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Alopecia Areata

Join today to meet, support and share information and resources with others who are also living with patchy hair loss.

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Latest Activity: May 19

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Comment by BarbaraK on February 15, 2015 at 8:37pm

Hello,

It has been a while since I was diagnosed with Alopecia Areata. I notice every time I stress out I tend to have new bald patches. I like my wigs but they tend to be very hot.

Comment by Stacey B on July 24, 2014 at 3:06pm

My daughter was diagnosed with AA in 2010. 

Comment by Fascinatinrythm on July 11, 2014 at 12:22am

Hi all, My story began when I was 11-12 years of age,(1979-80), this was the first time I suffered from Alopecia. Back then it was called Alopecia Nervosa Type A. At the time I was a child actor. An Australian film I did called Mystery Island (1980), shows the hair loss in certain scenes. My hair did grow back after a few years. Now 35 years later I am experiencing alopecia (areata) hair loss again. It seems to be far more aggressive although I did not shave my head back then as I have done on this occasion. All signs show that it is the areata variety although the hair loss is also on my chin and around my mouth,(the goatee area).

Comment by Joyce Marie Hawes on December 14, 2013 at 7:05am

Hi everybody. Hope you have a wonderful Christmas and a great weekend. Merry Christmas my friends.

Comment by Deeann on October 19, 2013 at 4:34am

Just letting everyone here know about a book I'm working on.  It's really starting to take shape, and I'm looking for additional stories from men, women and children in all stages of hairloss.  

I've been featuring people who have made a difference with their experience by making choices to do something better, or to living up to their true potential. 

If you'd like to be part of this project, feel free to check out my website for "Head-On, Stories of Alopecia".  It can be seen at www.baldgirlsrock.com.  You can also see it on facebook under the "Head-On..." title.  I would love it if you could "like" and "share" it so it will continue to encourage more people to share their stories.

The alopecia community has always been so supportive of one another, and my hope is that word of this project will spread like wildfire. I look forward to hearing your story.

Comment by Amanda on June 26, 2013 at 10:18pm
I'm looking for ideas on shampoo and conditioner. Since my flare up this time my scalp is more sensitive than usual.
Comment by User306 on May 13, 2013 at 3:32am

Does anyone know where I could find some statistics? I want to know what % of people recover fully when they have Alopecia Areata but only have one spot.

 

I fully noticed it's presence 3 days ago! But 2-3 months ago, my boyfriend had pointed out that I was missing a little bit of hair but we both thought it was just my rosette...

 

I haven't seen any other spots...

Comment by JeffreySF on May 13, 2013 at 1:31am

Be well!!! Working nights is horrible on the body from my experience.

Hugz!

Comment by User306 on May 12, 2013 at 8:57pm

Just got diagnosed with this "condition"...i dont like calling it a disease. I'm not ill or disabled. I need to realize this and be grateful. I'm sad but im alive...right? right!

Going for a blood test and going back on a normal work schedule (no more night shift!)

Wish me luck!!!!! :-)

 

 

Comment by Joyce Marie Hawes on January 19, 2013 at 8:11pm

Hi everyone. I haven't been on here much. Well, the last wig I had was from my sister. She buys all the wigs for me every year on my birthday. She is a very great sister. I can't afford a real hair wig yet. Hows everyone doing? Did you have a great XMAS and are you having a good year? I'm still looking for a job. Hope everyone gets back to me. Have a great and warm weekend.

 

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