Reply To: Update one year after diagnosis with CIDP
PattyO you will get there too. I don’t understand why your doctor can’t prescribe the subcutaneous IVIG. Others over the years here on the forum have had it–well before it was officially sanctioned for CIDP. Sounds like it would be an excellent option for you. Still have those dinner parties and enjoy your friends. That is one thing I have learned from the ALS forum–you can still do everything you did before, but just in a different way. You are still that dynamo marathoner personality and great mom who happens to have CIDP which is treatable and you will get better like Marshall.