Children and young people with arthritis

Early diagnosis and referral for young people with JIA

Children and young people with JIA require early diagnosis and referral for treatment to prevent life-long-term joint damage, pain, and disability. They and their families face the isolation and loneliness of having an often invisible and unpredictable condition that can affect both their physical and mental health without the right support and care. They also require developmentally appropriate materials in both health and school settings as well as support when transitioning to adult health services. 

Living with JIA in school can be very difficult for the children and young people living with the condition, but there are things schools can and should do to help. Schools have a statutory duty to support pupils with medical conditions. However, we know that far too many schools are failing to meet this duty.

Children and young people and their families or carers require support or signposting for associated mental health difficulties. They also require tailored support when transitioning to adult healthcare services to ensure they don’t fall through the cracks.