacy is our priority. By continuing, you accept our Terms of use, and our Health Data and Privacy policies.
Already a Member? Log in