Reply To: Your Progression of CIDP
I sit here with my legs, arms, shaking and stinging..thinking how fortunate I am that I can still use my hands & legs. But, scared to death that as I sit here waiting on someone to approve a co-pay assistance for my IVIG treatments..things seem to be getting worse. Not sure if it is our extremely cold weather or just normal progression of the CIDP. If some others would shed some light on how their disease progressed it would be greatly appreciated!