The Girl Who Cried Wolf - A Column by Kristi Page

happiness, love, Extraordinary doctors “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!

The Price of Being Completely Understood

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…

The Next Step in the Grieving Process: Healing

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,…

Lupus and the Beauty of Hindsight

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…

How I Explain Lupus Fatigue: Imagine Never-ending Jet Lag

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…

Wanting to Live Abroad, but Blocked by Lupus

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…

The Issues with Group Travel When You Have Lupus

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,…

Growing Old Before My Time

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,…