Cindy has Alopecia Universalis. She lost all of her hair 62 years ago at a time hair loss was not talked about or understood! She endured a lot of teasing growing up, and that’s why sharing her story matters. Alopecia comes in many forms, and no one should feel alone in it 🩷 #fyp #alopecia | Georgia Hair Solutions & Salon
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Cindy has Alopecia Universalis. She lost all of her hair 62 years ago at …
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Meet Evie from the UK — a brave young girl living with alopecia universalis. Through the WBT Children program, we had the honor of gifting her a wig and giving her a moment she’ll never forget. The joy on her face says it all. This is why we do what we do — changing lives and building confidence, one beautiful girl at a time. #wigsbytiffani #wigsforchildren #wigsforkids #alopecia #alopeciauniversalis | Wigs By Tiffani
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Holly has Alopecia Universalis, an autoimmune condition which means she doesn't grow hair, including brows and lashes. Until Holly was in her 20s, her alopecia only affected the hair on her head. But, in her 20s, her brows and lashes decided to pack up and leave as well 😅 This led Holly on a search for the perfect brow solution. She began by drawing on her brows. Sounds simple, right? Wrong 😑 Drawing on brows was SUPER time-consuming each morning, and they never turned out how she wanted them.
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