Of all the places to have a meltdown, mine happened in the parking lot of the public library. Last summer, my daughter, whom we affectionately call Ladybug, was hospitalized several times overnight due to hereditary angioedema (HAE). When she was at home, I had to administer multiple IV sticks…
From the Caregiver's HAErt — 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.
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