I was diagnosed with RRMS October 2020 after I had optic neuritis. It appears that my first realapse was 18 years prior to diagnosis where I lost use of my right side but nothing else until last year which then lead to diagnosis. When diagnosed my neurologist advised that I was in the mild scale and did discuss DMT of plegridy or brabio but agreed it was sensible to wait a year until next scan and review if there was any change as I didn't feel it necessary to start treatment straight away due to low activity in symptoms. I have now had my scan and great news no new activity or symptoms therefore I thought it would be carry on as is for another year or until something happens, however spoken with my neurologist and his view seems to have changed to say I'm now mild to moderate leaning more to moderate but says I'm in a grey zone and it's difficult to advise if I should now be starting DMT I need to decide whats right for me but he has now suggested Tecfidera as a option which seems to have more side effects then what they originally offered I'm so confused do I start a treatment or leave it again? Also I thought I would have an annual MRI to monitor activity but the neurologist has said they don't do this, now I've had a scan after inital diagnosis scans will only be done if a major change occurs or relapse is this normal practice? I'm reaching out to my MS nurse but thought I'd ask for you comments too, thanks.