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CIDP (Chronic Inflammatory Demyelinating Polyneuropathy)

Autoimmune Diseases | Last Active: 2 days ago | Replies (340)
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@shainahshadow

Yes definitely as that is the only thing I have is infusions of IVIG.
I wish there was a support group for CIDP AND SJOGRENS near me.

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Replies to "Yes definitely as that is the only thing I have is infusions of IVIG. I wish..."
harley22 | @harley22 | 4 days ago

I had 8 mos of IVIG infusions and didn’t feel any relief from them,so I stopped them.
No sense continuing them if they weren’t helping me.
In March I will be starting a new infusion recommended by my neurologist called Rituxan.
It’s given in his infusion center 2 infusions 2 weeks apart then again in 6 mos
I hope this works

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