Does anyone have a view on this treatment for RRMS. After reading the research clinical trial using 132 Pts- I am more inclined to try and push for this treatment when I meet my neurologist more than Lemtrada. Yes, some are of the view this is like using a sledge hammer to crack a nut- but I take a similar view to that of @tracey and what to have a big fight with MS. With that in mind and given my hospital in Sheffield is linked to this clinical trial I have completed pre trial screening questionnaires via Dr Burt in Chicago USA to see if I meet the inclusion criteria. I know in some cases it can be available on the NHS, but I get the impression 'I'm not bad enough, from the direct and indirect feedback I'm getting. You are experts in my eyes and just wondered if you would mind sharing any views on this. Thanks.