Harmony of the Seas took two short 'preview cruises', three nights to Cherbourg and four nights to Rotterdam, after reaching port in Southampton on 17 May. Her first destination was Southampton, England, although her home port was Barcelona until 23 October 2016 when she crossed the Atlantic. After a construction time of 32 months, the ship first set sail on from the STX France docks in Saint-Nazaire, viewed by some 70,000 people. The vessel was floated out on 19 June 2015, began her first sea trials on 10 March 2016, and was delivered to Royal Caribbean on. Harmony of the Seas is named after the Harmony module on the International Space Station. The success of the first two Oasis-class ships led Royal Caribbean Cruises to order a third ship of the type in December 2012. History Harmony of the Seas as she appeared when being built at STX yards in France In length, however, Harmony of the Seas is the longest cruise ship in the world. With a gross tonnage of 226,963 GT, she is the third largest passenger ship in the world, larger than her older sisters Oasis of the Seas and Allure of the Seas, but surpassed by her newer sisters Symphony of the Seas and Wonder of the Seas. Harmony of the Seas is an Oasis-class cruise ship built by STX France at the Chantiers de l'Atlantique shipyard in Saint-Nazaire, France, for Royal Caribbean International. We’d be more than happy to discuss your concerns.Approximately 120,000 t (132,000 short tons) If you have any questions about your baby’s health and the tests you might need, please do not hesitate to reach out. An additional growth scan at 30-32 weeks can examine foetal growth. Therefore, we highly advise undergoing safe and non-invasive ultrasound scans at the 11-13- and 20-22-week milestones to check foetal anatomy and well-being. It doesn’t provide details on foetal growth, either. This includes heart and brain conditions and spina bifida. In addition, the Harmony Test doesn’t offer information on physical defects. 0.5% chance with single and 1% with twins. However, these procedures carry a risk of miscarriage. If this is your experience, you may wish to undergo invasive testing using chorionic villus sampling (CVS) or amniocentesis (amnio). If your 11-13-week scan shows a high nuchal translucency (3.5 mm or more) or significant defects (such as exomphalos, holoprosencephaly, heart abnormalities, or megacysis), the likelihood of rare chromosomal conditions may be elevated. While the Harmony Test provides accurate information about some chromosome conditions, it cannot detect others.įor example, this non-invasive prenatal test cannot provide information on some rare chromosomal abnormalities. The health of you and your baby are your priorities. If you would like to learn more about the above conditions and whether you are at a higher risk, please speak to your trusted doctor.

They may have heart, learning, or endocrine problems.

This condition occurs in females missing an X chromosome. Monosomy X, also known as Turner Syndrome.This can result in learning and behavioural difficulties and other health concerns in some cases. This condition occurs when a baby has differences in the number of X and Y chromosomes.

You can find out whether your baby is male or female – the Harmony Test can also determine the sex of twins. The Harmony Test can also be used to uncover additional information about your baby, including: Your pregnancy journey is unique, and we believe in patient-centred care that ensures you maintain control of your health.

Test results that indicate a less than 1 in 10,000 chance your baby has trisomy 21, trisomy 18, or trisomy 13 mean the likelihood is very low.

With 100% certainty, you can undergo Chorionic Villus Sampling (CVS), an Amniocentesis or Amnio tests.

Test results that indicate a high likelihood do not mean that your baby definitely has one of the conditions listed above.

An Non-Invasive Prenatal Test NIPT results show whether there is a high or low chance your baby has trisomy 21, trisomy 18, or trisomy 13.

Costo harmony test