Sisters Living With Alopecia

Information

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

You need to be a member of Sisters Living With Alopecia to add comments!

Comment by Alopecian Beauty Mixer on May 31, 2017 at 5:59am
Hi guys I'm having a special Event called:
Alopecian Beauty Mixer (Charity Event)
(STRICTLY ENFORCED DRESSCODE NAVY BLUE & WHITE /CREAM ONLY) September is Alopecia Awareness Month thier ribbon color is navy blue so September 30, 2017, We'll be launching a fundraising campaign to support individuals who suffer from the diseases Alopecia Areata & Cancer. This is a family friendly event that will include networking, food, drinks, special guest, custom wig give aways/demos, complementary massages, makeovers and A lot more. Including a bartender for 21+ participants! We also will have live performances/Celebrity photographers are going to be in the building for personal and group shoots. Why not have a amazing time while supporting a positive cause? Lets come together as a community and show support, love, while giving back to one another! See you there...
Comment by StarShemaya on May 8, 2017 at 9:47am

Hello ladies!
I must be transparent. I do not have Alopecia. I was very nervous about joining this group because I feared that someone would be non-accepting of me just because I don't have Alopecia.

Let me tell you why I joined this group.

I really want to learn more about the life challenges and issues with living with Alopecia from someone who is actually living it.

You see, I've just retired from being a Certified Sisterlocks consultant for 15 years. I am in the hair business. I created Beautiful Hair Products about 10 years ago. Thank God that they've been received well in the world of natural hair care products industry.

I have always had a passion for hair. As a little girl, on into my adulthood, I've always wanted healthy long hair. Once I embraced 'locs' I have been able to experience length on my head.

My point. I want to connect and learn from those willing to share their stories with me. I want to learn how to relate on an emotional level with someone going through the challenges of living with Alopecia without offending them. I want to learn what is appropriate and what is not. How to be sensitive and understanding.

I have an online store in which I market my Beautiful Hair Products and Accessories and wigs. I have a listing of my store here on the AW Marketplace--Naturally Yours Boutique>> http://www.alopeciaworld.com/notes/Naturally_Yours_Boutique

There might be some of you who prefer wearing wigs and I would like to offer my collections to you. There might be some of you who still have hair and need a 'gentle' line of hair products without harsh detergents or chemicals; my BHP products is perfect for you.

I hope that none of you feel offended. For it is not my intention to do so.

I am glad I found this group and look forward to connecting with you.

Peace.
StarShemya

Comment by QueenPauPau on July 12, 2014 at 11:06pm

Hey Ladies, Sharing a little love from John Legend 

http://www.youtube.com/watch?v=Pi3bc9lS3rg

Comment by QueenPauPau on July 12, 2014 at 8:33pm

Deann, I love the website www.baldgirlsrock.com. It is very inspiring.

Comment by kymkym on May 13, 2014 at 12:11pm

Hello everyone, hope all of you are well and in good spirits.  I know it's been awhile and I am feeling better and have grown more accepting of my baldness these days.

Comment by Angela on February 12, 2014 at 5:07pm

Hello Ladies, Happy 2014!  Hope everyone is well.

Comment by Deeann on October 16, 2013 at 2:45am

Hi there. I'm so excited to release my website www.baldgirlsrock.com. I've had AU for the past 8 years, and AA for almost 30 before that. I've been working on a book for several years, and it's recently started to really take shape. I'm looking for 29 more stories from men, women and children from all over the world so we can all be fully represented. Please "like" my FB page Head-On, Stories of Alopecia to hear updates on how this project is coming together. I look forward to hearing from you, and to help tell your story.

Feel free to share the details of this message with others who have a story to tell. Thank you so much.

Comment by Angela on July 19, 2013 at 3:21pm

Hello Sisters! Just stopping by to give love, hope all is well with everyone. Be Blessed! Angela

Comment by Missy on February 16, 2013 at 1:12pm

Comment by Angela on February 16, 2013 at 1:10pm

Hello Missy and welcome. I buy all my wigs from www.hairsisters.com. I shop online and pick a wig I like and then I go to youtube and find video of ladies who have purchased the wig to see what it actually looks like. Every wig I have purchased has been great for me.

 

Members (70)

 
 
 

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.

© 2024   Created by Alopecia World.   Powered by

Badges  |  Report an Issue  |  Terms of Service