What is the Process for PGS?

For LGBTQ+ individuals and couples, Preimplantation Genetic Screening (PGS) plays a vital role in ensuring a successful surrogacy journey. At iBoyer, we are dedicated to providing inclusive and compassionate surrogacy services, including access to PGS for those looking to build their families.

What is PGS?

PGS is a type of genetic screening that checks embryos for chromosomal abnormalities before implantation. This process is particularly important for those undergoing IVF, as it increases the chances of a healthy pregnancy by identifying viable embryos free of genetic disorders.

The PGS Process Explained

  1. IVF and Embryo Creation: The first step involves creating embryos through IVF, using either the intended parents’ or donors’ eggs and sperm.
  2. Embryo Biopsy: A small number of cells are extracted from each embryo at a specific developmental stage.
  3. Genetic Testing: The biopsied cells are analyzed to detect chromosomal abnormalities, helping to identify the healthiest embryos.
  4. Embryo Selection: Only embryos with normal chromosomal counts are selected for implantation, enhancing the likelihood of a successful and healthy pregnancy.
  5. Embryo Transfer: The selected embryo(s) are transferred to the surrogate’s uterus to begin the pregnancy journey.

Why Choose PGS?

PGS helps improve pregnancy outcomes by minimizing the risk of genetic disorders, miscarriages, and failed IVF cycles. It offers LGBTQ+ families a reliable way to ensure their surrogacy process has the best chances of success, giving you greater peace of mind.

Interested in how PGS can help you on your path to parenthood? Visit iBoyer and contact our dedicated team today to learn more about our surrogacy services and schedule a consultation. Let us be your trusted partner on this beautiful journey to family-building!

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