Columns

Put a Little Boogie in It

I find it interesting what some folks do to alleviate stress, to decompress and have a little fun, things sometimes I only wish I had the patience for. Adult coloring is one of those things that comes to mind. I have seen some really beautiful creations and a…

Complications Due To…

Almost daily there is a report inside one of my support groups that someone has received their butterfly wings – a term I use when someone has passed away from lupus. This happens more often than I would like to discuss. I am often bothered that their deaths are…

Living for the Little Things

My later years of high school were all about goal-setting. What did I want in the next six months? What about in the long-term? As an intensely goal-driven individual, I’d become accustomed to moving from one goal to the next with ease. With lupus, goal-setting is not quite…

The Battle with Brain Fog

I made my living for almost 20 years in real estate, and the funny thing that set me apart was the ability to remember things that others could not. If you told me your name six months ago, I would remember it six months later. Lupus does…

Weathering the Storm

One thing that affects my illnesses profoundly is the weather. As temperatures have started to drop, my body already is feeling it. So, I only can imagine what anyone feels like who has survived the recent onslaught of severe weather that has impacted our country — especially those with chronic…

The Psychological Impact of Lupus

Do you have someone in your life who doesn’t understand why you are always “sick and tired?” Is it hard for them to fathom that the illness you have won’t go away after a good nap or latest diet fad? And are they confused as to why you may…

Still Waiting to Pay Bills? Consider Work Options

I saw a statistic that said that only 31 percent of adults with lupus are working full time. The rest of us are just battling it out. If you are like me, you applied for disability, but with the backlog or whatever reasons they have for not getting…

How My Positivity Has Masked the Severity of My Illness

Last week, Selena Gomez posted a photo on Instagram about her recent kidney transplant. Her openness about both her condition and the treatment has undoubtedly been a much-needed catalyst to greater awareness and recognition of lupus, especially since her latest surgery. As part of our ongoing ritual…

We Can’t Do It All

Battling lupus stinks. It takes so much out of you. When I was diagnosed, I was selling homes, I had a full social life, and I was a big ball of energy. I would cook, clean, entertain, and work. As lupus settled into my body, I have…