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Hi Everyone,

I am new here and want to learn all I can. I have relapsing remitting

ms. An online friend of mine started ldn for her ms. She was very

impressed. I had heard about it a long time ago but kinda forgot about

it until she mentioned it.

I asked my neuro. for a script. Surprisingly she had no problem giving

it to me. She has another patient on it. She heads alot of ms studies

so I asked her why no one seemed to want to study ldn in a large scale

study. She told me the bottom line was money. That ldn had been

around a long time and had made it to the generic phase so there was

not alot of money to be made from it. I'm not sure how accurate that

is but it's sad to think, that something that could possible help

people, is being shoved aside due to profit.

I found a pharmacy that will compound the ldn. I am hoping it will

help. I went the copaxone and avonex route but had to stop due to side

effects.

Take Care

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