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Hi everyone, my spouse has RRMS and has been relatively well since adopting the OMS lifestyle almost 6 months ago.

I have been following MS Hope and the Best Bet diet for a while now and I felt this video was worth sharing

https://www.youtube.com/watch?v=Jy4b6nnx5yA
Thanks for sharing.
I agree all that is said in this video.
One medication that isn't recommended by most neurologists is LDN which is what I'm on.
I chose it due to its lack of side effects and its ability to deal will my fatigue.
2 posts Page 1 of 1

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