Синдром Дауна
Синдром Дауна — это когда вы рождаетесь с дополнительной хромосомой.
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- What it's like to have Down's syndrome
- Having a baby with Down's syndrome
- Screening
- Important
- Advice for new parents Down's syndrome
- What life will be like
- How to help children and young people Down's syndrome
- Things you can do to help
- Medical support
- Support with education
- If your child needs more support
- Support for adults Down's syndrome
- Day-to-day life
- Choosing where you live
- Getting a job or volunteering
- Getting active
- Support for families and carers Down's syndrome
- Speak to parents and families
- Speak to a charity
- Other health conditions Down's syndrome
- More common health needs
- Other conditions
Down's syndrome is when you're born with an extra chromosome.
You usually get an extra chromosome by chance, because of a change in the sperm or egg before you're born.
This change does not happen because of anything anyone did before or during pregnancy.
What it's like to have Down's syndrome
People with Down's syndrome are likely to have some level of learning disability. This means they'll have a range of abilities.
Some people will be more independent and do things like get a job. Other people might need more regular care.
But, like everyone, people with Down's syndrome have:
- their own personalities
- things they like and dislike
- things that make them who they are
Having a baby with Down's syndrome
In almost all cases, Down's syndrome does not run in families.
Your chance of having a baby with Down's syndrome increases as you get older, but anyone can have a baby with Down's syndrome.
Speak to a GP if you want to find out more. They may be able to refer you to a genetic counsellor.
Screening
If you're pregnant, you'll be offered a screening test to find out your chance of having a baby with Down's syndrome.
You'll be offered the test between weeks 10 and 14 of pregnancy. It involves an ultrasound scan with a blood test. The blood test can be carried out at the same time as the 12-week scan.
If you have a higher chance, you can have further tests.
Important
It's your choice whether or not to have any screening tests.
Find out more about screening:
Advice for new parents Down's syndrome
Babies with Down's syndrome are like any newborn babies.
They'll be eating, sleeping, crying, and needing love and cuddles just like all babies.
Some babies with Down's syndrome might need extra help. This could be with things like feeding.
There's support available for whatever you or your baby needs.
What life will be like
No one can tell you what life will be like for your child. This is the same for children who do not have Down's syndrome.
Children with Down's syndrome are likely to have some level of learning disability – it's not possible to know how this will affect them.
Like any child they'll:
- have their own personality
- learn at their own pace
- have things that are important and unique to them
Try not to think too far ahead and enjoy time with your baby.
How to help children and young people Down's syndrome
Things you can do to help
Children and young people with Down's syndrome are likely to have some level of learning disability. This means they may need help with daily life.
What they need help with is different for each person. And this can change as they get older.
You can try these things to help with their development.
Do
- praise them when they learn something new
- speak clearly and calmly so they can learn from you
- play, sing songs and read books together to help with sounds and words
- try showing them how to do something instead of just giving instructions – this can be easier to follow
- try to set routines so they feel more settled – for example, for getting up and at mealtimes
- look out for changes in mood or behaviour – they may not be able to tell you if something's wrong or they're unwell
- take them for regular hearing, eyesight and health checks
Don’t
- do not talk down to people with Down's syndrome – treat them like anyone their age
- do not just talk to parents or carers, talk directly to people with Down's syndrome
Medical support
Children with Down's syndrome should have regular check-ups with a children's doctor (paediatrician) or a GP.
This is because there are conditions they may be more likely to have.
It could help for them to see:
- a speech and language therapist – for help with speaking
- a physiotherapist – for help walking if they have low muscle tone
- an optometrist or hearing specialist – for help with vision and hearing
- an occupational therapist – for help with their development
Speak to a GP, health visitor or your local council to find out how your child can get these services.
Support with education
Choosing a school or college
Lots of children with Down's syndrome go to mainstream schools.
There are also special schools and colleges for children and young people who might need more help.
Where your child goes depends on:
- the help your child needs
- what's available where you live
You can visit schools and colleges in your area and ask the staff how they can meet your child's needs.
Special educational needs support
Children with Down's syndrome will get special educational needs support at their school or college.
Special educational needs support might include things like:
- extra support from a teacher or assistant
- help taking part in lessons
- support with things like eating and getting around school
If your child needs more support
You can apply for an education, health and care plan (EHC plan, or EHCP).
This plan says what education and health needs your child has and what support they should get.
