Common Questions

You are being referred to us because we are one of only four centres in the UK that are designated to specialise in the type of craniofacial treatment your doctor thinks your child might have.

The four centres are among the best in the world and all work to the same standards. You are welcome to attend one of the other super-regional centres if you prefer. These are at:

• John Radcliffe Infirmary, Oxford
• Great Ormond Street Hospital, London
• Alder Hey Children’s Hospital, Liverpool

Unfortunately not, in most cases a scan is best done at our hospital, where the radiographer has a specialist understanding of the particular information we need.

Similarly, the blood tests we need are specific to the operation. It is best if they are done here by someone who knows exactly what we are looking for.

Not all children need operations. However, when we do operations, they typically last between four and six hours.

Our department is a world-leader in craniofacial operations. No operation is risk-free but with us, you are in the best possible hands. If you have any particular worries, please talk to Pete Noons, the nurse specialist, who will be able to answer many of your questions.

Yes. One parent can stay beside your child's bed during the stay in hospital. We will also try to get a room for the other parent in our hospital accommodation. Visiting is any time for parents and 10.00am to 8.00pm for other family members.

Children recover far more quickly than adults. Typically children are in hospital for five or six days after an operation. Most parents describe their children as being back to normal within a week of getting home.

That will depend on your child's condition. Some children need only one operation; others need a lot more. This is something members of our team will talk to you about when you meet them in clinic.

Yes. Your child's appearance is likely to be less distinctive after the operation. Although most parents are happy with the changes some parents feel saddened by this initially, as they are unfamiliar with the way their child looks. Do talk to the psychologist or nurse if you would like to.

The vast majority of children we treat don't need to go to Paediatric Intensive Care (PICU) after their operation. Our ward has very experienced nurses who are very used to caring for children who have had the type of surgery we perform.

That depends on the particular condition. Our speech and language therapy team is there to assess this and discuss it with you.

We will invite you back to our hospital at regular intervals for a few years to check your child and answer any questions that may have arisen, depending on your child's condition. In the meantime, you are welcome to call Pete Noons if you have any concerns.

When you are discharged from the hospital, your GP, community nurse and paediatrician will also be informed of your needs so you can be cared for nearer home.

It's good to talk to all your children honestly about what they can expect. We have found the following books helpful in preparing younger brothers and sisters for their sibling's operation. Both can be bought cheaply in good bookshops or online.

• Going to the Hospital (Usborne First Experiences) - Anna Civardi
• Topsy and Tim Go to Hospital - Jean Adamson

If you would like some help, do ask your nurse specialist.

At some point, your child will need to be able to explain his or her condition to other people. It's a good idea to take photographs of your child before the treatment and during the time in hospital. You can use these to tell your child what happened. They will also help your child tell the story for him or herself.

Do contact the psychology team if you would like further help with this.

We would recommend that you look at the following websites:

• Changing Faces
• Headlines, craniofacial support
• AboutFace, the craniofacial family society
• Craniosynostosis Support Group