Stem cell therapy with MS

[I_am_not_mafia]

I know some of you here have it, some good news: http://www.sth.nhs.uk/news/news?action=view&newsID=1035

Thanks for that. I wad diagnosed with it this time last year. It came out of the blue for me and within the space of a week I went from thinking that I was perfectly healthy to not being able to sign my name or use a knife and fork at the same time. Turns out that I had had some attacks previously but didn't realise because they were in silent areas of the brain. I will be very interested to see what my next brain scan reveals a year later.

I'm not on any medication for MS and am trying to control it by changing my diet and lifestyle. But it's good to know that this is showing itself to be quite useful. It amazes me though that people don't actually help themselves and just want to be cured without putting any work in. I stay away from all meat, dairy and cooked oils, avoid pro-inflammatory foods, make sure to regularly meditate, de-stress, eat healthily and get lots of sunshine. It makes me wonder how many people who get cured of their MS by rebooting their immune system will get it again as they revert back to their old lifestyles.