Nicotinomide

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

If you type in nico in the search box 3 topics come up may help you.

Bertie

1 Like

Nothing came up

Not exactly the same, but when trying to give up smoking I used Nicorette mouth spray, and still use it now - I find it keeps pain to a minimum besides making me feel better.Consultant and GP know I use it, and nobody’s screamed about it yet…