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Been on LDN since July 2004

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Been reading everybodies posts since July 2004. I thought it was time to share

a little

about me. I was Dx'd with probable MS June of 2004. I have been on LDN since

July 2004

after reading about it on this site. This of course was against the advice of my

Nuero. I

am doing really good since taking LDN. No more fatigue, no more skin

sensitivities, less

brain fog and no progression. Still get tingling/buzzing in my hands and feet

when under

stress plus at times they can get very hot. The tingling/buzzing/hot were some

of the very

first symptoms that I had. Apparently they are here to stay. Anybody have any

ideas on

how to solve or lessen that problem aside from avoiding stress?

Thank you all for the information you provide on this site.

You guys are all AWESOME!!!!

Keep up the good work!!!!

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