Information

Alopecia Areata

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

Website: http://www.AlopeciaWorld.com
Members: 609
Latest Activity: Oct 9

Comment Wall

Comment

You need to be a member of Alopecia Areata to add comments!

Comment by TallNBald on October 9, 2016 at 8:54pm

Let's make bald great again! :)

https://www.gearbubble.com/baldgreatagain2

Comment by mcat111 on October 8, 2016 at 12:57am

Hello everyone.

Im newly diagnosed...it took while they thought for a long time i had AGA..i present that way i have christmas tree type part...turns out a Dr finally did a biopsy and have AA--so i am confused about my hair loss...it seems slow and steady and not looks like AA at all maybe very small patches like eraser head sized but many. Not clean circles either..I have a very tiny bit of one eyebrow mising--looks almost undetectable like i plucked a few wrong hairs (didn't)..i also notice a lot of white hairs on my brow..im 45 i assumed they were grey...

I am confused about how to proceed with treatment--this has been going on for over 5 years i would say and it's not very noticeable yet--but very thinned out on top..What i dont understand is people talk as if it happens very quickly...Also I have miniaturization similar to AGA--and these hairs short cycle.. My Dermatologist wants to do shots---but would a pill be better since its spread out??

Comment by Dr.mujib kazi on June 19, 2016 at 3:06pm
Hello friends
Comment by JeffreySF on November 3, 2015 at 10:50pm

Thanks for sharing Kevin!

Comment by kevin arnold on November 3, 2015 at 5:49pm

well its been a while since ive used this platform. For some odd reason, without medication and without care, ive experienced full regrowth for two years now. Dont know why or how and i dont care, with or without it im still me. So a shout out to others who have and know the emotional stress barring this condition, personally ive realized character is far more important than the outer shell and still today i truly believe the most beautiful people are those that are the happiest...so smile no matter what!!

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 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.
 

Members (609)

 
 
 

Badge

Loading…

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.

AlopeciaWorld.com: It's hair loss support at its best!

© 2016   Created by Alopecia World.   Powered by

Badges  |  Report an Issue  |  Terms of Service