I just want to help and being so far away it is hard. If you need anything you better call me...I keep reading about this disease and it seems like it affects everyone so differently. I guess we'll just see where it goes...I'm here!
I am on this now. I want to be armed with information so that you don't have to go through it alone...I love you. No matter what happens with your hair you'll always be my beautiful, favorite cousin!
Hi Mandy! I know how you fee. I dreaded wearing a wig but at the same time I knew it would just be easier to be rid of my thin and patchy hair. I noticed that once I got used to a wig I didn't have to worry about wind blowing my bald spots into view and stuff like that. It's taken some time but I think I'm finally OK with this and it sounds like you're on the way to that train of thought too.
Hi Mandy, I wanted to welcome you to Alopecia World. I can honestly say that we are a great community here and I hope you enjoy the time you spend with us. Cheryl, co-founder
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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.