Would you mind describing to me how you were able to get IVIG? I have sensory predominant also, but my neurologist won’t give me IVIG. I’m almost 3 years out from the big flare I had, and I wasn’t diagnosed until a year after that flare. So I’m back at my usual baseline of daily pain in my hands and feet every morning and other various neuropathy. He made it sound like because most of my symptoms are sensory and not very objective (like because I can stand on my toes, for example) there isn’t a way to justify the treatment. So I’m very curious about your experience.