Hello! I was diagnosed with RRMS in 2011. At that point that’s when the world stopped. I didn’t even cry I just sat there for hours just taking it in. I’ve been on every medication known to man and as I got older it started to progress. I was on Tysabri for a long while! Now I’m on Ocravus PPMS is horrible and I’m numb in a lot of areas. Basically MS can kiss it!!! But I try to stay as positive as humanly possible because I can’t live the rest of my life mourning a disease I have no control of. So I try to eat healthy, exercise and keep my mind busy! But even then it’s hard! So, yea. That’s just a little preview of the life of me! Hope all is well with everyone! Please take care of towels and NEVER give up! It’s not an option!