In addition, children and young people will need to have a blood test and an ultrasound scan or plain x-ray (or both). Taking shorts (for example) with you to this examination will make it easier for both parties. It can be helpful at diagnosis or just after to keep a folder for storing all information in one place. It’s easy to forget names, dates and times etc. The diagnosis is the first key step in determining the treatment plan. Once treatment starts the team’s aim will be to get the condition under control and ultimately into remission. Management includes medications, in conjunction with keeping your child active to increase stamina and strength. This will enable your child to get back to their daily activities and routine as soon as practicably possible.
4. Your child’s healthcare team explained Consultant paediatric rheumatologist or adult rheumatologist who sees children. The consultant will carry out a full examination and ask you lots of questions. He/she might also arrange for some blood samples to be taken, as well as x-rays and/or ultrasound scans. They will be responsible for diagnosing your child and they will also give you details of what the management plan will be (what they recommend to treat the JIA including physio, medication etc.) Here are some questions they might ask parent(s) of younger children: • What did you first notice was causing a problem for your child? • How long has this been going on? • Have you seen any different ways he/she has been doing everyday activities? • Has sleep been disturbed?
