Reply To: New- CIPD and Central Nerves/ Cranial
Thanks Jim can you please tell me if PE is good for autonomic symptoms too? Excuse my ignorance but I am so new to all this that I haven’t got my head around the finer details yet )-: My neurologist wasn’t v optimistic about what I could expect in the way of improvements – seemed to suggest that the IVIg might slow down the progression of disease but that my nerve damage was too extensive to reverse any damage. Although my test results strongly suggest that I have had CIDP for a very long time (20 years plus) the cardiac issues and numb face etc are very new – maybe 2-3 months but escalating quickly. More advice please about my next steps would be v much appreciated.