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RE: New diagnosed ms patient

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Hi

All the people in this group (5,000??) are taking LDN - I would say about three quarters of them have MS and I presume that all of them benefit from taking it since they are still doing it! My husband got diagnosed with MS about 7 years ago - he never took any of the recommended drugs as he works and couldnt (and wouldnt) feel sick for two days a week at such a huge financial cost.

I found LDn online like you did and he`s been on it for almost 6 years. he takes nothing else for his MS other than a handful of vitamins - he feels fine and still works every day. He has no new symptoms, no relapses, nothing. It appears to have halted the progression entirely. He has an annual MRI and no new lesions have appeared.

I think the other people that take LDN for MS will have similar stories - maybe some on it for even longer, some for less. Most people on it long term dont come here to post every day as they are getting on with their lives - I stay and offer support and tell our story as I like to pay it forward and belive that everyone should have a chance to learn about it and get on it!

So good luck with getting a script and hope your husband does well on it - get it compounded at a recommended pharmacy and hopefully his life will continue in good health.Bev

low dose naltrexone From: WDCIHC53@...Date: Thu, 24 Feb 2011 20:57:27 -0600Subject: [low dose naltrexone] New diagnosed ms patient

My husband was diagnosed with ms last November and since then has been taking rebif. We are looking for another answer because the rebif leaves him feeling like he has the flu. In researching ms, I ran across the Ldn website and we are very interested in finding out more about it. Does anyone have any input on how Ldn has helped them deal with their ms?Thanks,Sent from my iPad

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http://ldn.proboards.com/index.cgi?

>

>

> My husband was diagnosed with ms last November and since then has been taking

rebif. We are looking for another answer because the rebif leaves him feeling

like he has the flu. In researching ms, I ran across the Ldn website and we are

very interested in finding out more about it. Does anyone have any input on how

Ldn has helped them deal with their ms?

> Thanks,

>

> Sent from my iPad

>

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