In other news: On Botox, Thailand, and ALS

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In other news: On Botox, Thailand, and ALS

In the first post I published here after returning from summer break, I shared a recap of some of the bigger changes that took place while I was away from the blog.

I didn’t tell you everything, though. A couple happenings just didn’t seem to fit in the bits I previously passed along. Those being the following…

BOTOX

I got Botox shots in June! In my …

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Summer break ends: What changed while I was away

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Summer break ends: What changed while I was away

Grandma’s Briefs is back! Yep, the summer break I announced at the start of June is officially over.

While I was away from the site, a few changes took place. Some big, some small. Here’s a (relatively) quick update:

For starters, one blog change is that Grandma’s Briefs hit the 10-year mark in July! Hard to believe but true, as you can see from my very first post, published a decade ago.

Another blog change is that you’ll see a few new faces in the Meet the Family section of the sidebar, those being of Andrea’s new …

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Multiple Sclerosis Awareness Month: My MS and me

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Multiple Sclerosis Awareness Month: My MS and me

March is Multiple Sclerosis Awareness Month. Though I have MS, I don’t write much about it because, frankly, it’s long been just part of who I am, not what defines me. There are far more informative bloggers when it comes to all things MS—my dear friend Cathy of An Empowered Spirit foremost in my mind—so I typically stick with grandma-focused sorts of stuff.

Yet, with MS becoming a bigger (sometimes overwhelmingly so) focus of my life in the time since last year’s MS Awareness Month, I figured I’d spend at least one post sharing the relatively recent changes to my MS and me. Perhaps doing so will put…

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MS and must-see brain matters

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MS and must-see brain matters

As many of you know, I have multiple sclerosis, having been diagnosed with relapsing-remitting MS in 1992. I've done fairly well with the condition over the past 26 years, with the help of progressively stronger drugs along the way. In fact, most strangers—and even some folks I do know in person—have no idea I have MS because, for the most part, it doesn't show. It's one of those "invisible" diseases.

As such things go over the years, though, some of the effects are becoming less invisible. Especially to me. Especially those darn…

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