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Hi I am new to this list and just recently diagnosed with RRMS.

I went to see my family Dr. today to see what type of info he had to

add to Neurologists suggestions etc.

I mentioned LDN to him and he said he had never heard of it and

could I get some info on it to him to take a look at. He is a VERY

open minded kind of guy.

I am wondering what/where the best info is that I could present to

him?

Also, I am wondering how expensive LDN is and if Insurance ever

covers it since it is not an FDA approved drug?

Also, if any of you know of a Dr. in the New England area who

prescribes LDN and could give that info. to me I would really

appreciate that.

Thank you!

Colleen

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