How many had ME/CFS diagnosis and years later feel its MS
I have had ME/CFS for 20 yrs...waiting to see neurologist as my symptoms seem to fit MS more so now that years have past and it's like now I have every symptom going. I think I was misdiagnosed and now I'm 20yrs in and really struggling.
I have FM since I was 20 and diagnosed with MS at 47. FM may have delayed the diagnosis due to overlapping symptoms. So I can understand that. You need that first step MRI. I have chronic migraine so I was already getting them when they found lesions. The neurologist may agree to rule MS out or other conditions. I hope your wait there isn't much longer