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Wow. . . full of energy!

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Hi Everyone,

I have SPMS since 1982, with the right diet, lots of excercise and a

positive outlook I have managed to stay out of a wheelchair. I'm so

greatful I finally found ldn. . . not allowing myself to give into

the " CRABS " I was on a lifetime search for something to stop the

progression, finally! I've been on ldn for about 2 weeks, I'm over

the leg stiffness and the sleepless nights, I'm really starting to

feel fantastic! My question is this, do I simply stay on the 3mg for

a while or do I venture out and increase my dose the next appt. with

my neuro?? Thanks for all your comments, it's really helped me stay

in touch with what to expect.

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