Questions heart patients should ask before getting an MRI scan

by Carolyn Thomas   ❤️   Heart Sisters (on Blue Sky)

Since I was diagnosed with breast cancer in April, I’ve become obsessed with my hospital’s diagnostic imaging procedures – so far, that list includes my mammogram, ultrasound, MRI, CT scan, bone scan, heart scan (MUGA) – and of course (although not a scan) – my all-important Core Biopsy procedure at the Breast Imaging Clinic.  Keeping track of appointment instructions – plus drinking water non-stop to flush stuff like contrast dye out of my kidneys – are now my full-time (unpaid) jobs.  You can read more about my breast cancer experiences so far in these posts
Continue reading “Questions heart patients should ask before getting an MRI scan”

Dear Carolyn: “After 19 months of daily discomfort, my pacemaker was replaced”

by Carolyn Thomas   ♥  @HeartSisters

             .     Clayton & Linda Vardy

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.

Ten years after her surgery, Linda was told that she now needed a pacemaker implanted. And that’s when things started going sideways. While I was reading her story, I couldn’t help wondering if Linda might have been treated differently had she been a male heart patient.  Read her story and let me know what you think. . .       . Continue reading “Dear Carolyn: “After 19 months of daily discomfort, my pacemaker was replaced””

Hello pacers! A little Q&A about your pacemaker

by Carolyn Thomas    @HeartSisters

Here at Heart Sisters World 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“. 

And recently, a similar reader contact reminded me that I’ve never covered the topic of cardiac pacemakers – until now. Continue reading “Hello pacers! A little Q&A about your pacemaker”