Well, as most of you know, I was diagnosed with Multiple Sclerosis on December 2nd, 2018. I have so much to say about MS, and all that life with MS entails. I understand that constantly posting about it on social media is obnoxious, so I figured I would blog my story, my journey and everything in between for those who want to follow along. I know most of you have heard my story about diagnosis, but for those of you who haven't - here it is. On November 28, 2018, I woke up and had some minor numbness and tingling in my feet. As a mom, my first thought was, "Ain't nobody got time for that," so I brushed it off and figured I must be getting a virus of some sorts. On November 29th, the numbness and tingling had worsened and traveled up to my peri area. As a Registered Nurse, I figured I must have slipped something in my back while skiing the weekend before, so I made an appointment with my primary care office. I saw a covering doctor that visit. As a young, otherwise