Hi everyone, I have been recently diagnosed with RRMS. I was directed to this website via my MS team and I'm really glad they recommend it. The doctors tell you what to expect with symptoms ect but they don't mention how lonely it can feel having a disease that not many people understand or can relate to. It's nice to know there are people who feel the same way I do and experience similar things because sometimes I feel like I'm making symptoms up in my head 😂 knowing I'm not is comforting! When I feel alone in this I can come to this website and be reminded I'm not alone and I'm not crazy 🤣