Alopecia World member Willow recently wrote us and gave our beloved community a wonderful compliment. She wrote, "I think your web(site) is a miracle to some people, a helping hand to some, but it's an extended family to us all."

We are grateful beyond words that Alopecia World has come to mean so much to so many people. Not just the more than 1,200 amazing individuals who are now registered members, but also the thousands of unregistered visitors who hang out in Alopecia World each month!

Any time you desire to do so, send us positive feedback and even suggestions for improving Alopecia World. In fact, please take a moment to reply to this blog and share what Alopecia World means to you.

Looking forward to hearing from each of you,

richard jones (rj) & Cheryl Carvery
Founders, Alopecia World

Views: 9

Comment by nathalie on July 6, 2008 at 7:43am
since I know this wonderful website , for the first time of my life I feel normal even if I'm different because every person on this website is kind and has a particular sensibility and meet people like me reassured myself and help me to see that alopecia is not a shame and it's also beautiful
thank you each other for being so kind and lovely
this website brings me sincerity, friendship and faith
thanks a lot and excuse my english!
take care of you and go on you're not alone anymore
Comment by paula on July 6, 2008 at 8:59am
i wish i had had a support such as this when i got alopecia 25 years ago. i was scared, embaraassed, and there really was no where to turn. i was only 28, single, and didn't know how to tell my dates about my condition so i just preteneded it wasn't happening.
i went to a therapist and he told me i needed to explore my relationship with my mother to better understand why i was losing my hair! ugh! i am so thankful that we have so much information, support, and technology these days so that we can all talk amongst ourselves, attend seminars and support groups, and wear beautiful naturual looking hair pieces if we choose to! i love you all out there and i hope we all can be there for each other in times of need! paula
Comment by as on July 6, 2008 at 1:39pm
I have got baldness only several months.Have had bonanza, that the at once on beginning his bald walking,am found this inspired place.Much me helped reading commentaries members.Mostly but view of beautiful bald women,their bravery and inner eye - appeal,are for me big instance,how manage its baldness and no feel other.I would like you that much tell,unfortunately I I don't know English,so for me please not to be angry.Thank you,thank you to all!!! as
Comment by Nicole on July 6, 2008 at 8:20pm
I've only been apart of Alopecia World for a short time but to me it's a place where I can get some information on AA (and all Alopecia types) from those who have it (and have had it many years). It's a place where I can get support from other mom's who have Kids with Alopecia and are feeling the same as I am and also from the rest of the AW members.
Comment by Carol on July 7, 2008 at 7:47am
If it wasn't for Alopecia World, I don't know if I ever would have been able to find the inspiration to start my local support group. Thank You!
Comment by Mandy on July 7, 2008 at 10:34am
Alopecia World means sooo much to me. I am so grateful to have found this website right away when I was diagnosed. Because of this website I was able to learn so much from real people...rather than just reading facts (and some fiction) on other websites. Because of this I was able to accept my condition very very quickly and for that I am so grateful. I tell everyone I meet about this website. This website has also allowed me the opportunity to create a group for those in Chicagoland which in turn has allowed me to meet others with Alopecia in my area. I can't say enough. Thank you!
Comment by chelsi on July 7, 2008 at 11:27am
I would like come in more often , but i speak only in french and it's too difficult to read in english. Thanks
Comment by Emma on July 7, 2008 at 5:20pm
I am so grateful i was told about this website, everyone is so supportive of everyone, it has helped me - in the last 3 months this photo was a "never gonna happen" and look at me in these short months i have been a member of this community i have become so much more content within my self, i am wearing my wigs less and less - i don't think i will ever stop wearing them because i like the way i can change my look in an instant. Thanks
Comment by willow on July 7, 2008 at 6:09pm
Thank you Richard and Cheryl for honouring me, by quoting me, and I'm so glad many agree how much a god send this site is for so many. I've had alopecia for almost 4o yrs, and some days, yes it bothers me. It's wonderful to know, we are not alone. I said to my husband yesturday, How I wish, Alopecia World was around years ago, how much it would have impacted my life. I am so grateful, you'se made this site, for all of us. Brightest of Blessings to all.
Comment by Roger on July 7, 2008 at 8:05pm
RJ and Cheryl.

Im really glad to have met you in real life. I hope to get more time with you next summer in Houston. I have new friends through this community. And in Louisville I met some of them for the first time and for that im very grateful.

Tack (thanks)! As they say here in Sweden.

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