I have CIDP. 41 years ago, I was diagnosed with GBS after giving birth to twins. 38 years later, I had symptoms again and after 12 months was diagnosed with CIDP. Every 6 weeks, I have IVIG. Relapses occur, some worse than others. At least this immune disorder is not lfe threatening but life changing. I'm better off than many people. Stay positive.
Mark, how has your recovery gone since your stem cell replacement? It looks like it’s been a couple of years, was hoping to get an update on your recovery. Wondering if you would recommend the treatment and facility. I would really appreciate any input you have. Thank you.
How are you doing currently? I’ve been diagnosed with CIDP, it’s been a pretty scary 6 months. Unfortunately I’m not getting better with my current treatment.
