A little update on me..

Well, I’m still trying to beat this thing I’ve got…Went in for a ncv/emg test yesterday and results showed worse than first one back in December..I pretty much knew it would be since I have been getting number and had other weakness tingling issues..My question is, what is the best type of ivig type and most effective treatment..Plasmerises (spelling)…Any feedback is helpful..I have been kinda slowly declining since 1/1/07..I came down with this novem 1/06 gbs (they diagnosed)..I’m wondering if the ivig 5 doses didnt totally overwhelm my bad immune guys, and have some residual relapse? I’m not 100% sure they will go with ivig, but almost positive…I see neuro tomorrow regarding results of ncv/emg..
I’m still trying to stay positive! deanop