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Part 3: A Hair Loss Writer’s Experience Wearing a Hair System After this experience with nonsurgical hair systems, I learned that my (bald) head’s in a different place. In Parts 1 and 2 of this article, I spent time writing about how I felt, both physically and emotionally, wearing a hair system for five weeks. […]

Part 2: A Hair Loss Writer Wears Hair Systems and Writes My first question about hair systems was: “What’s that highlighter doing on my head?” As mentioned in Part 1 of this article, I recently spent five weeks wearing a hair system in order to better understand the experience of “wearing hair.” Earlier, I wrote […]

Part 1: My Experience Wearing Nonsurgical Hair Systems Wearing hair systems forced the question: What’s on my head versus what’s inside my head? What is it like to “wear hair”? I had never thought too much about this, but when it was proposed that I write on the subject, I was intrigued. I, myself, would […]

Trichotillomania Learning Center is an organization dedicated to helping and supporting those with trichtotillomania. Help, Support and Education for Those with Trichotillomania Trichotillomania (pronounced trik’oh-till’oh-may’nee-ah) is a disorder that causes people to pull out the hair from their scalp, eyelashes, eyebrows, pubic area, underarms, beard, chest, legs or other parts of the body, resulting in […]

NAAF Offers Hope and Support to Those with Alopecia Areata The National Alopecia Areata Foundation Tirelessly Pursues Its Mission Some 4.7 million Americans are afflicted with alopecia areata, an autoimmune skin disease in which people’s white blood cells begin attacking hair follicles, resulting in hair loss. Typically, alopecia areata presents with small, round, smooth patches […]