The Burden of Feeling Like a Burden

When the doctor told me that I have lupus, I first thought only of the diagnosis. I had no clue that so much more would come with the knowledge that I would be fighting my body for the rest of my life. Guilt, depression, anxiety are just a few…

Staying Sane Through the Insanity

I sit here on day 11 of my first hospital stay of 2020. I’ve learned that pharmaceutical companies test how wide your esophagus will open to accommodate pills that would make a horse gag. I am doing all I can to remain sane, but few things make you lose track…

Tear Up the Contract and Communicate with Your Loved Ones

A lupus diagnosis affects more than just the patient. Spouses, children, close friends, and even co-workers are changed when a life-altering diagnosis is delivered. While the person with the disease has physical issues, their diagnosis has consequences for those around them. For example, a parent with small children won’t be…

Plagued by Anxiety: The Psychological Effects of Lupus

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,…

Do You Have Someone to Talk To?

Five years ago, when I realized my mother would pass because of lung cancer spreading throughout her body, one of the first things I did was look for a therapist. My mother was the first person truly close to me to pass away, and I knew it would…