who feels like their symptoms are getting worse and fibromyalgia | MyFibroTeam

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Top 10 Search Results for "who feels like their symptoms are getting worse"

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Does Anyone Else Feel That Their Fibro Symptoms Have Gotten Progressively Worse Over The Years?
A MyFibroTeam Member asked a question đź’­

Hi fellow fibro warriors. Lately I've been feeling like my symptoms are worsening over the years. Pain is getting worse as is forgetfulness and anxiety. I'm afraid to drive or go anywhere by myself. Seems like I'm having less and less "good days" and sliding down fast. Not sure if this is a real thing or just my imagination.

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A MyFibroTeam Member

Not your imagination at all. This disease more often than not continues to progress. Maybe we should all go after big pharma. They’re making way too much money to even look for cures, just like… read more

Thank You For The Add. Hope You Are Having A Good Day
A MyFibroTeam Member asked a question đź’­
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A MyFibroTeam Member

It's not a stupid question but a very relevant one. Despite Medical Experts stating otherwise. I personally find it does worsen with age. My mobility seems to decrease more and more as I get older… read more

How Would You Describe You Fatigue To A Non-fibro Sufferer?
A MyFibroTeam Member asked a question đź’­

I suffer with fatigue more than pain, or maybe I manage/cope with the pain better than I cope with the fatigue.

I have well-meaning friends who say things like “how’re you sleeping” or “have you tried lavender?”... etc and I get so frustrated that people don’t understand, it’s irrelivant how much sleep I’ve had, it does not refresh me and I’m still fatigued, day in, day out, no matter what I do or don’t do.

One description I’ve come up with is “it’s so tiring to move and my body feels so… read more

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A MyFibroTeam Member

The best way I describe chronic fatigue is I feel like I was just administered anesthesia! I have fibro also so I'm in pain 24/7. Sometimes I can push through the pain but I have not found anything to… read more

Describe The Beginning Of A Flare Up
A MyFibroTeam Member asked a question đź’­

In the hopes of pinpointing the onset of a flare up-being new to this and all- what little clues have you learned to spot that warns you a flare up is coming? Whats the longest youve experienced?

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A MyFibroTeam Member

I usually have scalp pain

Stress And Memory
A MyFibroTeam Member asked a question đź’­

Does your brain fog and memory loss get worse under stress or is it consistent?

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A MyFibroTeam Member

Couldn't agree more with Suzie. Because we tend to get isolated and because of the possible inflammation in our CNS because of Fibromyalgia, we need to be very aware of brain health. Part of that is… read more

I Have Just Tested Positive To Covid And My Fybro Symptoms Seemed To Have Increased. Is This Common? Just Curious..
A MyFibroTeam Member asked a question đź’­
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A MyFibroTeam Member

I agree, I just believe my fibro caused me to have a very different reaction. My Sister had to have them because she works in healthcare and my Momma (may she rest in peace) was also almost 90 and… read more

Do You Ever Wonder If Your Diagnoses Are Correct?
A MyFibroTeam Member asked a question đź’­

I have been diagnosed with fibro, me/CFS and POTS, with me/CFS being the worst. I still manage to somehow function and raise my children, though extremely limited. I have had neighbors and family say that getting old is hard business (mind you I'm 30). I sometimes stop and wonder if really I could just "snap" out of this and maybe it is a mental issue. I know what I'm experiencing is real. And I most of the time am emotionally resilient. But sometimes when I am pacing I wonder, maybe I'm setting… read more

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A MyFibroTeam Member

21 years ago I feel, I injured my leg after I had surgery on my knee I was diagnosed with RSD/CRPS it is also a nerve disorder but the burning pain is like I but my foot in fire it was very bad I’m on… read more

Does Anyone Get Exhausted And Depressed After A Simple Outing?
A MyFibroTeam Member asked a question đź’­

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

Hi everyone. I've just been reading all these comments. Wow I can relate to everyone of them. It's 4am here and I am up with jaw pain. I thought it's my teeth!! But now I'm thinking it's this… read more

Low Blood Pressure
A MyFibroTeam Member asked a question đź’­

I have been hearing people talk about a lack of oxygen to the brain being a cause of inflammation, etc. I've seen where some say hyperbaric oxygen can cure fibromyalgia. So as I looked for ways to increase oxygen to the brain (exercise is certainly one), I find where low blood pressure will decrease oxygen to the brain. Wow, I have low blood pressure. The other night it was 81/60, though it is usually 90/70. Do any of you have consistently low blood pressure? Cause maybe this is one path to… read more

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A MyFibroTeam Member

I've thought about trying Hyperbaric Chamber but insurance won't cover it arghhhh

Does Anyone Else Get Tongue Tied And Get Words Mixed Up?
A MyFibroTeam Member asked a question đź’­

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

I get this all of the time, thankfully those close to me understand that when I take a break in a sentence it's because I'm trying to find the right word
I also start to lose my voice if I talk a… read more