1. What are the advantages of the DNA-based blood test over other CF screening tests for my situation?

2. When is the best time for me (or us) to have a CF screening test?

3. Should my child be tested for CF?

4. Does the state require or offer newborn screening for CF? Do I need to request it?

5. How do our race and ethnic background affect our risk for CF? Do certain CF panels contain more mutations specific to my race or ethnicity? Do you have enough information on my ethnic background and family history to guide the lab?

6. What are the advantages and disadvantages to both parents being tested? Do you recommend being tested at the same time or at different times?

7. In terms of both advising me on the value of CF screening and interpreting the findings on the lab report, are you comfortable discussing the genetic aspects or would you recommend a meeting with a genetic counselor or medical geneticist?

8. Are there others in my family who may be carriers and would benefit from knowing the findings of our CF tests?