www.alopeciaworld.com
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
Started by moonflower. Last reply by Angela Feb 12, 2014. 3 Replies 1 Like
Hi Ladies,It's certainly been awhile! How's everyone doing?-MContinue
Started by Ms. E Nov 2, 2013. 0 Replies 0 Likes
Wondering if anybody's listening?Continue
Started by Ms. E. Last reply by Ms. E Feb 28, 2013. 12 Replies 0 Likes
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
Started by Themba Shenge. Last reply by Ms. E Nov 10, 2012. 18 Replies 5 Likes
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
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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?
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 :)
Welcome CyberCindy34!
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.
Welcome Sweetnc!
Hello Dana and welcome!
Hi Dana! Welcome to Alopecia World & our group.
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
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