Hi, my name is Tima. I was diagnosed in 2020 with RRMS, the beginning was hard and scary because it's something I didn't know or was aware of. I've gotten used to some things, but there are some things that are still hard to get used to. There are times when I feel out of place with things, but I do talk to my family about it which helps to talk about. I want to communicate and share my experiences with others who understand, and whom are going through similar situations or challenges.