Trying To Conceive? We are here to help on the genetics of all things preconception.

• IVF help -we can talk fertility testing and embryo testing

• Preconception carrier screening - we can arrange the 3 gene screen (free thanks to Medicare) or comprehensive testing of up to 1,300 genes and anywhere in between.

Once you are pregnant there are a few options you might like to consider when it comes to understanding the health of your baby.

• Carrier screening - know if you and your partner might be carriers of a genetic condition that could be passed on to your baby

• Non-invasive prenatal testing (NIPT) aka ‘Harmony test’

• Prenatal testing - amniocentesis or CVS

• Discussion about what to do if you get a high risk results form carrier screening, NIPT test or prenatal testing.

• Rhesus D non-invasive testing (RHD NIPT) -This blood test can predict if your baby is Rhesus negative or Rhesus positive

We are ready to partner with you in your reproductive journey here

Your child is growing and developing but you might have some concerns or your doctor has suggested some genetic testing. Here is some testing we can arrange:

• Chromosome microarray testing (CMA)

• Fragile X testing (FXS)

• Urine metabolic Screening (UMS)

• Whole exome sequencing (WES) and Whole genome sequencing (WGS)

DON’T DO A BLOOD TEST ON YOUR BABY -WE DO OUR TESTING ON SALIVA (and yes, it is just as good and accurate).

Really important period of development and growth. We are here to assess and revisit a diagnosis relating to genetic conditions such as:

• connective tissue disorders

• intellectual disability

• hearing and eye sight changes

• congenital heart defects

and much more. Book a 20minute call to find out if we can help.

This is your time to shine and live a long and healthy life and get to know your genes that relate to

• adult onset cancers

• cardiovascular disease

• neurological conditions

We can also arrange whole exome sequencing (WES) for complex adult conditions.

Let’s talk genetics for those curious people

Even if you’re a healthy adult without a strong personal or family history of disease, genetic testing can still provide valuable insights into how your genes might influence your health. Here are some things you might like to know:

• Genes that are known to significantly increase the risk of hereditary cancers, cardiovascular conditions, and other important medical concerns.

• Polygenic Risk Score (PRS) this is a whole new way of looking at our genes and is based on genome wide association studies (GWAS) and gives us powerful insight on the chances of someone developing a condition such as cancer, cardiovascular disease or Type 2 diabetes.

• Pharmacogenomics (PGx) which is the interaction between medication and our genes and why some people have adverse reactions. Stop the trail and error with your medication and consider PGx testing.