Champion of Yes has come to mean different things to different people. To many, it means refusing to let arthritis win – to stand up, push back and say, “Enough is enough. I won’t let arthritis stop me or anyone else from living life to its fullest!”
Kids get arthritis, too! And we at the Arthritis Foundation are dedicated to being their champions. According to the Centers for Disease Control and Prevention, an estimated 300,000 children in the U.S. have been diagnosed with juvenile arthritis (JA) and other childhood rheumatic conditions. It’s likely that many more kids are affected by rheumatic diseases and don’t even know it.
We are boldly leading the fight for families living with this mysterious disease. To help them cope, we now offer a unique package of support for young patients and their families.
The daily struggles of a child with juvenile arthritis (JA) can be heart-wrenching and frightening. Painful and debilitating flares, infusions and injections, teasing and bullying.
In the United States, about 300,000 children have arthritis, and we at the Arthritis Foundation are committed to bringing awareness to this group of diseases and the struggles of families living with the disease during July – JA Awareness month – and all year long.
Each year at this time, we commemorate the estimated 300,000 children and their families in the United States who face the everyday challenges of living with juvenile arthritis (JA) and related diseases. Juvenile arthritis is an umbrella term used to describe the many autoimmune and inflammatory conditions or pediatric rheumatic diseases that can develop in children and teens.
The various types of juvenile arthritis share many common symptoms, like pain, joint swelling, redness and warmth, but each type of JA is distinct and has its own unique characteristics and how it affects the body. Continue reading July Is National Juvenile Arthritis Awareness Month