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.

MrGSH,

It is great to have you come and be with us. You will fine a great number of dear friends to listen when you are in need of ears. Please let us know how we can help you out. You will find out we are supportive and relaxing place.

Please keep us up to date on your condition. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you.

Darlene