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MS Society program

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I have been reading posts on this forum for some time, and am very happy

to have a place to go for information. I have ordered Revia from Mexico,

and will start as soon as it arrives. (I was unable to find a doc who

would prescribe.)

I have recently joined the board of the local MS Society (Omaha,

Nebraska), and am on a committee organizing a symposium to combine with

the annual meeting in October. I have been told that the new national

president is much more open to consideration of " alternative "

treatments than was her predecessor, and we hope that she will attend. I

would very much like to have someone come and speak about ldn. Who would

you recommend, and how do I get in touch with them? We expect about 200

people to attend the meeting, and while that's not a lot of people, it

would be a way to spread the word to at least that many more folks.

Thanks in advance for your suggestions.

Leatha

leathaj@...

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