About Alopecia by Jeffrey Paul

This board is a news and information resource curated by Jeffrey Paul for anyone experiencing the effects of Alopecia. #HairLoss #HairRestorating
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FUNDRAISER: Tom Halliday.16, and his mum Sally of Hook are raising money for Alopecia UK. Picture: Tony Saxton
Alopecia World
AlopeciaWorld.com, ALOPECIA WORLD is a unique, exciting, interactive and positively life-changing social networking site for alopecians, their loved ones and friends.
Supermarket says sorry to alopecia sufferer Gail Porter after sending former Top of the Pops host promotions for hair products
Supermarket says sorry to alopecia sufferer Gail Porter after sending former Top of the Pops host promotions for hair products
Wigs for Kids - How our organization is changing lives - Jeffrey Paul's Hair & Scalp Specialists
This week, I want to spotlight an organization that’s very close to my heart. Wigs for Kids is a nonprofit organization that I started over 30 years ago when my beautiful niece came to me and told me that she would be losing her hair due to Leukemia. My niece, Laura, is no longer with us, but her legacy lives on every day when donors from all over the country cut off their pony-tails and donate them to children in need through our nonprofit organization.
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What to Expect from Alopecia Areata | Kayla Martell
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What to Expect from Alopecia Areata | Kayla Martell
Confident, happy and now wig free: My life as a bald woman
Sarah Peters has Alopecia and wants to talk to other women who suffer from it to tell their stories in a dramatic play. Photo Nev Madsen / The Chronicle
Alopecia Areata: Bald and Beautiful - Walker Tape®
Georgia Van Cuylenburg used to be a hair model in Australia. She suddenly lost all of her hair, and was diagnosed with alopecia areata. She made this great documentary that I think everyone should watch. It’s full of information and very heartfelt!
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Md. woman plans ‘No Hair, Don’t Care’ fundraiser for alopecia FREDERICK, Md. — Kayla Campbell turned a loss into a gain after her hair fell out. It took several years to get past the discouraging disappearance of her thick, wavy brown locks.
Life with Alopecia...Jaleigh's story
Jaleigh Murphy is like any other eight-year old in the second grade. She loves to sing, cheer, dance and play ball. She loves clothes, especially clothes that sparkle. But unlike most eight-year-olds, Jaleighs daily wardrobe is not complete until she puts on her wig -- or more often these days, a hat.