Hi, I’m Meg, and I have a rare disease called Spinocerebellar Ataxia – Type 1. I used to be a high school English teacher, but now I’m a stay-at-home mom who’s sharing this next chapter of my life (& attempting to promote SCA awareness) through this blog.
Having been stuck inside for nearly five months, I’d sure love to go on vacation. Unfortunately, our country’s handling of COVID has put a bit of a hiatus on anyone’s travel plans right now.
Continue reading “Revisiting “Return Here” Favorites: Road Trip #3.5″
Ah, the power of perception. How two people can read the same exact book (or, say, news article) and have very different interpretations of it. Interpretations that are worth explaining and learning from, even when you don’t agree with them.
The #BlackLivesMatter movement has RIGHTLY taken America – and other parts of the globe – by storm. Hopefully, its instant popularity directly leads to a large number of successes. And it should definitely be noted that one key aspect in how quickly and widely #BLM has spread is because of how inclusive it all really is.
I pride myself on being a pretty positive person (with a natural knack for alliteration). This blog gets compliments all the time on how it helps others be more optimistic.
Which is why Facebook is killing me.