Diagnosis
Hi all just wondering how u was all diagnosed with fibromarelga what test there was if any and how long it take thank u reply would be good please
The first diagnosis of Fibro my daughter was given was after two years of seeing medics. The doctor who diagnosed it went on symptoms and diagnosed her with CFS/FM. Many years later (and in a different country) she saw a rheumatologist who told her she has Fibro after a medical examination. Numerous blood tests and physical exams ruled out other illnesses. It's been a long journey (17 years ) with no pain relief from numerous meds/alternative therapies.
There is an expensive test that I am not sure most insurance pays for just yet. Otherwise the doctors eliminate other diagnoses/reasons for pain to come to a fibromyalgia diagnosis.
@A MyFibroTeam Member is a test called ANA that they do now that will show autoimmune disease. Then the doctor has to figure out which of the autoimmune disease you have. Such as Fibromyalgia,Lupus, MS,Lyme disease. It's worth finding out.
8/6/17
I've had that done cos I have slipped disc and sciatica to
I have itchy skin along with the muscle pain and knots all over my body
Does Anyone Else Have Raynaud's Syndrome In Their Hands & Feet ? Does Anyone Else Have Brain Fog ?
Overlapping Illnesses
Has Anyone On This Website Been Diagnosed With Both Fibromyalgia And Chronic Fatigue Syndrome? If So How Was This Diagnoses Reached?