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.
When the doctor called and gave me the news of my diagnosis, I honestly felt that with a few meds, I’d be OK. As I look back on it now, I realize how ludicrous that idea is. I’ve always been independent and made my own way, and I was determined…
I pride myself on being a strong person. Over the years, however, my definition of strength has changed dramatically. When I was growing up in Chicago’s inner city, being strong meant never outwardly showing any fear. I’d fight for the smallest victories to let people know I was not to…
I think that whenever someone gets a life-changing medical diagnosis, their attitude is, “I’m going to beat it.” I could be wrong, but all the movies I’ve watched back me up (because movies are real), and this was the attitude I had. I felt sincere optimism that the medications would…
Learning a new skill is not easy. But you have an incentive to practice if it’s something you enjoy or find to be beneficial. I’m working on coping with my depression. I’ve discovered that if I want to be mentally well, I must learn how to handle this new lupus…
At one point when I was growing up, church was a fact of life. I learned that people tend to look to spiritual things more when life becomes difficult, or as I like to say, when we are tried in the fire. For most of my life, however, I…
I was a workaholic; I don’t have a hard time admitting that. Part of me was proud of my work ethic — after all, I was dubbed “Hurricane” because I worked circles around everyone else. Now I have lupus, and fatigue is a big part of battling this…
Living abroad was something I always wanted to do. When you move abroad, it seems people are a bit fascinated with you, and when you move abroad with health challenges, that heightens the fascination. Getting lupus made me witness firsthand what healthcare was like in the United States, and I…
I think that every time I’ve shared an article lately, I’ve talked about symptoms of lupus related to mental health. While I don’t particularly care for the pain, the fatigue, or the physical afflictions of lupus, the things that have caught my attention lately are more psychological. Several months ago,…
Many of us are frequently told, “You don’t look sick.” We can find that comment a little off-putting. While we recognize that it’s someone’s way of saying that we look “good” or “well,” that’s not how we feel about it. Not looking sick allows us to remain camouflaged among…
Many of us grew up with nicknames. Later, working in the real estate industry, it was common for people to adopt nicknames that helped promote their businesses. Because I never stopped working, one day my broker called me a “Hurricane in Heels,” and from that day forward, in the office…