Fibromyalgia

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Describe what a Flare Up is to you ?

Describe what a Flare Up is to you ?

We all speak of the dreaded " flare up" but do we all experience the same symptoms ? For my own curiosity I'd like to know what others call their flare up . A flare to me is my whole body filled with aching , burning , stinging relentless pain. My mind becomes cloudy, thoughts make no sense, speaking becomes hard because the brain and mouth aren't working together . Nothing takes the pain away, no amount of drugs, therapy or rest eases it, it's like the flare takes over and… read more

A MyFibroTeam Member said:

A flare up to me is the whole body or just any part of body. Like yesterday my shoulders flared up so bad i had go bed to keep warm. Today my body in… read more

posted 2 months ago

Finally, a solution to my pants!!! :) LOL

Finally, a solution to my pants!!! :) LOL

Comfort is not usually a word surrounding Fibromyalgia sufferers. But I have to tell you, I'm so happy that I have come up with this idea. Some of you may have already known this trick and maybe I'm the last one to know. But at a risk of sounding ridiculous, here it goes. I have suffered with the pain of fibromyalgia along with the rest of you. I must say, even wearing clothes gets painful at times. I especially dislike wearing shorts or jeans or skirts. Basically anything… read more

A MyFibroTeam Member said:

I love it! I've actually thought of trying on matenity clothes while passing the clothing area in stores, but you just gave me the courage to go for it!… read more

posted 9 months ago

Full time employment and fibro

Full time employment and fibro

just for my own sanity... How many of you lovely people have lost a job or more than one due to your fibro symptoms?

A MyFibroTeam Member said:

I managed to go short term disability into long term now, but it is very confusing. I can't get my head around all the info. The fogs are frustrating… read more

posted 2 days ago

How to help a friend with chronic illness

How to help a friend with chronic illness

There are many ways to reach out to help, and of course the needs will change for each person. Big things like helping clean the house or cooking meals can help, but often it’s the little things that are the best, like opening the door for them, or remembering not to wear perfume. Here’s a list of a few things that can help (with thanks to many other websites I‘ve read similar lists on over the years):

~ Don’t be afraid to hug her gently, but please no bear hugs.
~… read more

A MyFibroTeam Member said:

I think someone must have been keeping a log! You've hit so many of the things but I think of and of course I never have something to write it down with… read more

posted 4 months ago

Sweating

Sweating

Does anyone sweat with there fibromyalgia not just at night but during the day as well?

A MyFibroTeam Member said:

Just spoken to the Dr and he's now backtracking saying there's no specialist because I've already had a sympathectomy and apart from increasing the pro… read more

posted 15 days ago

Does anyone get exhausted and depressed after a simple outing?

Does anyone get exhausted and depressed after a simple outing?

Hi Everyone,

For years when I come home after being out I find myself sitting in my car for about an hour or more unable to move feeling exhausted and down. For a long time I thought it had to do with my PTSD but tonight I think it is due to fibro fog and fatigue??
Can anyone relate? Thank you in advance!

A MyFibroTeam Member said:

There are times I went out to go grocery shopping got to the store and sat in my car only to leave just because I just couldn't muster the energy. I… read more

posted 26 days ago

Does anyone else get tongue tied and get words mixed up?

Does anyone else get tongue tied and get words mixed up?

This has been a very busy week at work - my body isn’t so happy. My feet hurt even when I first get up in the morning. My left elbow hurts - it’s usually the first body part to experience pain.

What concerns me today though is that I’m struggling to speak properly. I’m getting words and letters mixed up like saying “baper pag” instead of “paper bag”. Does anyone else have this problem? It’s a bit scary.

A MyFibroTeam Member said:

sorry but that is part off are problem short term memory or no memory and problems talking trying to remember things is hard my memory is worse than a… read more

posted 9 days ago

I have read that depression can cause pain. I believe the opposite is true.

I have read that depression can cause pain. I believe the opposite is true.

I believe pain can cause depression.
I belive that pain limits what you can do. With those limits comes self worth issues and can also cause isolation.
What are your thoughts on the subject?
After all WE are the EXPERTS !

A MyFibroTeam Member said:

I shall Thank you

posted 19 days ago

Foggy brain

Foggy brain

What can I do to help with my foggy brain? I'm a nurse and get really embarrassed when I can't think of my words.

A MyFibroTeam Member said:

Where do you get carbon60?

posted 7 months ago

Does anyone else get pain like someone is sticking a pin in you

Does anyone else get pain like someone is sticking a pin in you

Its like a sudden jabbing pain like someone has stabbed you with a pin or several pins. Its is so embarrassing when it happens and I have visitors. We can be talking away and suddenly I will jump up and shout OUCH!.
I feel such a fool, they must think I am nuts.
When my guest asks what's wrong I just reply I think I was stung by a wasp. Cos that's kind of what it feels like. Does anyone else experience this sudden random pain?

A MyFibroTeam Member said:

Today is rough day for me. I had steroid injections due to accident that damaged my cervical and lumbar spine. Today I'm nauseous, stomach pain,… read more

posted 2 days ago
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