A few months after I was made unrecognizeable and deformed by an unethical, greedy fame hungry plastic surgeon, Richard Ellenbogen (He removed all the internal anatomy from the tip of my nose and a good ways up my bridge) -- I got MS. I was in so much emotional pain and humilation from going from being a model to looking hideous and deformed, and my body went into shock -- I got paralysis on the left side of my body and my entire midsection also went completely numb.

Because I lost my ability to walk, I was ordered to take an MRI, and I was diagnosed with 3 new lesions and no old lesions. I was informed that I just got MS. I read that MS can come out of nowhere and often happens to people who lose their kids or have something extremely horrible happen to them. It often shows up in times of the most extreme stress.

Anyway, I was put on avonex. Shortly after taking avonex, I read about LDN, and how it halts the progression of MS. However, I could not find a doctor to prescribe me this oral medication that cost only about $5/month. So, I had to take an injectable medication -- where the needle is super long, and the medicine costs $1,500 per month! My numbness and paralysis did not get any better with the avonex or the steriod therapy -- Solumedrol. Plus, I felt very sick and very tired from these medications.

Finally, I found a doctor who prescribed me LDN after having been numb and paralysed for about 3 months. Within 3 days of taking the LDN, I could feel my midsection again. My foot and part of my leg are still numb, but I have to say with the LDN, I got about a 70% improvement and no worse symptoms since I got diagnosed with MS 8 months ago.

So, if you or someone you know suffers from MS, I suggest looking into LDN. Another thing I sugges is that all people with MS get tested for Lyme disease because a lot of people get misdiagnosed. Lyme disease is treatable with antibiotics.