I just wondered if anyone could give me advice please. I was diagnosed with RRMS in May 2016 and been using Copaxone ever since. I’ve had about 5 MRI’s since and on every one there have been new lesions which are active so they are looking to change DMD and suggested I try Tecfidera to see if that slows down the progression before I try Lentrada or similar. Now I know everyone is different but it really worry’s me that it has ‘progressed’ this quickly. I know Copaxone is the ‘weaker’ DMD but I did think it would be a while before I needed to change. Has anyone else had this experience?