Hi Susan,
This sounds like a very stressful time for you. Have you considered joining a support group? I found this for you as a possible option:
National Alopecia Areata Foundation http://www.naaf.org/site/PageServer?pagename=support_resources_groups
Do you have family members who can share in getting your mom to treatment?
As a cancer survivor, I have experienced alopecia and a cranial defect. I understand how difficult it is when strangers stare (since I was bald and without a forehead).
Thank you for sharing your story.
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Hi Susan,
February 8, 2011 - 6:41pmThis sounds like a very stressful time for you. Have you considered joining a support group? I found this for you as a possible option:
National Alopecia Areata Foundation http://www.naaf.org/site/PageServer?pagename=support_resources_groups
Do you have family members who can share in getting your mom to treatment?
As a cancer survivor, I have experienced alopecia and a cranial defect. I understand how difficult it is when strangers stare (since I was bald and without a forehead).
Thank you for sharing your story.
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