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My name is Margaret and I waS Dx with MS last August. I am doing

pretty well but want to know more about LDN.

I have heard wonderful things from people on my MS lists, yet thr MS

Society doesn't seem interested in endorsing it or finding a way to

do clinical trials. I am currently on Rebif.($$$?)

Is anyone taking an ABCR along with LDN?

What is your experience with this?

My worst Symptom is visual ON. Any luck with this on LDN?

Thank you all.

Margaret

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