Preimplantation Genetic Screening (PGS) is an essential step for many intended parents considering surrogacy. At SurroCare, we understand how critical it is to ensure a healthy pregnancy and child, which is why we offer comprehensive support for those opting for PGS as part of their journey to parenthood.
What is PGS?
PGS is a genetic test performed on embryos during an IVF cycle before they are implanted into the surrogate’s uterus. The purpose of PGS is to identify embryos with the correct number of chromosomes, reducing the risk of genetic disorders and increasing the chances of a successful pregnancy.
Step-by-Step PGS Process
- IVF and Embryo Creation: The intended parents (or egg/sperm donors) undergo IVF to create embryos in a laboratory setting.
- Biopsy of Embryos: Once the embryos reach a certain stage of development, a small biopsy is taken from each embryo.
- Genetic Analysis: The cells extracted from the embryos are tested to check for chromosomal abnormalities, such as Down syndrome or other conditions.
- Selection of Healthy Embryos: Only embryos with the correct number of chromosomes are selected for implantation, increasing the likelihood of a healthy pregnancy.
- Embryo Transfer: The selected embryo(s) are then transferred into the surrogate’s uterus to begin the pregnancy.
Why PGS?
PGS can help reduce the chances of miscarriage, increase pregnancy success rates, and offer peace of mind to intended parents. It’s especially important for couples or individuals with a history of genetic disorders or those using IVF to overcome fertility challenges.
Ready to learn more about how PGS can help you on your surrogacy journey? Visit SurroCare to explore our comprehensive surrogacy services and schedule a consultation with our experts. Let us support you every step of the way to ensure a healthy and happy future for your family!