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Has anyone had IVIG Infusions for Neuropathy?

Neuropathy | Last Active: Oct 3 7:57am | Replies (491)

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@efgh1020

After a long diagnostic process, 2 neurologists concluded that My polyneuropathy was probably an autoimmune reaction to either spinal fusion surgery, infection unrelated to the surgery, medication or anesthesia, or some unknown factor. I had been screened out of other antibodies, and am not diabetic nor did I have chemo. That meant I could be covered by Medicare Advantage for iVIG treatments. Over the last year, they have added to my strength and range of motion. I am resuming them after a fall and fractures which have healed. I have skepticism about the cited Dutch study with only 60 participants, done from 2016 to 2018. I think any study needs a wider population of subjects. At my neurologist’s suggestion, and my own good results earlier, I am continuing the iVIG treatments. With an antihistamine before the immunoglobulin IV insertion, I have had no allergic reactions.
If approved by a neurologist, I recommend iVIG treatment to reduce inflammation of the nerves.

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Replies to "After a long diagnostic process, 2 neurologists concluded that My polyneuropathy was probably an autoimmune reaction..."

Hi @efgh1020
I am having an IVig in 30 minutes so I will say more later. I have neuropathy, I do so many things to relieve the symptoms, if you would like that list, I can post it again. My neuropathy increased in severity after severe allergy reactions, just to add to the 'could it be autoimmune' even though I have had chemo.