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When you think of ultimate frustration you think of the phrase, “ripping my hair out.” However, there’s no need for me to do that because in the past few weeks it’s started to thin and fall out on its own. Earlier in the year, it felt like I…

I’ve been blessed with many supportive souls since my lupus diagnosis, a few of whom also live with chronic illness. One of them, along with her partner, has taught me a most valuable lesson, by being my constant reminder that sometimes it’s not about leaps and bounds, but…

You probably have heard the phrase “Sex, Drugs and Rock ‘n’ Roll.” I was used to hearing it as well as I grew up in the music industry in Los Angeles, with parents heavy into the ’80s rock scene. I grew up being told I was a rock star. No matter what…

Every Thursday, I get up early – a feat in itself – and drive half an hour to meet my personal trainer for a 45-minute pain-and-sweat session. While I love these mornings, they come at a cost. If I’ve made plans with someone later in the day, it…

Veganism is a popular topic of late and, while I have opinions, its nutritional merits are not what I want to write about. Rather, as someone who lives on a medical – read: necessary and involuntary – elimination diet, I wish to kindly ask the vegan community not…

When I started feeling bad and had no idea what was wrong with me, I thought I could go to the doctor and they would figure it out. There would be a shot or a pill and all would be fine. Life would return to normal. Fast-forward months later…

While my disease is doing better each day and I am feeling better with every treatment, there are some things that will never go away. I will never be “cured” in the traditional sense. I’ve tried so many things and so many doctors, and have been poked and…

Being diagnosed, I felt like the weight of the world got lifted off me. But slowly, as I began to understand more and more, I started to feel something else. I felt heavy and hopeless with my new lack of possibilities in life. Over the last month or…