Down’s Syndrome Norfolk

Due to Covid-19 all DSN activities are suspended until further notice. We can still be contacted for advice and support.

Experience shows that other parents are often the best source of information and support.  

We can all benefit by pooling knowledge and working together.  

Who are we and what do we do? 

Down’s Syndrome Norfolk serves its members throughout the county by:

  • Providing information, advice and support. –   ‘We Love Our Lives !’  is a series of 12 short films featuring some of our members celebrating their lives, click on the menu link above to view.

  • Working with and alongside the statutory agencies (Health, Education and Social Services) and other voluntary organisations.

  • Supporting new parents.

  • Organising activities such as The Young Down’s Group

  • Organising social and fundraising events.

  • Promoting the education of children with Down’s Syndrome in mainstream schools to fulfill their potential.

  • Encouraging the provision of more training and support for staff in schools.

DSN supports the Down’s Syndrome Association (DSA) in their ambition to enable people with Down’s Syndrome to lead a life of their OWN CHOOSING

What is Down’s syndrome ?

There are approximately two babies born with Down’s Syndrome in the UK every day.

There are around 60,000 people with Down’s Syndrome living in the UK today.

Down’s Syndrome is the most common form of ‘learning difficulty’.

Down’s Syndrome occurs at around the time of conception giving rise to an extra copy of chromosome 21 in each of the baby’s cells. It is a ‘genetic’ condition. We do no know why it happens. It can happen to anyone.

People with the syndrome will experience varying degrees of learning difficulty but most will, with appropriate support, achieve and live healthy, rich and varied lives.

Down’s Syndrome was first described by Dr John Langdon Down in 1866 – hence the name, but its genetic nature was not discovered until 1959.

Down’s Syndrome is not an illness; people do no ‘suffer’ from it.

People with Down’s Syndrome are all individuals. Each has his or her own personality and family traits. Down’s Syndrome is only a small part of who they are.

‘We Love Our Lives !’ is a series of 12 short films featuring some of our members celebrating their lives, click on the menu link above to view.

Useful Literature About Down’s Syndrome:

Down’s Syndrome – The Facts…………………………… Mark Selikowitz

Down’s Syndrome – An Introduction For Parents…………………(new edition 2004/5)

New and Expectant Parents

You are over the moon. Then you are told that your baby has Down’s Syndrome. Your world is turned upside down.

You have so many questions and anxieties. Who can you turn to for sensitive, practical and informed advice?

Part of the work of Down’s Syndrome Norfolk (DSN) is to provide support and information to new and expectant parents of a baby with Down’s Syndrome.

We have trained parent members who can visit you at home, in hospital or have a friendly chat on the telephone.

We run The Young Down’s Group – a group for young children with Down’s Syndrome, especially babies and those of pre-school age, and their families.

If you are a new or expectant parent of a baby with Down’s Syndrome and would like to have a chat with one of our trained parent members email us at:

or phone Chrystal, on:


Other useful addresses and websites:

Down’s Syndrome Association (DSA)
Langdon Down Centre
2a Langdon Park
Middlesex, TW11 9PS

0845 230 0372

Down’s Heart Group (DHG)
PO Box 4260

0300 102 1644

DSN Young Downs Group

Due to Covid-19 all DSN activities are suspended until further notice. We can still be contacted for advice and support.

One of our most successful and popular activities is the running of this support group for families, carers and friends of babies and children who have Down’s Syndrome; and who are aged from birth to eleven years.

The Young Down’s Group (YDG) gives children a chance to play together and have some fun, whilst parents socialise and exchange views and ideas over a cuppa.

The Young Down’s Group is held on the first Saturday of every month (except: January, August and September) 10:00 – 12:00 at:

Harford communuty Centre
10 the lastings
Hall Road
NR4  6ET
Young Down’s Group Venue

There’s plenty of room for grown-ups to relax with refreshments and (as often as possible) meet with invited speakers, plus older siblings are able to use the school hall and playing fields.

Kate’s Crafty Corner: As always, Kate is on hand at every YDG session to guide youngsters with one of her fabulous craft activities.

There’s ample car parking on-site and the Centre is seconds from the Ring Road and easily accessible from the A47.

Everyone at Down’s Syndrome Norfolk and the Young Down’s Group extend a warm welcome to our new families, and look forward to seeing you again soon.

The YDG still remains a great opportunity for all ages to meet up with friends, siblings, parents/carers and grandparents.  Come and meet some of our younger and more recent members.

For further information about The Young Down’s Group contact:

Chrystal, on:  07968655703

or email:

DSN Contacts

Down’s Syndrome Norfolk (DSN) Registered Charity number 1098031


6 Manor road
IP22 5QU

For further information about DSN contact:

For further information about YDG (or if you are a new parent) contact:

Chrystal, on:   07968655703

All emails are treated with confidentiality, details will not be divulged to any third parties.