10/19/10
Update: October 2010
There's very little to report....it's been over 7 years since I was diagnosed with MS and I'm still doing great. And I'm still taking LDN and nothing else for my MS. I have no interest in trying anything else because this is working so well for me; no major relapses, no new symptoms, nothing ever since I started taking it. I do try to spread the word on this amazing treatment whenever I can, but it's not like I'm around a lot of MS patients. Actually, I don't even know any MS patients anymore and haven't visited any MS websites for years. I do have MS but I don't do MS....it's a boring topic. I wish people luck if they have it, but so far it hasn't affected me that much....so far...
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awesome website. just started ldn very inpressed. went on about a week ago. 1st night i felt my feet for the 1st time in about 5 years or so. No numbing feeling in them. can't fait for brain fog to finally lift and have some spacisity. which is common from the reading I have done. I can't believe the doctors who say they have not heard or don't know what it is. Look at all the people they have sworn to help and have not. The people who are crippled, whose lives have been ruined. I do not understand. Well actually like our government, all about the money. Thanks for your writing.
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