Having an EHC plan can either help:
- the school get extra money to support your child
- you apply for a place at a school that's better for your child
Support for adults Down's syndrome
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Day-to-day life
You may need help with day-to-day things like:
- cooking food
- cleaning
- shopping
- going to appointments
Your family, friends, carer, support worker or personal assistant can help you with these things if you need it.
If you need more support than you're currently getting:
- call the Down's Syndrome Association helpline on 0333 1212 300
Choosing where you live
You might be thinking about where you want to live.
There are lots of places you can choose.
For example, you could:
- live with your parents
- live in your own home
- live in a home with other people
Your family, carer or support worker can help you decide what you want to do.
You may be able to get some financial help with your living costs too.
Find out more:
Getting a job or volunteering
If you want to get a job, it might help to get in touch with the Down’s Syndrome Association.
They run WorkFit, which helps people with Down’s syndrome get paid jobs and voluntary work.
You or your carer can call 0333 1212 300 for more information.
You can also speak to a work coach at your local Jobcentre.
Find out more:
Getting active
Doing exercise can make you fitter, healthier and feel better. And it's a great way to meet people and make friends.
You can find out about activities near you from your local council.
The Down’s Syndrome Association also runs something called DSActive.
They have lots of things you can do like:
- football
- tennis
- athletics
- walking
Support for families and carers Down's syndrome
Supporting someone with Down's syndrome can be both rewarding and challenging.
If you need help, or just want someone to talk to, there's lots of support available.
Speak to parents and families
It can help to speak to other parents and families who know how you're feeling.
You can do this by:
- getting in touch with people on forums and social media
- going to a support group – ask your midwife or health visitor about local support groups
The Down's Syndrome Association also has a list of support groups:
Speak to a charity
You can get advice from charities such as:
Down's Syndrome Association
For people with Down's syndrome, their parents and carers.
- Phone: 0333 121 2300
Down Syndrome UK
For families and carers of children and young people with Down's syndrome.
- Phone: 0330 112 2121
Mencap
For people with learning disabilities and their families.
- Phone: 0808 808 1121
Contact
To support and bring together families with disabled children.
- Phone: 0808 808 3555
Other health conditions Down's syndrome
Important
If you have Down's syndrome, you should see a GP once a year for a check-up, so they can check your health.
This is because there are other health conditions you may be more likely to have.
Find out more about annual health checks.
More common health needs
Help with speech, language and communication
Children with Down's syndrome might need some help speaking.
A speech and language therapist can help. They can:
- check if your child needs any help with their speech
- suggest things you can do to help your child with their speech
Speak to a children's doctor (paediatrician), health visitor or GP who can refer your child to see a therapist.
Help with vision and hearing
People with Down's syndrome will need to have their sight and hearing regularly checked.
They may need to:
- wear glasses
- have a hearing aid
- see a specialist for help if they have something called glue ear
Speak to a children's doctor (paediatrician), health visitor or GP for more information.
Getting unwell with infections
People with Down's syndrome are more likely to have a weakened immune system (the body's defence system against infections). This means they can become seriously unwell when they catch any infection such as pneumonia or flu.
So it's also important to have all the vaccinations you should get.
It can also take longer for children and adults with Down's syndrome to get better when they are unwell. They're also more likely to need medical help and may need to go to hospital more often.
It can be difficult to tell when a baby or toddler is seriously ill, but the main thing is to trust your instincts and get medical help if you're worried.
You know better than anyone else what your child is usually like, so you'll know when something is wrong.
Other conditions
Heart conditions
Doctors will check your baby's heart soon after they're born.
This is because about half of all children with Down's syndrome are born with a heart condition (congenital heart disease).
If your baby has a heart condition it can sometimes get better on its own. But sometimes surgery is needed.
Speak to a children's doctor (paediatrician) to find out the next steps for your baby's care.
Autism
Some people with Down's syndrome can also have autism.
Common signs of autism include:
- finding it hard to understand what others are thinking or feeling
- getting very anxious about social situations
- finding it hard to make friends or preferring to be on your own
Find out more about signs of autism.
Alzheimer's and dementia
Adults with Down's syndrome should have regular check-ups from about the age of 30 to look for any possible signs of dementia.
This is because they can develop dementia at a younger age.
It can help to look out for signs such as:
- not being able to remember new things
- getting confused more easily
- finding it harder to understand what people are saying
Often these signs can be linked to conditions other than dementia.
But if you think someone you know is showing signs of dementia encourage them to speak to a GP.
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