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I don't post very often but tonight is night 170 for me on LDN and I

have nothing but great things to say about LDN!

I had my first MS incident was in 2001. I had a bunch of tests that

were inconclusive. The symptoms went away and I never thought of it

again until April '03 when my hubby was in Iraq. My feet went

numb/tingling as did other unmentionable parts of my body. It was

enough for my neuro to get my beloved home. With steriods, I went

back to normal except for my feet and fatigue. I did have another

flare-up in May of this year just before I started LDN but again that

was pretty mild with just my left hand and left side of my torso

going numb. I overreacted and I got steriods cause we were going on

vacation. Never again... I became pyscho mommy/wife.

Up until two weeks I was on Copaxone. I had been on Avonex for a

year before I started LDN but my neuro wouldn't give me LDN without

me on something else so that's why I went to Copaxone. I just up and

decided that I didn't need the Copa anymore and now I can say I'm

CRAB free and happy about it. I am sleeping better, my fatigue is

gone as much as it can be with three activity-involved children.

Also, just today while driving I realized my feet are almost

completely back to normal. My life is good!

Thanks for letting me share and for all the great info and support

this group gives.

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