anyone live in coastal north carolina and fibromyalgia | MyFibroTeam

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Top 10 Search Results for "anyone live in coastal north carolina"

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Lately, I’ve Been Getting A Weird Sensation In My Face. Do Any Of U Have This? If So, What Do U Do.
A MyFibroTeam Member asked a question 💭

I’m not sure if it’s neuromuscular or something else. I don’t think it’s anything to do with my mouth( dental work). God bless all u warriors!

A MyFibroTeam Member

@A MyFibroTeam Member do you have TMJ? I know a lot of people with fibromyalgia have it as well (Altho I had it decades before I had any symptoms of fibro)

How Do I Gently Let People Know That I'm Not Lazy In The Mornings. I Have So Much Trouble Getting Up When I HAVE To Be Somewhere, I Can.
A MyFibroTeam Member asked a question 💭
A MyFibroTeam Member

Can't we just taze them
I'm thinking it'd sink in pretty fast, lol
I take that back-

Omg- my big sister who was unbelievably sweet to take us (me and my kids) in and pay all the bills etc, has… read more

Hi, Has Anyone Travelled Over Seas With Fibro. I Live In Australia And It's A Long Haul Flight From Here. Any Suggestions About How To Cope
A MyFibroTeam Member asked a question 💭

I also have type 2 diabetes and have neuropathy. Sometimes I'm not sure which one I am suffering from. Thanks.

9 Ways to Naturally Improve Fibromyalgia Symptoms Read Article...
A MyFibroTeam Member

I have Type 2 diabetes as well Fibro and travelled to Pakistan . I live in UK . I found it so much better over there because of the hot country change of weather and dry air unlike UK which is always… read more

Vitamins???
A MyFibroTeam Member asked a question 💭

I have been reading up on vitamins that help fibro. Just wondering if any one in particular helped you??

A MyFibroTeam Member

I found a great one. It’s a water based vitamin mix - mix in water in the morning. It’s made for people with fibro and has higher levels of the vitamins that are believed to help with managing our… read more

Doctors That Specialize In Fibromyalgia
A MyFibroTeam Member asked a question 💭

Does anyone have a doctor in North Carolina that specializes in fibromyalgia?

A MyFibroTeam Member

Yes and it sucks!

Flare
A MyFibroTeam Member asked a question 💭

What are some of the signs for a flare up? I have lupus but have also been diagnosed with fibromalgyia. I'm trying to determine which is lupus and which is fibro?

A MyFibroTeam Member

It was a rash on both arms. It went away after several weeks and has never can back. My drs did testing for Lupus anyway it was all neg.

Ok My Lovies- As Requested And Several Been Waiting For- It Is Time. What Are Your Favorite Shows?
A MyFibroTeam Member asked a question 💭

Hit me with all of them.
Old- new
Finished series or canceled one. Any genre too!

Only loose rule I have is if you happen to know where it is , try and list that too.

So many streaming services and they all now make original shows and movies.

But it's a loose rule, I won't get out ruler and swat your hands or anything if you don't.

Ready, set, go!

A MyFibroTeam Member

I will chk it out

Hi I Had N Problem Yesterday Morning When I Wake Up. The Right Side Of My Face, Lips Included Were Dead It Takes An Hour Or To Be Normal
A MyFibroTeam Member asked a question 💭

After the face trouble I was feeling really sick Did anyone had something of that

A MyFibroTeam Member

Love hugs & good night all xxxx

Magnesium: Are Your Doctors Recommending Topical Or Oral? What's Working?
A MyFibroTeam Member asked a question 💭

Diagnosed several years ago(the works), taking amitriptyline which is a godsend. Still have hand pain. Going to ask my doctor about magnesium deficiency. See references here to oral supplements but it seems that other sites are recommending topical sprays or Epsom salts for better absorbability. What is your doctor recommending? Heard that oral is hard to absorb, and excess will lead to diarrhea.

A MyFibroTeam Member

I take my magnesium as powder mixed in water. It absorbs well this way and has not given me stomach problems.

What Causes Electric Zaps To Your Head
A MyFibroTeam Member asked a question 💭

fibro for over 30 years

A MyFibroTeam Member

People have talked about having them on support group but I never had them till just recently. Be careful with your eyes because they can.t be replaced. I hope you don't get that again but if you do… read more