so now what

WitHope…I understand all of what you posted..we have been dealing with CIDP in my family for many years, my sister has it. I am following her progression exactly..even the misdiagnosis! I just need to be sure I have ALL my facts straight when I go back to my new nuero. My MRI was of the brain and she is the one that stated there should be changes if what I have is CIDP…from everything I have read that is not the case……is that correct??? I ran all of this by my sister and she had the same opinion I did…the MRI of the brain is not an indicator of CIDP…she is at MAYO today and is going to see if Dr Dyke will look at my test results. I can only hope……