As part of our occasional “Dear Carolyn” series of personal patient perspectives shared by my readers, today I’m introducing you to Canadian heart patient, Linda Vardy, a retired high school math teacher. You might expect that Linda’s experience of undergoing triple bypass surgery at age 61 (after being told for almost a year that all of her cardiac test results were “inconclusive”) would be a dominant theme in her story – but that part is for a future post.
Here at Heart SistersWorld Headquarters, I’m often contacted by readers with impertinent questions like: “Why don’t you ever write about ______?” (insert your own specific diagnosis here). One in particular was a 2015 reader question that read: “Why don’t you ever write about congenital heart defects?” On that particular morning, I was feeling tired, sick and “grumpy” (as our little Everly Rose calls every feeling she has that’s not happy). I wanted to snap back at this reader that I’m not running the Encyclopedia Britannica here. . .
But in a remarkable coincidence – and luckily before I had a chance to snap – on that very day, another reader named Aletha happened to share with me her own amazing story as an adult living with a heart condition she’d had since birth. That weekend, I ran my first ever blog post about this cardiac condition, called “When babies with congenital heart defects grow up“.