fibromyalgia and slash or me slash cfs 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 "fibromyalgia and slash or me slash cfs"

reset
How To Find Friends On Here That I Already Know
A MyFibroTeam Member asked a question 💭

I want to add my spouse to my team and i know another person that lives also has this app and i can not fond them so i can add them. Any suggestion on how find them or so they can find me. Thanks

•
View reactions
A MyFibroTeam Member

Go to the three lines on the top right. Go to meet others . Then put you zip code. People near you will show up. Click on person add to your team! Hope that helps! Hugs

Should I Get A Medical Id Bracelet For Fibromyalgia?
A MyFibroTeam Member asked a question 💭

Do u have to have an illness worse than fibromyalgia to get a medical id bracelet? Or, can it be for something like this illness plus others.

•
View reactions
A MyFibroTeam Member

I have a medical alert bracelet saying about me having fibromyalgia and allergic to surgical tapes.

It Stopped My Headaches
A MyFibroTeam Member asked a question 💭

Iv had the daith piercing for nearly a year and my headaches/migraines have stopped completely but my fibro is still the same as before.. I don’t take any medication for my fibro as it was making me worse, no harm in trying the daith. What may work for some doesn’t for others..

•
View reactions
A MyFibroTeam Member

What is daith piercing????????

Has Anyone On This Website Been Diagnosed With Both Fibromyalgia And Chronic Fatigue Syndrome? If So How Was This Diagnoses Reached?
A MyFibroTeam Member asked a question 💭
•
View reactions
A MyFibroTeam Member

Jodi Holleran & everyone! The difference between Fibromyalgia & Chronic Fatigue Syndrome is: that (CFS) is excessive tiredness. You’re dragging yourself to move, when you haven’t done anything. I… read more

Is Anyone Using DHEA To Help Alleviate Symptoms?
A MyFibroTeam Member asked a question 💭

I read that DHEA can help lesson pain. Has anyone else tried this and if so is it working? I already take mega doses of Vit D, Vit B, Q10 and Magnesium and also wear a magnetic bracelet! Will try anything other than the usual fibro "meds" at this point.

•
View reactions
A MyFibroTeam Member

I have a few items to suggest, one is: Zyflamend, another is LDN, more necessarily later.... uber busy today... but Dr. Jacob Teitelbaum has some to recommend... see his FB for his 'Pain' Book in… read more

Has Anyone With Fibromyalgia Or CFS Experienced Weakness In Hands, Arms, Such As Lifting Them Over Your Head, Leg Weakness?
A MyFibroTeam Member asked a question 💭
•
View reactions
A MyFibroTeam Member

Yes I hate it

Is There Anything Special Happening May 12, International Fibromyalgia Awareness Day?
A MyFibroTeam Member asked a question 💭

Does anyone know of anything happening online tomorrow May 12?

•
View reactions
A MyFibroTeam Member

Im sorry i missed it!

Anyone Live Near Raleigh,NC Who Has Received Social Security?
A MyFibroTeam Member asked a question 💭

I finally have a hearing date for June!! Anyone live near Raleigh who has been through the process? How did you fare? I'm using a lawyer from the advocator group.

•
View reactions
A MyFibroTeam Member

A good 'Tool' is a "Functional Capacity Report" via a Doc which details what you are NOT able to DO, RELIABLY (this can't hold a steady job)... contact me backchannel for assist mrst2222@… read more

Numbness
A MyFibroTeam Member asked a question 💭

Has anyone ever experienced having numbness on the lip? I do have nerve damage in my hands and here lately, the right upper lips has a tingling sensation and it goes numb for a little while.

•
View reactions
A MyFibroTeam Member

All great info. I haven't had facial numbness, but limbs, yes. I agree that meds can be huge contributor to individual symptoms. But I also agree that a pro-active measure to test various odd or new… read more

Fibromyalgia/CFS/ME Support Groups
A MyFibroTeam Member asked a question 💭

Do any of you lovely folks have local support groups? specifically for fibromyalgia/cfs/me? and how did you find out about it? doctor referral or on your own? sorry thats more like 4 questions!!

A MyFibroTeam Member

No