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Another doc rejection

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I presented my neuro with all the info (thanks to all who made

suggestions). However, he rejected the idea, saying that all the

evidence was anecdotal, and that he could not give me a prescription

because it is not FDA approved for ms. Also, none of the compounding

pharmacies in Lincoln, Nebraska, have ever filled a prescription for

LDN, so they can't help me. I have an appointment with my gp, and will

see what he says. I'm also putting out feelers among other mser's in the

area to see if I can find a more open-minded doc.

One interesting thing that my neuro did mention - there is an LDN study

going on at the University of Iowa in Iowa City. I haven't researched it

yet - has anyone else heard of this study?

Thanks,

Leatha

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