SAN FRANCISCO -- Jeanne Nollman was a later bloomer.
She waited and waited for puberty to hit, and when she was 17 and still nothing had happened, she got tested -- and found out she had a rare condition called Swyer syndrome and would need supplemental hormones.
What no one told her until eight years later, when she demanded more information about her condition, was that she had the male X-Y chromosome pattern.
"That was typical back then, in the '70s," said Nollman, now 51 and living in San Leandro, Calif., with her husband and two adopted teenage children. "I guess they thought I might go jump off a roof and commit suicide with this information. But I must be an odd duck because I was just relieved."
Now she's trying to help other children -- and their parents -- learn about and even embrace their "disorder of sex differentiation," or DSD. It's the medical term for hermaphrodite, a word no longer used by doctors and patients.