It’s never the energy boost, it’s always the lack of and when you try to explain it to someone who doesn’t understand you know it’s a waste of time. Platforms like this mean so much because when you say the magic word, other MSers just know. It’s like a curse word. Today was a heavier fatigue day and I’m not sure why. The headache was stronger. The dizziness was as fiercer. It’s like these symptoms are just becoming worse, but like any other day, we push through. That’s the thing about an MSer… we never backdown from the fight and we never walk away from the chaos. There’s always been that part of us that was meant to make the storm shake in fear. I say all of that to say, I see you too through your fight and I stand with you through yours. Tomorrow we fight, dizzy, in pain, symptoms or not…but together all the same. Each one of us are suffering in a different way because this disease strikes a different nerve, and we’re uniquely beautiful beings.. just glistening snowflakes. ❄️❄️❄️❄️❄️