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!

Without A Safety Net, I Have Nothing to Lose by Trying

What would you do if you knew you couldn’t fail? I love this question because when I ask it, the face of my conversational partner lights up with excitement and confidence. And why wouldn’t it? I’ve given them the ultimate scenario, the prospect of theoretically being able to do anything.

A Life with Illness Is Worth Fighting For

You’d be surprised how many times I tell the story of my tumultuous diagnosis, only to have someone ask, “Then what happened?” It’s like they think I went to bed and accepted lupus as a death sentence. Don’t misunderstand me: Lupus is a killer. If left undiagnosed, it can be…

Life with Lupus Requires Resilience

If asked about the one thing that’s necessary when living with lupus, I’d answer “resilience” without skipping a beat. Strength, good doctors, a brave face, and a solid support system would be in the running for second. But in a life with chronic illness, resilience makes or breaks you.

Why I Can Only Discuss Hardship After the Fact

When I’m in the depths of struggle, only the people closest to me know about it. I need to go through the hardship and come out on the other side before I’m comfortable writing about it or sharing it on social media. I need to prove to myself I can…

Hindsight Provides Lessons for My Past Self

If you had the chance to sit down with yourself just after your diagnosis, what would you want to say? If you only had an hour, what wisdom would you impart? Would you warn of the grief and hardship ahead? Would you right the mistakes in your journey? Would…

With Lupus, Tired Is a Constant State of Being

It doesn’t matter how little I work or how much I might sleep, there is no way for my body to catch up with my fatigue. Sleeping for three hours or 14 hours makes no difference. I still wake up feeling as if I’m starting the day on the back foot.