The American Juvenile Arthritis Organization (AJAO) is a council of the Arthritis Foundation devoted to serving the needs of children, teens, and young adults with rheumatic diseases and their families.

Its members are parents, family members, doctors, educators, nurses, occupational and physical therapists, social workers, young adults, and anyone with a strong interest in arthritis in young people. Members of AJAO are automatically members of the Arthritis Foundation, a national voluntary health organization serving the 70 million people affected by arthritis.

AJAO's services help members better manage both the everyday and broader issues they confront.

AJAO groups in many Arthritis Foundation chapters encourage members to exchange ideas and offer support and friendship.

AJAO publishes educational materials ranging from free pamphlets to inexpensive self-help manuals. The bi-monthly newsletter "Kids Get Arthritis Too" keeps members up-to-date on related programs, services and current research. A wide variety of resources are also available.

American Juvenile Arthritis Organization's Vision Statement

As a council of the Arthritis Foundation, the American Juvenile Arthritis Organization leads the effort to improve the quality of life for those affected by childhood arthritis and related diseases.

This vision will be accomplished by:

• Increasing awareness of childhood arthritis and related diseases.
  
• Promoting access to care by a pediatric rheumatologist.
  
• Collaborating to develop and deliver education and support programs.
  
• Advocating for the needs of those affected by childhood arthritis and related diseases.
  
• Encouraging research and funding directed toward prevention, control and cure.

Learn more about AJAO.