Danita LaShelle Jones,  —

Danita currently calls Madison, Alabama, home. She and her husband raise four exceptional children, one of which lives with hereditary angioedema — Ladybug. As a caregiver, Danita hopes that her column will show other caregivers and patients that they’re not alone. Championing the idea to “inform the world,” she seeks to reveal HAE in such a way that even if it’s rare for an individual to have it, it isn’t rare for everyone to know about it.

Articles by Danita LaShelle Jones

While it’s not the same, I appreciate your health anecdote

Usually, there’s screaming. Other times, there’s writhing and doubling over. But more often than not, there’s screaming. Every May around Mother’s Day, it’s easy to find a video where men, and occasionally young teenage girls, try a labor-pain simulator. Under normal circumstances, the simple contraption, a standard transcutaneous electrical…

Slowing down makes a big difference with HAE care

The entire day felt like a blur. Due to scheduling mishaps, a misunderstanding of departure time, and construction-related traffic delays, I had about 30 minutes to get from the airport entrance to the gate. Thankfully, I made the flight, and as the plane taxied down the runway, I concluded that…