Hi All,
I’ve not been on here in a while, but where do you go when looking for info/advice!
Some years ago someone on here gave lots of Info about the benefit of nicotinomide in MS, it was compelling and I started taking it with good results. For some reason, which I don’t remember, I stopped it, I think it may have been that I could no longer get it, don’t know!!
I see it is now readily available, does anyone have and info on it or take it themselves? I’m wondering about what dose to take read somewhere 250mg x 2 daily but the tablets seem to be 500mg and x1 daily.
Any info gratefully received.
Sue