And so we head back east from Seattle for the final week of our final cross-country road trip (for now)…
Continue reading “Across America Again: Road Trip #3, Part II”
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.
And so we head back east from Seattle for the final week of our final cross-country road trip (for now)…
Continue reading “Across America Again: Road Trip #3, Part II” →
My last post has me fixated on planning our next road trip. But, since we’ve got a while until that takes place, allow me to reminisce as I take you through our last cross-country adventure for now!
Having taken a brief summer vacation to Maine, we only had one corner of the U.S. left. So, in 2018, we set off from good old Western New York to Seattle, Washington.
Continue reading “Across America Again: Road Trip #3, Part I” →
In one of my first posts, I made a point to say, “I have Ataxia. Ataxia doesn’t have me.” Separating yourself from your disease is an essential part to being able to stay sane and happy. If you have a chronic illness, it’s so important not to let it control your life. So important, yet so difficult.
Continue reading “The Unnecessary Effect of Ataxia Anxiety” →
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About a month ago, really just as a means of coping with my resignation, I published my “Top Teaching Tips” … a post that got more views, shares, and comments than anything else on this blog. Its instant popularity was entirely unexpected and completely floored me.
Continue reading “Teaching Vocabulary in the Least Painful Way Possible” →