What if you or someone you know would benefit from from catching a glimpse into the lives of people living every day with hair loss in our hair obsessed world? Perhaps someone with alopecia, or undergoing chemo or radiation therapies or coping with trichotillomania, hormone imbalance,lupus or genetic balding? Is there anything you can do to help yourself or assist your friend or loved one?
In this episode 2, Deeann Callis Graham has Alopecia Universalis, complete loss of all body hair. She could have chosen to hide away from view under hot itchy wigs and head coverings for the rest of her life. It's easy to do when you don't know anyone else with visible hair loss and you feel isolated and alone.
Deeann chose to reach out. She found her way online support groups and a National Alopecia Areata Foundation annual conference and was in awe looking at all the openly and happy bald people there. She made life long friends at the conference, and goes back year after year.
Deeann had a realization that she could help others who feel as isolated and alone as she did by collecting stories and professionally shot photographs of bald women, men and children and publish their stories in book form.
Listen to her share her amazement when she asked for stories and was deluged with over 500 submissions. Deeann tells us about the process of putting her book together. She shares what it has come to mean to her and how it has touched others and loosened the grip of isolation. And she hints at future plans.
You can learn more about Deeann and her book on her facebook page, Head On, Stories of Alopecia and her website, www.headonpublishing.com
This episode hosted by Pam Fitros, author of Boldly Bald Women, www.BoldlyBaldWomen.com