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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.

Top 10 Search Results for "Unable to answer"

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Phantom Itch
A MyFibroTeam Member asked a question πŸ’­

Does anyone else have a severe problem with phantom itching? If so do you know of anything that will help?

A MyFibroTeam Member

I was going nuts from itching. The only thing that works is putting ice on for about 15 minutes. I have tried numerous medications & OTC stuff but nothing work

This Is An Answer To The Group For A Question I Asked On My Book.
A MyFibroTeam Member asked a question πŸ’­

Hi everybody, This is not a question but rather an answer. The question was, would you like to have my book Graceful Agony come out in paperback?

I still have your answers to answer myself, but I appreciate your replies and hugs and comments thank you.

Graceful Agony will be coming out in paperback and will be like the e-book international. My family comes from the UK and some in Norway and I have many international connections throughout this site and on social media. Again, I thank you… read more

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A MyFibroTeam Member

We have hit #1 3 times and a 5-star through Readers Favorite. So, I would love it for anyone who can read it. Thank you very much!

Tips For Navigating This Site
A MyFibroTeam Member asked a question πŸ’­

In conversations on this site I've seen some great navigation tips. Could we add the things we've discovered here so everyone can learn from each other?

For example search for the Q&A titled "Questions& Answer Links Tip" (which is a did-you-know about clicking the Q&A tab on the menu vs. the Q&A tab under your profile.)

My ex: when you have a question to ask, it seems you'll get many more answers by posting it on the Q&A board than by just posting it on your profile page.

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A MyFibroTeam Member

Ohhh, Janet, that is a great tip! LOL πŸ˜†πŸ˜†πŸ˜‚πŸ˜‚

Has Anyone Tried Thiamine For The Numbness And Tingling
A MyFibroTeam Member asked a question πŸ’­
A MyFibroTeam Member

Be nice if we could get some solid answers finally. I mean I just saw yet another new med for boner pills and I'm like- my body hurts too much to even think about sex these days, and now there's 4 or… read more

Have You Tried Visiting A Chiropractor For Fibro?
A MyFibroTeam Member asked a question πŸ’­

I'm thinking of giving it a try but my dad says they just want my money, if only he realized how much I needed to hold onto some hope into finding some answers. I'm not satisfied with this fibro diagnosis, leaves more questions than answers even after all these years.

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A MyFibroTeam Member

No giggles allowed.
We are doing serious business here.
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How Many People Hide Their Pain Or Hide The Fact That They Have Fibromyalgia?
A MyFibroTeam Member asked a question πŸ’­

The other day, someone I have known since childhood asked me to explain what it was like to have fibromyalgia as she has a relative with it and would like to understand better. Once I candidly explained what it was like, the reply came back that my symptoms must be much, much worse than the people she knew with it because she can only sometimes tell that it is bothering them. My answer to her was this. Please be aware that people with fibromyalgia are so tired of having people disbelieve them… read more

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A MyFibroTeam Member

Fibro is like getting hit by a Mack truck while running to the end of a 25 mile marathon,with the flu, and being 8 months pregnant. That'll give them something to think about!

Flair Ups
A MyFibroTeam Member asked a question πŸ’­

Please let me know how often you guys have a flair up.
Do you have varied flair ups ?
How often ?
Are you getting better ? Do you think your getting worse ?

I know the answers for me, it would be nice to hear what others have to say .... I feel like I'm in this on my own xxxxx

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A MyFibroTeam Member

Every day is different, my pain is daily but have some better than others I am on a recent change in meds which seem to work some days and not others already using amitriptyline, pregabalin, with tr… read more

If You've Been To The Mayo Fibro Clinic In Rochester, MN. I'd Like To Hear About It. I Am Set To Go In June, Am Hoping It Is Worth It.
A MyFibroTeam Member asked a question πŸ’­
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A MyFibroTeam Member

Hi summer I live in Michigan been to the Mayo Clinic years ago for complex regional pain syndrome (CRPS) it’s a very nice place. Chronic pain, fatigue, brain fog, unable to sleep I always thought it… read more

Would Someone Please Explain This, Is Fibro Autoimmune Or Not?
A MyFibroTeam Member asked a question πŸ’­

I found a question and answer on Google that just doesn't make sense to me. First I read that it may be different in different people,, meaning (?} that it could be autoimmune. Then it says Fibro is not autoimmune, which I thought it is. So, here's Google's answer.

Is fibromyalgia autoimmune or neurological?

They may be different in different people. Current research suggests involvement of the nervous system, particularly the central nervous system (brain and spinal cord). Fibromyalgia is… read more

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A MyFibroTeam Member

From what I understand it is not autoimmune. It is neurological and muscular. But, I am no expert.

Is Having Scalp Tenderness A Symptom Of Fibromyalgia?
A MyFibroTeam Member asked a question πŸ’­

I just got diagnosed a few weeks ago with Fibromyalgia. I have had scalp tenderness on and off for years. I've talked to a few of my doctors about it. No one has given me answer.

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A MyFibroTeam Member

Such good advice. I try to take care if I have any problems. Thank you
I do have IBS. WOW. They reclassified it. Yes, most people have no idea when I say I have Fibro. But some do. IBS comes and… read more