Welcome to Diary of a Tired Girl: Twitter edition! 🦋 I’m Charlotte and I blog about my life with ME/CFS. It’s not as depressing as it sounds, I promise! #blog
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Wearing a mask is a show of human kindness. If you can’t do it for yourself, do it for all the people you may be unknowingly infecting when you aren’t wearing a mask.
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It’s been almost a month since I posted this, and the fight is not nearly over. Here are some resources to help the BLM movement. 🖤
#BlackLivesMatter
It’s not over because your Instagram feed went back to “normal”.
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@DisabledDad3 @TN_Hope_D You have to find the right people to support you, and ignore the rest! I know that’s easier said than done but you can do it! You’ll know who the “right people” are, and you’ll never look back! ☺️
💛It’s results day💛
This morning I was awake super early, unable to sleep through the anxiety of results day. It’s true that second year wasn’t exactly what I imagined it would be, to put it lightly. Between managing my ME, many weeks of...
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#resultsday