Hello Everyone,

This is my first post. I was diagnosed with CIDP in 2005. What started as intermittent tingling in my right foot ended up with me in a wheelchair a year later. My neurologist put me on Prednisone 500 mg a week. Fortunately, with therapy and and great alternative treatment (G.E.T ) I've been able to have my Prednisone dosage lowered to Mg per week( now 2012). I pursued the G.E.T (glutathione enhancement therapy) as a means of protection from side effects of Prednisone and to balance my immune system. Now i walk with a cane. So, i sympathize with the many individuals who's experiences i have read.