The Words We Use

I’ve been trying to write this post for a couple of weeks. My thoughts and feelings balked at being committed to paper. I think I’ve worked through it enough to write now, so we’ll see… First, I read an article on Migraine.com (https://migraine.com/expert/fighting-for-migraine-with-words/) by Dr. William B. Young about how the words we use affect …
Continue reading The Words We Use

Keepin’ on keepin’ on

It’s been a while since I posted. #gradSchoolSucks and all that. I have been struggling with a lot of stuff this month. The “on this day” feature of Facebook has made it clear that October is migraine month for me, and this month was no exception. In fact, my migraine monster decided to go for …
Continue reading Keepin’ on keepin’ on

Do the Cha-Cha

It seems like every time I think I’m starting to make real forward progress, something sets me back. I mentioned a few weeks ago that I was pretty sure my rheumatoid disease was not, in fact, in remission as Dr. B seemed to think.  My joint pain had been steadily escalating since spring, with some …
Continue reading Do the Cha-Cha

Spoonie product review – Pill Suite

I hadn’t reviewed the Pill Suite yet because I’d had issues with the bags.  I have since gotten replacements and am now THRILLED with this solution for my meds and want to share. As most Spoonies, I have a LOT of medications/supplements I take multiple times a day.  I have struggled with the standard pill …
Continue reading Spoonie product review – Pill Suite

On becoming a spoonie

 Christine Miserandino penned a story about how she shared with a friend what living with Lupus was like.  (http://www.butyoudontlooksick.com/articles/written-by-christine/the-spoon-theory/)  This metaphor gives language to the struggles people who live with chronic illness face, and a community of “spoonies” has arisen.  I joined the ranks of spoonies last year, and everything about my life has changed. …
Continue reading On becoming a spoonie