My demylenation progressed rapidly and a couple of months of incomplete DX and inadequate treatment cost me significantly.
I didnt get a complete DX or begin correct treatment until I found the right neurologist.
My current neurologist is a [COLOR=”black”][COLOR=”Red”]neuromuscular [/COLOR][/COLOR]specialist who has treated CIDP.
Fortunately for me there are multiple university hospitals here with multiple specialists so I didn’t have to hunt long or travel to find the right one.
A neurologist who specializes in neuromuscular disorders and one who has treated CIDP might be your best bet.
Push, push, push, don’t allow delays or 3 more months to go by and settle for seeing the same neuro. From what I’ve seen and experienced time is of the essence.
I prayed for you today.