How schools (too often) need to be educated about HAE
“Mom?” my oldest son’s raspy and weak voice said over the phone. “Can you come pick me up? I don’t feel good.” I had my keys in my hand before he finished the sentence.
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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