What is Down’s syndrome? Typically, people will have 46 Chromosomes, however an individual with Down’s syndrome will have three copies of the 21st chromosome making 47, this is what we call Trisomy 21.

A baby being born with Down’s syndrome isn’t as a result of anything you did or didn’t do and it isn’t hereditary. It simply occurs during conception. Did you know only 20% of eggs carrying the extra 21st chromosome survive the first cell division? And of that 20% approximately only 20% of those survive to fertilisation? And of that 20% only 20% then survive the first cell division after fertilisation! Which goes some way to showing how amazing all our children are, they are strong and defy the odds.
We do not know what causes the extra chromosome. It occurs in all races, social classes and in all countries throughout the world. It can happen to anyone.
Whilst there are characteristics that people with Down’s syndrome share, such as those beautiful almond eyes, a palmer’s crease and button nose, they are so much more like you and your family than you may realise now. A baby with Down’s syndrome needs love and security just like any other child.

After receiving your diagnosis, you may be concerned for what the future holds for both you and your little one. Whilst they may need additional support first and foremost, they are your baby with all the same wants and needs.
Your child will bring you laughter, joy and tears like any other child.
Your midwife or local hospital should provide you with information packs on resources available to you. If you do not receive this or would like additional information, please do not hesitate to contact us
(newparent@swindondownsgroup.org.uk)
As a new parent we will provide you with a Congratulation box which will contain information and a gift
for your new-born. We also have a dedicated pack for expectant parents.
New Parent Contact - Swindon
Hello, I’m Jodie and this is my son Kylo who was diagnosed with Down’s syndrome at birth. We made contact with the Swindon Down’s Syndrome Group a few days after he was born and have had so much support and made some great friendships. Jump ahead a few years and I am now a new parent contact, supporting parents going through the same journey.
New Parent Contact - Wiltshire
Hello, I’m Cherylin and this is my amazing son Milo who was diagnosed with Down’s syndrome at birth. Milo is now 15. Yes, there have been challenges there have also been lots of fun and adventures. I am now one of the new parent contacts and happy to talk to any families with a new baby who may have questions or just want to talk. I am are here to support you and offer help where I can.