Sisters Living With Alopecia

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Sisters Living With Alopecia

If you or someone you love has Alopecia, don’t go through this experience alone. There may not be a medical cure for the condition but there is healing for your heart and mind and friends nearby who care.http://sisterslivinwithalopecia-com.webs.com/

Location: Little Rock, AR
Members: 71
Latest Activity: Aug 7, 2020

Discussion Forum

Hey strangers! :)

Started by moonflower. Last reply by Angela Feb 12, 2014. 3 Replies

Hi Ladies,It's certainly been awhile! How's everyone doing?-MContinue

Anybody here?

Started by Ms. E Nov 2, 2013. 0 Replies

Wondering if anybody's listening?Continue

Stupid Stuff People Say

Started by Ms. E. Last reply by Ms. E Feb 28, 2013. 12 Replies

I guess you could say I've got a wild hair (you know where)! :DI've been ranting and raving since I received the following e-mail earlier this evening:"Here's a question for you -- did you really cut…Continue

I just had to share

Started by Themba Shenge. Last reply by Ms. E Nov 10, 2012. 18 Replies

Hi beautiful ladies! I’ve FINALLY done it!Since August, gradually I started going out in public without a wig/hat. I found that it was easy to do this when going to a place where I knew no one i.e.…Continue

Comment Wall

Comment

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Comment by Missy on February 16, 2013 at 1:07pm

Hello ladies. I am new to this site. I have been wearing braids and weaves for years but at this point, I have to get a wig. There is just not much hair left to latch onto. Since this will be my first wig, I was wondering if anyone can give me their opinion on the best brands of wigs for black women?

Comment by Gerina on January 26, 2013 at 3:16pm

Hi girls! How is everyone? First winter without hair and I must say it has not been as cold as I expected it to be :)
I am disliking my wig more and more....a wig does not make it easier though the people around me think it does. Besides that it itches going from cold to warm temperature it has kept me less open about my condition which was kind of therapeutic for me. Anyone else experiencing this?

Hope I can kick in some more activity on this wall with my post :)

Comment by Angela on January 21, 2013 at 8:16pm

Welcome CyberCindy34!

Comment by CyberCindy34 on January 20, 2013 at 4:40pm

Hello Ladies, It been about two years since I was diagnosed with an autoimmune disorder and I am so glad that I have found this website as well. I have heard so many positive comments from others feedback on how they are dealing with alopecia. I wear wigs now because it makes my life easier and I've have changed to eating healthier foods. I look forward to getting information on Lupus or fibromyalgia because, I was told that I might have this in the future.

Comment by Angela on January 20, 2013 at 3:53pm

Welcome Sweetnc!

Comment by Angela on January 16, 2013 at 6:53pm

Hello Dana and welcome!

Comment by Nicole on January 16, 2013 at 9:40am

Hi Dana! Welcome to Alopecia World & our group.

Comment by MsDanaPatrice on January 16, 2013 at 3:26am
Hello all...I am new to the site...support groups actually. I have had alopecia since I was 9 years old and am interested in meeting others to hear their stories
Comment by Ms. E on December 25, 2012 at 11:30pm

Haven't been here in a while.
Thought I'd check and see how the day has been.
It looks like I'm not the only one who's been away.

Brenda, thank you for the compliment I'd not seen it before now. :)
Angela, a proud mommy I should say, on all accounts. :D

Comment by moonflower on December 1, 2012 at 11:02pm
Angela, your daughter seems so supportive and genuine. You are blessed!
 

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