Reply To: Random questions for those who have CIDP

Thank you JK! I went ahead and ordered some compression socks anyway–I figure they can’t make anything worse. I’m praying that my protein comes back high so I can start the treatments. My neurologist told me my treatments would be home based so that’s good. It is my understanding that with treatment (should it work and I’m hopeful that it will) that my symptoms will never get worse then they are now, but will get better. Is that true from your experience?