Answers, Part II

It has been three years since I was diagnosed with Multiple Sclerosis. In the beginning, people and articles said, “Things would make more sense soon.” This filled me with more anxiety. What “things”? When was “soon”? It seemed to be a riddled threat, one I could not figure out… until now. I realize I was looking at it all wrong. The articles and people meant things — the ticking time bomb — had already gone off and that I would get answers as to why soon, now.

Back to Reality

It’s strange because sometimes when I talk about MS in person, I feel furthest from people. Yet, here — with the light of my computer screen — I feel like I have someone with me. I’m not judged. I’m not told I’m wrong or right… or how I should act or what to think. I’m not told anything. I’m just given a space. A space to think. And I believe when one can delve into their own thoughts — be allowed to fully think — that person is never alone.


I took to the internet for the first time to research multiple sclerosis. So it is here, on my blog, I have a stress reliever, a different form of a scrapbook, a way to record major information (mainly MS details). I also truly want to share my research with someone newly diagnosed… or someone who knows a person newly diagnosed. Information can be overwhelming, but hopefully, it will be more brief and not as scary here.