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New LDN MS Patient

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Greetings,

I've been taking 6mg of LDN for just over two weeks. I've read quite

a bit on the website about LDN and M.S. and was hoping to talk to

others who have M.S. and have been taking this medication. I've taken

Copaxone, Avonex, and an experimental medication over the last 10

years since my diagnosis. The medication that had worked the best for

me was the experimental medication that I've taken since December

2005. It has been miraculous but it is no longer being made and I've

had to investigate other options. I really didn't want to try the

normal M.S. drugs since they really don't seem to do much more than

have many side-effects and somewhat keep the disease at bay. Well,

other than cost a great deal too. The experimental medication boosted

my immune system and allowed it to perform much better. I haven't had

any kind of cold or flu over this time. Does anyone have any similar

experiences with LDN? If I've read correctly, I think I've understood

that LDN also boosts the immune system as well. I would welcome

other's with M.S., etc. who would like to talk about their situations

and compare notes from a patient perspective. I would welcome

physician input as well. Thanks for the time and God bless.

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