← Return to Has anyone had IVIG Infusions for Neuropathy?

Discussion

Has anyone had IVIG Infusions for Neuropathy?

Neuropathy | Last Active: May 29 7:12pm | Replies (422)

Comment receiving replies
@roslyn2314

When I read some of the comments especially yours and realise I’m not that bad off .
All the best for your your on going journey with trying to maintain some degree of health ..

Jump to this post


Replies to "When I read some of the comments especially yours and realise I’m not that bad off..."

I am talking about my journeys and frustrations hoping. No one has to endure what I am going through. To be the told for years I have essential tremors to find out instead it’s related to neuropathy. Why hasn’t anyone treated me for neuropathy knowing that in the past I was on IVIG therapy. I have lost muscles in my feet and legs. It’s frustrating. The only thing that has the doctors moving is Dr Oaklander telling them that I should not be in the shape I am in. Now since I am supposed to follow-up with her in a year doctors have decided to get off their lazy duffs and do something. If I can document my journey and the doctors finally find out what is wrong with me then maybe it will help someone else.