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From the Archives: Three-and-a-Half
I was three-and-a-half when I knew something was different. I sat on the front porch, waiting for a car to pull up, wondering how long it would be until I got to the house where my grandparents lived. I crossed my legs at the ankles, trying not to wrinkle the dress I was wearing for that special occasion. It was pink and it was soft, the kind I liked, the kind that didn’t bunch up too much when I had to sit for long periods of time, and my dark brown hair was down, though my natural curl made it stick out in all directions. My baby sister Lindsay was…
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Hypochondriac
When I was a kid and somewhat sick from a cold or other bug, my dad would take a look at me and if I wasn’t actively throwing up or profusely sweating, he’d send me to school. I always hated it – why didn’t I get to stay home like every other kid? “You’ll live,” he often said when I whined about something that wasn’t life-threatening. That’s the thing about growing up with a parent who is a medical professional – you cannot be wimpy about illness. They’ve seen worse. I’m not sure I was a less-whiny kid about my minor illnesses, but as I grew up, I knew that…
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From the Archives: That’s What We Have Right Now. Hope.
My dad arrived a week before Christmas. Initially, when Shawn was diagnosed, he’d offered to come in January for the duration of the chemotherapy. Shawn and I thought it would take about six months, and my dad could help our family until the worst was over. What we didn’t know was that my dad had different plans. After he saw the scans that were taken a few days before Shawn’s colonoscopy, he knew it was much worse than we realized. I didn’t know till later that he’d sat at his computer in his living room and held a printout of the scan, crying as he looked at it. My dad…
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From the Archives: Marjorie, What If I’m Dying?
Throughout the past 4 1/2 years, I’ve written pieces that never appeared on the blog. Sometimes, these pieces of writing were too raw for me to share, and sometimes they were simply musings that I wasn’t sure were interesting for a bigger audience. Often, I wrote to process what had happened and to try and understand how my life had turned out the way it did. These writings went in a folder, and for the next few months, I plan to share some of them with you. I’m calling these posts, “From the Archives”. Here’s the first one. The pain in Shawn’s gut became obvious at the end of October,…
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Widows in Quarantine
I’ve taken Covid tests so often that I know what to expect. There’s always a bit of fear, but then…everything is fine. I’m tested every week at school, and I’ve taken more rapid tests than I can count. We made everyone Covid test for our wedding. And every single time I’ve taken one, it’s been negative. Apparently, according to my dad and the National Institutes of Health, having an allergy to nuts (which I have) lowers your risk of getting Covid. Hey, I’ll take it! I mean, I’m a teacher and have been teaching in person for over a year. I have three kids in different schools and I eat…
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National Colorectal Cancer Awareness Month
It’s only been a couple of decades since President Clinton declared that March would be National Colorectal Cancer Awareness Month. And it’s only been a couple of years since I’ve known about it. It’s strange, how unaware I was about colon cancer, an illness that is the third most commonly diagnosed cancer and the second leading cause of cancer death (in men and women combined) in the United States. Seriously, before Shawn got colon cancer, I’m not sure I knew anything about it. It was a disease old people got, right? That’s why you got a colonoscopy when you’re old, right? I guess it could seem surprising that even though…