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#1 | |||
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If I ever get IVIG i sure hope it works. No other options really. And I got scared of prednisone after seeing a bunch of youtube vids about it. No thank you! My first neuro prescribed me 60mg daily! After doing my research I tossed the prescription out.
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#2 | ||
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My IGG and IGM were both very high, and I was on IVIG. The IVIG was used to modulate the immune system in my case.
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#3 | |||
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#4 | ||
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With IVIG, plasmapherisis and rituxin it is believed the immune attack on my nerves was stopped.
I'm not 100% sure which one stopped it, or if it may have been the combination of them all. I did not "get better" or regain any lost nerves. I just stopped progressing, with the nerve damage staying in my lower legs/feet. |
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#5 | ||
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Quote:
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#6 | ||
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Quote:
I'm still afraid that it one day might progress, but try not to worry or think about it unless it starts happening. |
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#7 | |||
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Seems IVIG is tough to get approved by insurance. How do people get approval for PN if its not CIDP or MMN? Those seem to be on the "approval" list for most insurance companies. Is there a workaround?
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