Pre-Implantation Genetic Testing near Mobile, AL—Compassionate Guidance for Your Family-Building Journey 

Starting or growing your family is one of life’s most meaningful journeys. Along the way, having clear, trustworthy information can bring reassurance and peace of mind. Pre-implantation genetic testing (PGT) provides insight into embryos created during in vitro fertilization (IVF), helping you make informed, aligned decisions. 

At NewLIFE near Mobile, Alabama, our team combines advanced medical expertise with compassion, respect, and understanding of your values. We listen to your hopes, answer your questions, and guide you with care so that every step aligns with your vision for your family. 

How Pre-Implantation Genetic Testing Works 

PGT is performed during an IVF cycle before embryos are transferred to the uterus. The testing allows our fertility specialists to screen for potential genetic or chromosomal conditions, giving you information about which embryos may have the strongest chance of successful implantation. 

This process is optional and considered only when it aligns with your health, family planning goals, and personal values. Many families choose genetic carrier screening beforehand to gain even more understanding about inherited conditions, which helps guide ethical and informed decision-making. 

Types of PGT 

PGT-A (Aneuploidy): 

Checks chromosome numbers to identify differences that could affect implantation or miscarriage. 

PGT-M (Monogenic Disorders): 

Screens for single-gene conditions, such as sickle cell disease or Huntington’s disease, when one or both partners are carriers. 

PGT-P (Polygenic):  

Assesses risk for more complex conditions influenced by multiple genes, such as diabetes, certain cancers, or heart disease. 

Each test provides information to guide your decisions—always with the understanding that PGT is a tool for awareness, not a directive. It supports your choices while honoring yyour family’s unique path. 

Who May Benefit from PGT 

PGT is not necessary for every IVF journey, but it can provide valuable guidance if: 

• One or both partners are carriers of genetic conditions 

• Previous IVF cycles did not result in pregnancy 

• Multiple miscarriages have occurred 

• Fertility challenges remain unexplained 

• The birthing parent is age 38 or older 

• LGBTQ+ individuals or couples are building families through IVF 

Your reproductive specialist will review your situation gently, thoroughly, and without pressure. Our goal is to provide clarity, answer your questions, and help you make decisions that align with both medical and scientific guidance and your personal goals and values. 

How Embryo Testing Is Done 

A small sample of cells is carefully removed from the outer layer of the embryo (where the placenta will form) for genetic testing. The embryo will be monitored under controlled laboratory conditions throughout the testing process. 

Our embryologists are highly trained, following strict protocols to maintain accuracy and security. The NewLIFE IVF lab uses state-of-the-art monitoring systems, climate controls, and backup measures to ensure the safety of your embryos while testing is completed. 

When results are ready, your fertility team explains them in clear, compassionate terms, helping you understand the information without feeling overwhelmed.