This post is inspired by Shift MS’ Youtube channel MS Reporters. MS reporters is a video library chock full of amazing content made by MSers for MSers, and I’m just loving this resource! They have a comprehensive video collection for people who are newly diagnosed where experts share three things every newly diagnosed MSer should know, and it got me thinking, what would be the 3 things I would say to someone newly diagnosed with MS? There were just so many things that came to mind, but when it came to narrowing it down to just 3 things I immediately focused on one of the hardest things I had to deal with: The emotions of being newly diagnosed.