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I'm another " newbie " . . . Have been taking ldn for MS for about a

week. I've had MS for over 20 yrs, I've been a real rebel when it

comes to the ABCR injectables. I'm proud to say I've been doing

very well with my disease. Let me ask everyone an obvious

question. I'm experiencing some of the common side effects of ldn,

(I take 3.0 every night around 9:00pm) leg stiffness and trouble

getting back to sleep when getting to use the bathroom (usually

once). I have noticed a lot more energy throughout the day, wish

really excites me. I want to thank everyone for their helpful

comments. It's a shame more people aren't aware of ldn, I try to

tell as many as possible. Until the next time. I look forward to

your comments.

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