Walking On Water - a Column by Shalana Jordan

“Go big or go home” has always been my philosophy. But I never planned on applying that motto to my health. One could say I definitely won the lottery no one wants to win when it comes to rare diseases and complications. To start, I’ve been living with lupus…

Facebook Memories is one of my favorite features on that social media platform. It reminds users of what they posted that day in years past. This week, I came across a Facebook Memory from two years ago that stirred up a lot of emotions. On Feb. 5, 2021, I was…

End-of-life preparation: What a bleak and unsettling subject. Will you be buried or cremated? Who will take your children if you die young? How will your assets be dispersed? I didn’t think I’d have these concerns at age 36, when I almost died. Death is inevitable, unfortunately, but most of…

Note: This column was updated Jan. 17, 2025, to correct that Soliris is an antibody therapy. Mental health is a topic that we’re starting to hear about almost daily in our society. It’s a subject that’s been taboo to speak about for too long. Finally, though, it is being…

Those of us living with a rare or chronic disease frequently talk about hospitalizations, medications, symptoms, fears, near-death experiences, and so much more. But something we don’t often talk about are finances. When the COVID-19 pandemic descended upon us, the International Labour Organization warned in April 2020 that nearly…

As my eyes slowly opened, I realized my vision was blurry. My head was throbbing, and I could taste blood. My right cheek felt itchy from the fibers pressed against it. But I could feel warm sunlight bathing my left cheek. I blinked hard to get my vision to clear…

Note: This column was updated Jan. 17, 2025, to correct that Soliris is an antibody therapy. Ding-ding, ding-ding. The ringing echoes throughout the unit, causing a brief silence. It sounds like the toll of a bell as a boat leaves the harbor. Then the unit erupts in unanimous…

It’s my favorite time of year: holiday season! That’s when we have Halloween, Thanksgiving, Christmas, New Year’s, and December birthdays for me and my kids. Having two autoimmune diseases and subsequent medical issues, however, makes it hard for me to participate in all holiday events. It’s easy to feel I’m…

Note: This column was updated Jan. 17, 2025, to correct that Soliris is an antibody therapy. I can’t think of a worse personal fear then having two autoimmune diseases during a pandemic. Every cough I hear in public sends me into a panic. I hold my breath while walking…

People die every day. Old age, illnesses, accidents — death is an inevitable part of life. So how is it that even when I was standing face to face with death, I still didn’t think for a second that I was dying? In September 2020, I almost died. I assumed…