SCT at NW – Hope it is going well
Rosanna – Hope you are doing well with the SCT. 14 years is a very long time to have been afflicted with CIDP. My son had CIDP for 1.5 years when he had his SCT in Chicago. His symptoms got worse quickly and in pain all the time. SCT was his only option. He is great today – his feet are still numb but he can walk!! It is not overnight and everything you are going through is worth the gains you will make. Good luck with it – my son has a carepage that I wrote that was a pretty good chronology of what took place during the treatment time in Chicago. If you are interested, I will send you the link.