
Spina bifida: Olivia's story —
Olivia Jackman was born in September with spina bifida, a type of neural tube birth defect. Spina bifida is a birth defect in which the vertebrae do not form completely around the spinal cord.

Spina bifida: Olivia's story —
Olivia had surgery two days after birth. Spina bifida is the most common neural tube defect, affecting 1,500 to 2,000 of the more than 4 million babies born in the United States each year, according to the National Institutes of Health.

Spina bifida: Olivia's story —
There is no cure for spina bifida, and treatment depends on the type and severity of the disorder, the NIH says.

Spina bifida: Olivia's story —
Olivia is undergoing physical and occupational therapy and doing well, says her mother, Andrea Jackman.

Spina bifida: Olivia's story —
Doctors are hopeful Olivia will walk with the assistance of leg braces when she gets older.

Spina bifida: Olivia's story —
Olivia's mother says she is willing to work with Washington state epidemiologists investigating the cause of a cluster of birth defects such as her daughter's if it would prevent another family from having a baby with such defects.


