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Hi,

I'm Jen and I was just dx in Oct 03

I was put on Copaxone in Dec and it was not agreeing with me much so

I started to talk to others here on the net about alternatives.

A great guy by the name of Dave directed me tio this site.

I was scepticable but I too took this info to my neuro who not only

would not look at it but told me that it was a type of chemo and

other misinformation.

I researched further and went to my GP.

He read everything I had to offer and he agreed to try it with me.

I stopped Copaxone on Jan 12/04 and I have since been on LDN only.

I was on other meds for restless leg syndrom and since have stopped

taking those as well as I do not have the RLS anymore.

I have better thinking ability and balance and I now have enough

energy to work out everyday which I have been doing for 30 mins each

night after I work a full day and take care of my 3 year old

daughter!!

So does this work I say yes!!!!

2 months ago I could not do any of this and could hardly form words

to read a story to my daughter and now I can do it all!!!

As far as I am concerned you have nothing to loose and everything to

gain and this is the least invassive drug I have ever found for MS

and it works better then the crabs.

Hope this helps

Jen

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