Meghan Bea

That first doctor’s appointment with a new rheumatologist can be stressful, no matter how long you’ve lived with lupus. You might be a veteran lupus warrior who is switching doctors...

One of the hardest parts of being diagnosed with an invisible chronic illness like lupus, is that your friends and family might not understand your illness. Often, they might say...

Since becoming sick with lupus, I travel far less than I used to because the act of traveling is difficult due to the fatigue I live with everyday. Thirteen years...

As soon as I graduated from college and moved into my own place, I knew I wanted a furry friend to share it with. I’d grown up with dogs and...

Like most lupus patients, I always wonder if I’d be treated differently by my family, friends, and doctors if my illness was visible. If I used a wheelchair, would people...

In my work as a violin teacher, I come into contact with dozens of students each day. Unfortunately, this also means that I’m exposed to dozens of students’ germs each...

Ask most lupus patients and they’ll tell you that their symptoms are worse at a particular time of day. Many patients feel increased fatigue or joint pain at the end...

Life with lupus can be unpredictable, inconvenient, and exhausting. Because I live with daily chronic fatigue, everyday tasks that are easy for other people are not so easy for me...

I hadn’t experienced sensitivity to ultraviolet (UV) rays until this year, despite living with lupus for the past thirteen years. I’ve learned that lupus symptoms can change and evolve over...

Many new patients with autoimmune diseases, particularly young women, are dismissed, not taken seriously, or even gaslit by doctors. During the year I spent searching for a lupus diagnosis, I...

I'm not alone in struggling with lupus insomnia. Insomnia can majorly impact patients’ quality of life, especially since so many of us already live with chronic fatigue. In the months...

Since becoming sick with lupus, I've needed to sleep 2 to 3 hours more than my able-bodied peers in order to function. In addition to fatigue and skin rashes, lupus...

When I first became sick with lupus, I had no idea how much my life was about to change. I had to learn to carefully manage my energy, juggle doctors’...

During my first five years living with lupus, I used to wake up an hour early before work. Even though my fatigue was at its most severe in the mornings...

Brain fog: it's one of the most frustrating symptoms lupus patients have to live with. Brain fog sometimes feels just like its name suggests: a thick fog in your brain...

With its pumpkin patches, apple cider, and promise of comfortable weather, autumn is many people's favorite time of the year. The hint of crisp, cool air offers a reprieve from...

I’ve spent most of my life living in between the lines; I’m too sick to work a full-time job, but not sick enough to qualify for SSD (Social Security Disability)...

When I first became sick with lupus, my life changed overnight. Fatigue, pain, and endless doctors’ visits replaced school, my social life, and my plans and dreams for the future...

We celebrate birthdays, weddings, and baby showers with gifts. But why is it less common to give a gift to someone when they're going through a divorce, have lost a...

Traveling always triggers my chronic fatigue. The long wait at the airport, having to stand in line, and carrying a suitcase all zap my energy. At home, I can use...