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
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
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.
I have a medical alert bracelet saying about me having fibromyalgia and allergic to surgical tapes.
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..
What is daith piercing????????
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
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.
Yes I hate it
Does anyone know of anything happening online tomorrow May 12?
Im sorry i missed it!
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.
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
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.
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
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!!
No