My experience with infusions for CIDP has been headaches when the drip rate is too fast. I'm very tired for 2 days afterwords but my energy increases and pain lessens.
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The IVIG treatments have helped me tremendously. I get a boost of energy every month, no side effects except a headache sometimes when the infusion rate is too fast. It also helps my pain levels from SFN which spike before montly IVIG treatments. It keeps my CIDP from progressing. It does take a chunk of time though, about 6-7 hours each day.
Sun, Jan 6 10:20am · CIDP (chronic inflammatory demylinating polyneuropathy) in Neuropathy
They help with energy and pain. I always know when it's time for my next infusions as pain increases. Is anyone having IVIG just for small fiber neuropathy?