I am a wig designer with my own business call C&S Sensational Wigs-N-Extension Boutique please take a look at our facebook page which is link to our website http://www.cssensationalwigsnextension.weebly.com I have lived with alopecia areata for 18 years and I’ve experienced the rollercoaster emotions associated with it. I’ve lost my hair four times and I’ve regrown it three times. Both the course of the condition and the associated emotions can be unpredictable and the lack of control of your own body is frightening and intimidating. I have found that others accept me with my alopecia areata but only after I have accepted myself first. That wasn’t easy as I had to learn to accept the new me. It’s easy to glue on your eyelashes, draw on your eyebrows and to tape on your wig, but it’s hard to mend your heart and your spirit. This can only be accomplished when you accept who you are and how you are. Only then can others help you. I’ve been fortunate to have a very loving family and a great support group of friends and they’ve helped me through the alopecia areata good times and the bad, the denial and the acceptance, the loss and the growth and the struggles and the successes.
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.
Comment Wall
You need to be a member of Alopecia World to add comments!
Join Alopecia World