Comment by Ktownnana on September 21, 2011 at 9:37pm

Because of this web site, yesterday was a milestone marker for me. I went to my eye dr. and
he commented how pretty my hair was and I blurted out--it's a wig--I have Alopecia. He said
he would never have known and he said I'm looking thru a microscope. Before I discovered this
web site, I would never have admitted--especially to my eye dr.--that I was wearing a wig. Thanks to all the members who have helped me realize that I am not in this alone.

Comment by Bald and Fabulous AKA Terri on September 21, 2011 at 10:48pm

Without the support of this site I would never be so open about my alopecia today or embarking in all that I'm doing to bring awareness to this disease. I wish there was such a site when I was a kid but so grateful that its here today all those newly diagnosed with alopecia
Thank you alopecia world

Comment by Mary on September 21, 2011 at 11:00pm

We all owe SO much to you and Cheryl! WE can never thank you enough for creating Alopecia World.

Comment by Susan P aka DGADBS on September 22, 2011 at 6:54am

I would like to thank you and Cheryl, this site gave me the courage to accept my Alopecia. I joined the day I decided to shave what remained of my hair and Cheryl was there for me in an instant! I went out the door for the first time as a bald woman and it's all because I saw so many beautiful bald women on this site and realized I could do it too!

Comment by Alliegator on September 22, 2011 at 3:54pm

I am impressed also. Thank you! HUGS! I wouldn't be where I am at today if it wasn't for everyone's support. I really appreciate this website and all of the wonderful members.

Comment by lovelyjan on September 22, 2011 at 9:27pm

Thank you Cheryl!!! This site has open up a whole new way of living life with AU. I am not afraid anymore for the world to see me for who I am. Much Love to my new AW Families.

Comment by Pamela Rosse on September 23, 2011 at 6:48pm

R.J. & Cheryl
Mahalo Nui Loa is Hawiian for thank you from the heart & that is exactly where my thank you comes from my heart for not only the creation of Alopecia World but also the two of you. For you are the heart & soul of Alopecia World, you two are extroadanary human beings who lead by example, youbare the type of human being we should all strive to be like. I am so very proud & grateful to a part of this community. Mahalo Nui.

Comment by ROSE WOSE on September 28, 2011 at 11:00pm

WHAT I TRULY FEEL AFTER BEING A MEMEBER HERE FOR ONLY A FEW MONTHS IS LOVE , ACCEPTANCE ,RESPECT AND SUPPORT. I HAVE FOUND A WHOLE BUNCH OF FRIENDS THAT MAKE ME PROUD TO BELONG. LIFE IS GOOD THANKS TO MANY OF YOU ....I CAN NOW FOCUS ON WHAT IS REALLY IMPORTANT IN LIFE THANKS TO ALL OF YOU....EVEN IN SHORT VISITS TO THE WEBSITE I CAN FEEL THE LOVE...HUGS ROSE

Comment by Shelli Marling on October 25, 2011 at 8:12am

LeNae has had Alopecia since she was 2 and is now 6. I read what I can on this and try to let the schools know more about it. She is very healthy bouncing off the walls kinda girl.. She is my little entertainer and loves life to the fullest. I appreciate this site and the info. and stories of others. Thank U very much for all that U are doing for others. Blessed Be. ~smiles~

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