|
medical experts and State and national Down syndrome |
organizations, including physical, developmental, educational |
and psychosocial outcomes, life expectancy, clinical course, |
intellectual and functional development, and treatment |
options. The written information shall include contact |
information regarding first call programs and clearinghouses, |
national, State and local Down syndrome organizations, and |
other educational and support programs. The Department shall |
make this information available to persons who render prenatal |
care, postnatal care, or genetic counseling to parents who |
receive a prenatal or postnatal diagnosis of Down syndrome. The |
Department shall also make this information available to any |
person who has received a positive test result from a test for |
Down syndrome. The information provided under this Section |
shall be culturally and linguistically appropriate for a woman |
receiving a positive prenatal diagnosis of Down syndrome and |
for the family of a child receiving a postnatal diagnosis of |
Down syndrome.
|
Section 15. Distribution of information to parents. A |
health care provider who renders prenatal or postnatal care or |
genetic counselor who renders genetic counseling may, upon |
receipt of a positive test result from a test for Down |
syndrome, provide the expectant or new parent with the |
information provided by the Department under Section 10 of this |
Act.
|