www.alopeciaworld.com
This can be a group where you discuss the good and the bad of Alopecia and how we can all help each other with our daily struggles. If someone is having a difficult time leaving the house without a wig or a hat then I would hope to help encourage you to become more comfortable with this condition. I also aspire in other situations we can all help each other over come fears that we have gained along the way. I sincerely want this group to grow and reach people who are new to this condition and hopefully make it easier for them to adjust. Anyone who wants to post a positive story or a discussion about an event or situation that happened to them because of Alopecia is greatly appreciated . Also if you would like to post a negative case then we can attempt to help you deal with your bad experience.
Members: 19
Latest Activity: Mar 22, 2017
Started by McKenzie Anne. Last reply by Dianna 845 Jan 28, 2016. 9 Replies 1 Like
Hello everyone I hope to see more people joining soon so we can begin helping each other and enjoying all stories that we share.Continue
Comment
So my names is McKenzie Hood I have had Alopecia Unervasalis for almost 16 years ive always went bald, never really liked hats or wigs but these last few years ive been getting more and more comfortable wearing wigs out and about. I have always taught myself that this condition isnt an insicurity and thats its nothing to hide or be ashamed of. Making sure that I am positive and looking at the bright side of Alopecia is a big part of how ive gotten through my life, Growing up with no hair is hard and you have a lot of bad days but you can get through them if you turly try and thats why I am here. I want to help others get hrough this the best and healthiest way possible. So please feel free to message me or post a disscussion to get things started. Thankyou.
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
You need to be a member of Hairless and Fearless to add comments!