Alopecia World

www.alopeciaworld.com

Milena's Likes

March 2018

My Journey

I been diagnosed with Alopecia universalis since 17 years old, I am 25 now and I am still the same. This year is my first year I am barley starting to feel a little more comfortable with telling…

Blog My Journey 1 Like

January 2014

I feel so ashamed This is what happened: I'm in my first year of university and have met amazing people. However, one of my best friends of 6 years revealed me her secret and it absolutely shocked me. I never knew it… Discussion I feel so ashamed 16 Likes Finding love or just how to go about meeting… I have come out of a long relationship and now realize I have no clue how to get back into the dating world! I have so many questions. 1. When do you tell someone your wearing a wig? 2. Is it an issu… Discussion Finding love or just how to go about meeting… 4 Likes A special message just for you

I would like to express my sincere gratitude and wish you a happy new year. There is no way Alopecia World could be what it has become without input from individuals like you. The support, caring,…

Blog A special message just for you 13 Likes

December 2013

Science fair and alopecia

Hello,

My name is Devyn Napier and I am a senior in high school. I am extremely interested in the medical field and I attend an all academy school in Concord, Ca. I am in the Medical and…

Blog Science fair and alopecia 5 Likes

Welcome to
Alopecia World

Sign Up
or Sign In

Disclaimer

Any mention of products and services on Alopecia World is for informational purposes only; it does not imply a recommendation or endorsement by Alopecia World. Nor should any statement or representation on this site be construed as professional, medical or expert advice, or as pre-screened or endorsed by Alopecia World. Alopecia World is not responsible or liable for any of the views, opinions or conduct, online or offline, of any user or member of Alopecia World.

Badges | Report an Issue | Terms of Service