November Update

I will have my third Cytoxan infusion this Friday, November 4, 2011. This is eight weeks into my six months of treatments. The Cytoxan is still less stressful on my body than either IVIG or PLEX and I have had no bad side-effects. Soli Deo Gloria!

My Myasthenia Gravis is no worse but no better than when I started the treatments. This is good because I am not worse. Breathing and vision are still real problems for me.

My Small Fiber Neuropathy is still worsening and hurts a lot. I am numb, tingle, burn, and ache all at the same time!

The good news is Social Security approved me for disability this week after only six months and one denial.

Thanks again for all the prayers and support. More later!