“Kristi” is a surfer, barista, and university student studying for arts and science degrees in philosophy and mathematical modeling. Living on the picturesque Bellarine Peninsula on the southeast coast of Australia, she’s deeply passionate about salt water and amazing coffee — even though she’s not allowed to drink it. Above all else, she loves traveling the world! Diagnosed with stage IV lupus nephritis at 20, she’s determined to not be defined by her autoimmune condition. Using writing as a medium for self-expression, she hopes to share her life and journey to both raise awareness and support others in similar situations. A big believer in the concept of dialectics, she loves sharing and hearing unorthodox, sometimes controversial, views. She’s quirky by choice, inquisitive by nature, and smiling always!
As humans we long to have someone relate to what we’re going through, to be accepted and understood. For a very long time I didn’t have to work very hard to achieve this feeling. Nowadays, it’s something I want desperately, but I know that to have it…
My diagnosis of lupus was a lot of things. It was a shock to the entire system. It was an introduction to a new world that was completely unknown to me. It was the catalyst to the greatest internal struggle I’ve ever experienced. But more than anything else,…
Though it took me some time to realize, there were certain things that I lost in the instant I was diagnosed with lupus. The saying goes that we never know what we have until it’s gone, and for me that couldn’t be truer. There’s a whole other…
With three daughters to raise, my parents always worked hard to promote positive body and self-images within our family unit. Ever since I can remember, my mum has tirelessly emphasized that we should accept our bodies as we are, ingraining within us a sense of confidence and…
If you’ve traveled far from home, it’s likely you’ve felt jet lag. There’s nothing quite like the euphoria of knowing you’ve got nothing but work-free, relaxing days ahead of you. But there’s also no other phenomenon like jet lag ― unless you live with lupus fatigue. When I…
I’ve spent my entire life struggling to consolidate my feelings toward religion. And, while facing an adversity like chronic illness often leads many to turn to one deity or another, this wasn’t the case for me. I’d like to preface this column by clarifying that I have…
As I sit writing this in a small pub in Edinburgh, Scotland, I’m both elated and disheartened. In the last 28 days, I’ve traveled in 10 countries throughout Europe, falling more and more in love with each destination I discover. My love for the world has swelled…
Being diagnosed with lupus has taught me a lot, not only about myself but also about my self-worth. Sometimes I used to find myself a bit disheartened when I thought not just about relationships and love but also friendships, worrying too often that because of my chronic illness…
Late last year, I booked a 16-day Contiki tour in Europe with my sister. Group travel is awesome because there are significant discounts when you travel in a group of 50. Plus, it is a once-in-a-lifetime experience to make amazing new friends while exploring the world. But,…
Every time I go for an appointment with my renal doctor, I’m reminded that I’m an anomaly. Before seeing my specialist, I jump on the scales in the waiting room, the procedure for all patients. But as I unlace my shoes and step up to be weighed,…