What is genetic counseling?
Genetic counseling is a dedicated conversation with Dr. Chandak to help you understand genetic or chromosomal risk relevant to your pregnancy โ in plain language, without jargon, and without pressure toward any particular decision.
When is genetic counseling recommended?
- A screening test (NT scan, combined screening, or NIPT) has shown a higher-than-average risk
- An anomaly scan has picked up a "soft marker" or structural finding that needs explaining
- There is a family history of a genetic condition or chromosomal disorder
- You have previously had a pregnancy affected by a genetic condition
- You are simply looking to understand your options before deciding on any screening or testing
What happens during the session
Dr. Chandak reviews your personal and family history, along with any scan or test results you bring. She explains what any risk figures actually mean in practical terms, walks you through the testing options available โ including NIPT, amniocentesis, or CVS โ and discusses what a result would mean either way.
Our approach: non-directive, always
What happens after
If you decide to proceed with further testing, Dr. Chandak will guide you through the next steps. If results come back showing a genetic condition, a further counseling session helps you understand what it means for your baby, for delivery planning, and for future pregnancies.
Frequently asked questions
No. Counseling is about giving you information and options โ whether and what to test for afterward is entirely your decision.
No, any parent can request it. Many find it helpful even with a low-risk pregnancy, simply to understand their options.
Dr. Chandak will explain exactly what the finding means for your specific situation, discuss all available options, and support you through whatever decision you make, connecting you to further specialist care as needed.