If it's on your mind and it has to do with multiple sclerosis in any way, post it here.
I asked my doc if heard about LDN and he said no. So I asked about naltroxone. And he basically shrugged it off and didn't pay attention to me. I really want to try LDN I have a good feeling about it, but I have a bad a feeling I won't be able to get it. I definetly cant afford those 200 phone calls to prescriibng docs.
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tyr in my limited experience it helps to lay a lot of science in front of doctors. ie peer reviewed journal article abstracts with relevant phrases highlighted.
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Most doctors poo-poo LDN, but it has helped a lot of people. If you call Skips Pharmacy in Florida, they can give you the names of doctors who prescribe it. Some will consult with you over the phone.
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