tag:blogger.com,1999:blog-3735039359206747030.post4086636188979388729..comments2013-11-11T13:27:56.165-08:00Comments on My life with CIDP: current 3/21/12Cherylhttp://www.blogger.com/profile/09147651906168686013noreply@blogger.comBlogger2125tag:blogger.com,1999:blog-3735039359206747030.post-11127461652240098812012-03-28T19:32:42.503-07:002012-03-28T19:32:42.503-07:00Hi Michael,
Glad you found me :) My favorite broth...Hi Michael,<br />Glad you found me :) My favorite brother's name is Michael, or as I like to call him "god" or St.Michael (family joke) Anyway, I am now down to 250mg of Cellcept daily and by the weekend I will be off it and only on IVIG & Steroids. I am praying it works well for me.Cherylhttps://www.blogger.com/profile/09147651906168686013noreply@blogger.comtag:blogger.com,1999:blog-3735039359206747030.post-77958308697860990702012-03-22T19:33:01.968-07:002012-03-22T19:33:01.968-07:00Hell, I just found your blog tonight. I was diagn...Hell, I just found your blog tonight. I was diagnoses in 2010 and am currently taking the prednisone/cellcept cocktail, with periodic IVIG infusions. They helped be bounce back and I seem to be doing alright except for massive fatigue and all sorts of pains. Well, I have nerve damage too so I have to walk wioth ankle-foot orthotics. I am hoping we will continue the med reductions. I am also worried about the long term effects of the prednisone and cellcelpt, but I know that without them, I never would have gotten out of the wheelchair.<br /><br />Please feel free to check out my blog, the link is in my profile.<br /><br />Michaelmwilliams1220https://www.blogger.com/profile/13584142934595165752noreply@blogger.com