Kellie McRae,  —

Kellie is a lupus warrior who spends her time teaching many about the incurable disease she battles with a smile on her face. She travels the world, writes articles, has an active YouTube channel and creates coloring and activity books for both adults and children. She is known as Queen Bubbly Bee because no matter what is going on with her body, she always manages to find the silver lining.

Articles by Kellie McRae

Losing It All, but Fighting Back

I opened my eyes this morning and knew it would be a great day to write. Why? Because with what I was feeling, I would be in bed all day. Pretty much everything hurts except my fluttering eyelids. Yep, no pain there. Battling lupus is like fighting the…

Trying a New Way

I think that because those of us battling lupus don’t look sick, people have no idea how much the disease affects every aspect of our lives. I know I’ve shared my feelings on this subject at various times in this column. Unfortunately, when your entire life is disrupted, it’s…

What Are Your Goals?

I have been asked what my goals are twice in the past two months. At one time, I would have told you that I was an ambitious overachiever. Now, I strive to get out of bed before 9 a.m. The first time it was on a questionnaire at the…

About That Greener Grass

Going to a hated job is something so many people complain about. They don’t like their co-workers, and if you could give them a two-hour lunch and a nap in the middle of the day, they’d be in line to sign up. Once upon a time, I would…

Keeping the Joy in the Midst of the Storm

Earlier this year, I shared in a column that I am chasing remission, and that lupus has caused a shift in my spiritual beliefs. Today I find myself revisiting both of these subjects. Have you ever had an enemy who said you couldn’t do something, and it made…

The ‘Normal Day’ Hangover

If you’ve ever partied like a rockstar, then you’ll know that while the night feels like it’s worth it, the next morning leaves you vowing never to party like that again. The night of a party is how it feels to have a high-energy, low-pain day with lupus.