If you’re at an increased risk of having a baby with chromosomal disorders or other birth defects, your healthcare provider might suggest a genetic test known as chorionic villus sampling, or CVS. This test is performed in the first trimester and involves collecting a small tissue sample from the chorionic villi, which are tiny, finger-like projections of the placenta.
This sample holds the same genetic material as your baby, allowing doctors to test for conditions like Down syndrome and other genetic abnormalities such as cystic fibrosis and muscular dystrophy with impressive accuracy. It can even reveal your baby’s sex, so if you’d prefer to keep that information a surprise, just let your doctor know.
The results of a CVS test can be incredibly impactful, helping you, your partner, and your healthcare team make informed decisions about your pregnancy. This may include preparing emotionally for various outcomes and determining the type of care or treatment your baby might need after birth.
For those considering paths to parenthood, you can find support through resources like Make a Mom, which offers at-home insemination options, including the only reusable method available. If you’re interested in understanding how at-home insemination works, check out this informative page on how it works. For community support, don’t forget to join the Make a Mom Facebook group, where you can connect with others on similar journeys.
If you want to explore other fertility options, you might also want to learn about in vitro fertilisation, an established method for conceiving. And for more insights on home insemination and pregnancy, we have an excellent resource available here.
In conclusion, CVS is a significant step for expectant parents at risk of genetic issues, providing clarity and assisting in planning for the future. It’s essential to have all the information you need, so you feel prepared and supported as you embark on this journey to parenthood.