Down's Syndrome

WHAT IS DOWN'S SYNDROME?

Down's Syndrome is caused by an extra chromosome and is there from birth. Having the extra chromosome is created by chance, although you may be more at risk if you are an older mother.  Those with Down's Syndrome will have some form of learning difficulty but this can vary hugely from person to person. Some will have good levels of independence and some may need more regular care. Down's Syndrome is often associated with common physical features such as being smaller than their peers, having smaller ears and low muscle tone. 

 

HOW IS DOWN'S SYNDROME DIAGNOSED? 

Down's Syndrome is diagnosed after a chromosome test to check for the extra chromosome.  This is done via a blood sample, which is sent off for analysis. Until the results have been returned, a diagnosis cannot be made.  Most people with Down's Syndrome will have been diagnosed in their first few months of life. 

 

WHAT HAPPENS AFTER DIAGNOSIS? 

There are a number of support services that can help.  Most children with Down's Syndrome will have regular check-ups with medical professionals to ensure physical health. Many CYP with Down's Syndrome attend mainstream nurseries, pre-schools and schools.  Education choices, as with all children, is wholly dependent on the individual child's needs. 

HOW CAN I FIND OUT MORE ABOUT DOWN'S SYNDROME? 

Please see here , here and here for further information. 

 

HOW CAN I HELP IN SCHOOL? 

Please see below for ideas on how to help.

Difficulty in communicating and learning in line with peers

Difficulties acquiring basic numeracy and literacy skills 

Short term or working memory difficulties 

Low muscle tone / Poor and fine gross motor skills

Emotional / behavioural difficulties