Comment

Comment by T on April 23, 2012 at 2:54pm

If find now that when I made the decision to not wear wigs anymore, it has given me a freedom to speak out loud about Alopecia. I've met so many people that have come up to me asking about my shaved head. It's funny to me because where I live, few people smile at you, let alone talk to you. But since going bald, people smile at me (not laugh) and ask me questions, and I enjoy telling them what I have and how I've accepted it. So facinating! I like it. It has given me a confidence I've been lacking for a very long time.

Comment by Hannah Dennis on March 30, 2012 at 12:35pm

hi a little while after i was first diagnosed with alopecia i made a video for youtube and here to create awareness and general support for others going through the same :) even though i was still struggling to come to terms with it myself especially then when i had not yet shown anyone i knew until a year after becoming bald i found that making this and sharing my story with as many people as i can really helped me as well as others at the same time i just wish i could do more and hope that one day i will :) x please check it out xxxx
http://www.youtube.com/watch?v=8ld9wGSI8-c&feature=plcp&con...

Comment by PJ on September 19, 2011 at 12:11pm

Praise the Lord, for all that He is and will be doing with His children. Iron sharpens iron and He uses the most unvaluable person to do His works.

Comment by Jacqui on September 19, 2011 at 7:57am

I always love to encourage others with alopecia. I've been wearing my head bald for almost two decades. Most of that time, I did not wear a wig. Whenever I did wear a wig, I felt more uncomfortable than when I wore my head bald. In 1999, I was featured in an article by The Washington Post .http://wapo.st/qIdP4C I have never been upset about the hair lose, but always felt it made me uniquely me. After this article, I came to realize that there were/are so many who suffers in silence. I do feel that I have a responsibility to share with others in helping them embrace the baldness, whether or not they decide to wear or wig.

Comment by margaret watson on August 30, 2011 at 1:18pm

I use my difference by walking tall and going absolutely everywhere 'bald'. I can honestly say that now (being bald totally for past 3 years) I am unaware most of the time and never get comments or strange looks from adults. People really don't give a 'monkeys' and have their own personal problems right now. I also feel much more confident with 'no hair' rather than bald patches- and yet at the time I hung on to every last hair nearly- funny how we adapt and change. Timd is certainly a great emotional healer!

Comment by Sandra Dubose-Gibson on August 30, 2011 at 12:33am

If you are live in North Carolina or in the surrounding areas, come on out and help me celebrate Alopecia Awareness Month at the NC Pubic Libraries. I am going on an eight city tour sharing my documentary film, "Project Liberation, My Alopecia Experience." The event is free and open to the public. There will be light refreshments, free door prizes, information and inspiration. Don't miss out. Space is limited so register to secure your seat today. Project Liberation Movement

Comment by Sandra Dubose-Gibson on August 30, 2011 at 12:29am

Comment by Terri on August 30, 2011 at 12:23am

this summer I created an awareness event in my city(Edmonton) with much success. With the local baseball team here, I had a great night bringing other alopecians out to join in and meeting eachother. Also to bring a little awareness of what alopecia is. My next goal is to do some school presentations with the help of my best friend who is a teacher.

Comment by Laura Adams on August 29, 2011 at 8:32pm

I use my difference and experience to try to help anyone going through a hard time, whether they are just losing their hair or have had it gone for years. I think I inspired one girl to write a book about her struggle and through that reach even more people struggling with hair loss and the ramifications thereof

Comment by Lili Añel (aka Eulalia) on August 7, 2011 at 1:12pm

Using my "difference" as an alopecian to help children with alopecia. Given they have their entire lives ahead of them with dealing with this, I advocate helping them in every way. To develop self-esteem and coping skills in a world seemingly hell-bent on emphasizing outward appearance as the ruler by which we are judged. I have organized an event whose proceeds will benefit Children's Alopecia Project who represent exactly what I support, the children. If you'd like to take a trip out for an excellent night of music and support CAP here's the info:

Tix and other info here: http://www.lilianel.org/mfcap.html

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