When it came to my first six months with lupus, it felt like I took so many losses. My diet, my energy, my face, my body shape, the list just kept growing. I felt like I never got to take anything back. I never got to have a…
Columns
I write this in a state of disbelief and heartbroken shock. Not long ago I found out about the passing of someone whose presence merely graced my life, yet left a lasting imprint. I’d love to dedicate this column not only to one wonderful and strong woman,…
I recently was released from the hospital with more narcotics than a drug cartel, or at least that is what it felt like. Each one comes with its own issues and side effects. Instructions vary: Take after dinner,…
Though I openly hate it, I owe my good health to the prescription drug prednisolone. Anyone who has been prescribed the corticosteroid knows the love-hate relationship all too well. And while I can now look back and be grateful for its miracle powers of healing, there was…
Unbeknownst to me, there is a debate raging in online forums — and it has nothing to do with politics. The debate has been going strong for more than 30 years regarding whether birth control and hormone replacement therapy (HRT) causes flare-ups in Lupus patients. Most women are diagnosed…
As a lupus warrior, a hospital stay (or several) will be a definite part of the future. I am becoming an expert about making a hospital stay as pleasant as chronic pain will allow. Any hospital stay is a challenge for you and your whole family, especially if…
I remember the day I was diagnosed with lupus. And I remember the weeks that followed as I floated around in a haze of shock, not truly able to comprehend what was happening. I wasn’t in denial, but I hadn’t quite grasped what had occurred and…
I’ve always been a thankful person; expressing gratitude has never been an issue for me. When I was a child, my stepdad once told my mom that I was grateful even if I was given an empty paper bag. My gratitude caused my stepdad to do nice things…
There were times right after my lupus diagnosis when I longed for a relationship that was more than platonic. There were times when I felt I needed someone to hear out my frustrations and wrap their arms around me in a way that was different than a family…
There are situations where I know it would be beneficial for me to disclose that I’ve been diagnosed with lupus, but I just can’t. When it comes to my personal life, I’m all for being open and honest, even if it means stepping out of my comfort…
Recent Posts
- To my ‘forever nurse,’ who finally gave me my diagnosis of lupus
- New analyses show Benlysta may aid flare control, kidney health
- Can art therapy help lupus patients improve cognitive function?
- With chronic illness, checking in means asking, ‘How ya really doin’?’
- FDA approves Gazyva as lupus nephritis treatment