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LIVING WITH ALOPECIA
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Debra De LaMotte of Roxbury is a stunning woman who has a stylish
way of dressing and wearing hats and scarves, and a classic face on
which she knows how to apply makeup skillfully. She has a job and a
boyfriend, and she wouldn't have any complaints about her life if
it weren't for one small thing.
De LaMotte has no hair. Not on her scalp, arms, eyelids or
legs. She's one of the estimated two million Americans of both
sexes and all ages who have the autoimmune disease called alopecia.
In her case it is alopecia universalis, meaning all the hair on the
entire body, not just the scalp, has ...
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