post-viral syndrome and fibromyalgia | 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.

Top 10 Search Results for "post-viral syndrome"

reset
Did Anyone Try The Polaraid Disk Treatment Yet?
A MyFibroTeam Member asked a question 💭

I think it's new...new to me anyways.

A MyFibroTeam Member

What is it?

Is Coffee (and Creamer) Hurting? Is Sugar Hurting Me? I Have Been A Sugar Addict All My Life!
A MyFibroTeam Member asked a question 💭

I like drinking it in the morning, and read some comments about stopping. I know sugar will have to stop, because I feel worse the next day. But I don't know for sure...

•
View reactions
A MyFibroTeam Member

I’m addicted to coffee. I slowly changed the amount of sugar in it. After a while I started to appreciate it without sugar. Switch creamer for almond or any other veggie sugar free milk and keep this… read more

Has Anyone Been Treated At Stanford Medical Center For FMS As A Post-viral Syndrome?
A MyFibroTeam Member asked a question 💭
•
View reactions
A MyFibroTeam Member

I found this post in the Epstein Barr virus as cause of FMS
Found this interesting read on the Epstein Barr virus and relation to fibromyalgia

Check out this article on goop.com. http://goop.com/t… read more

Itching Starts At Night
A MyFibroTeam Member asked a question 💭

Has anyone else (with skin sensitivities) noticed that their itching gets worse at night time? I hardly itch at all in the daytime but by 9pm, it starts and by 11pm it is really aggravating and by 1am, it is simply maddening. I've talked to one other person who has the same exact problem. I'm trying to find out why it gets worse at night.

•
View reactions
A MyFibroTeam Member

Happens to me also and I don't itch in daytime?

Do Anyone Have Trouble With Their Tongue As Hurts & Burn
A MyFibroTeam Member asked a question 💭
•
View reactions
A MyFibroTeam Member

I thought it was the side affect of my RA medicine. My doctor. gave me a high dose of Folic Acid prescription. That cured it within a day or so. You can always use this little remedy. Get a bottle… read more

Inner Ear Pains
A MyFibroTeam Member asked a question 💭

Does anyone have sudden, brief lived stabbing inner ear pains that come and go and are sometimes accomapamied by similar head pains? I am wondering what they could be.

•
View reactions
A MyFibroTeam Member

It is hard for me to tell over the train whistle lol.
But do get ear pain and the head pain is 24/7, just degrees and location change.

Regarding A Supplement
A MyFibroTeam Member asked a question 💭

I had heard about a supplement from someone on this site.
she just informed me that she was kicked off the site.
she did not advertise on the site.
she offered that if anyone were to be interested they could email her which I did.
I think this may be a little harsh, for I do think she was trying to be helpful.

•
View reactions
A MyFibroTeam Member

Yes, @A MyFibroTeam Member, always a good idea for us. Someone said to me, “Don’t borrow trouble “. I’ve always remembered that!

Does Anybody Have Any Other Illnesses, Diseases, Or Syndrome Along Wth Fibromyalgia?
A MyFibroTeam Member asked a question 💭
•
View reactions
A MyFibroTeam Member

I must go ATM
I have an appointment dear I'll be back after 6pm Perth time.
God bless

I Have Fast Heart Beat Of Up To 150 And Extreme Fatigue Together With Diziness.Am L Alone In This
A MyFibroTeam Member asked a question 💭

Does anyone has fast heart beat of up to 150 and extreme fatigue

•
View reactions
A MyFibroTeam Member

P. ostural O.rthostatic
T.achycardia
S.yndrome
blood pressure drops low, especially standing and heart rate Tachycardia in order to try to hurry some blood pumping to vital organs. Brain isn't… read more

Sjogrens Syndrome Sufferers
A MyFibroTeam Member asked a question 💭

I am told I do not have sjogrens syndrome, however I have very dry eyes and dry stinging burning lips and tongue. What do you do to relieve the dryness, or what do you stay away from because it aggravates the symptoms?

•
View reactions
A MyFibroTeam Member

Oh man! I already answered your post too.

When I review older posts and click I don’t see my answer. I only see it after I send a new post
My apologies. It tells me I have many unread messages so… read more