Genetic Counselling
We offer comprehensive genetic counselling to support you and your family in understanding and managing any genetic health risks.
Our experienced genetic counsellors provide personalised guidance on a wide range of testing options, including Non‑Invasive Prenatal Testing (NIPT) and reproductive carrier screening. Our aim is to give you clear, thoughtful information so you can make decisions about your reproductive health with confidence. We take the time to explain each option, what the results might mean for you and your family, and the choices available to you. Your genetic counsellor will work closely with you, at your pace, to ensure you feel informed, supported and never rushed.
There are several reasons why you might seek genetic counselling
f you have a family history of genetic conditions, such as cystic fibrosis or muscular dystrophy, genetic counselling can help you understand the chance of these conditions being passed on to your children.
Your genetic counsellor will talk through your family history in detail, explain your individual and reproductive risks in clear terms, and discuss the testing and support options available, so you can make choices that feel right for you and your family.
Couples planning a pregnancy can also benefit from genetic counselling to better understand their chances of passing on any inherited conditions.
Talking with a genetic counsellor before you conceive can offer reassurance, highlight any risks early, and support you in making thoughtful decisions about family planning, based on clear information tailored to you and your partner.
If you receive an unexpected or abnormal result from a prenatal screening test, genetic counselling can offer clear information and gentle guidance about what this might mean.
Our counsellors will take the time to explain your results, discuss their possible implications for you and your baby, and talk through any further testing or management options. We’re here to answer your questions, support you emotionally, and help you decide on the next steps that feel right for you and your family.
If you have experienced pregnancy complications that may be related to a genetic condition such as miscarriage or stillbirth, genetic counselling can help explore possible underlying causes and what they might mean for you.
Your genetic counsellor will review your history in detail, discuss appropriate testing options, and help you understand any results and how they may influence future pregnancies. Throughout this process, we aim to provide both clear information and compassionate support, so you feel as prepared and supported as possible moving forward.
Our clinic offers a wide range of genetic testing options to address different questions and concerns you may have.
Non‑invasive prenatal testing (NIPT) is a safe, highly effective blood test that screens for certain chromosomal conditions in a developing baby.
It works by analysing tiny fragments of your baby’s DNA (cell‑free fetal DNA) that circulate in your bloodstream during pregnancy. From this sample, NIPT can estimate the chance of conditions such as Down syndrome (trisomy 21), trisomy 18 and trisomy 13.
Because it only involves a simple blood draw from your arm and poses no risk to the pregnancy, many parents find NIPT a reassuring and accessible first step in understanding their baby’s chromosomal health.
Reproductive carrier screening looks to see whether you carry certain genetic changes that could be passed on to a child.
It’s especially recommended for couples planning a pregnancy or those using assisted reproductive technologies, but can be helpful for anyone wanting to better understand their reproductive risks. Carrier screening can look for conditions such as cystic fibrosis, spinal muscular atrophy and fragile X syndrome, providing valuable information to support informed, thoughtful family‑planning decisions.
Our genetic counsellors take the time to understand your unique situation, listen to your concerns, answer your questions and offer clear, gentle guidance. We work closely with your other healthcare providers to ensure well‑coordinated care and to support the best possible outcomes for you and your family.
Our state‑of‑the‑art clinic is equipped with the latest technology to provide accurate, reliable testing. Your privacy is a priority- every consultation is conducted in a confidential, respectful and supportive environment, where you can feel safe to talk openly about your options and preferences.
Non‑invasive prenatal testing (NIPT) is currently the most commonly requested early pregnancy screening test. It looks at small fragments of your baby’s DNA in your blood to assess the chance of trisomy 21 (Down syndrome) and other common chromosomal conditions.
Another important option for screening is the Combined First Trimester Screen (CFTS), previously known as the Nuchal Translucency scan. Even if you choose to have NIPT, CFTS is still recommended, as it provides additional information about your baby’s development and the pregnancy that NIPT alone cannot offer.
Bundle Inclusions
- Genetic Counselling by our Genetic Counsellor
- Viability Scan approx. 10 weeks’
- Genetic Carrier Screening
- First Trimester Nuchal Bloods
- Pre-Eclampsia (blood pressure) Screening
- NIPT^
- Early Anatomy Scan
- Scans completed, and reported on by Intuition’s Maternal Fetal Medicine Specialist
Get in touch
If you wish to make a booking with one of our specialists or allied health team, please get in touch with our friendly support staff.
We understand the need for women-led care and have an easy referral system to other health care professionals who provide a range of services specialised to your individual needs.