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I am a 54-year old woman with MS and Crohn's. I have been on Copaxone since

2000 after a few bad attacks. My last MRI showed no new lesions. I have been

taking LDN - 4.5 mgs. since June.

I did feel my right leg (the weaker one) start to feel stronger, but that is all

I can say positively about LDN.

My father passed away Nov. 5th after a brave fight with cancer. I really wanted

him to take LDN, but he was a real skeptic and when I arrived at the hospital

with my LDN, vitamins and all, I was told he could not take anything by mouth.

He was getting his nutrients by IV. I really wanted to help him, but could not.

Now, with the news about CCSVI, I have to see my neuro and tell her I want this

procedure and do it or refer me to someone who can do it.

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