Im here ten months later and waiting to finally see a neurologist in March. I’m in so much pain. All my symptoms started immediately after a surgery late May 2024. After what I believe now were several red herrings I will see a neurologist. I suspect CIDP because of the symptoms, onset, progression. The last month has been a drastic decline I believe due to significant external stressors. I’m scared. I know doctors don’t love when patients diagnose with Google so I’m on the fence about mentioning my suspicion of CIDP mostly because if I’m wrong I don’t want to bias the neurologist. Thoughts? Thanks for this post and to the folks who commented on it and I hope you’re all finding some relief.