The Giving G

“SJIA: It’s Not Just Arthritis”

Raise funds for the Systemic Juvenile Idiopathic Arthritis Foundation. Their focus is “finding better treatments and a cure for all SJIA patients, with a special focus on patients who are refractory to current biologics.”

Goal One

Goal Two

Support families of children with SJIA in need of necessary funds to receive treatment, transportation, and more during hospital stays and after discharge at hospitals in the state of Ohio.

Support families and children with SJIA during hospital stays as well as outpatient treatment centers in the State of Ohio, by brightening a child’s day with books, toys, and a toiletry bag. We aim to provide moments of comfort and happiness during an already difficult time.

Goal Three

Close-up of a baby's neck with sjia rash.

What is Systemic Juvenile Idiopathic Arthritis?

According to the Arthritis Foundation:

“Juvenile idiopathic arthritis (JIA) is the most common type of arthritis in kids and teens. About 10% to 20% of children with JIA have a rare and serious subtype called systemic juvenile idiopathic arthritis (SJIA) causing body-wide inflammation. “Systemic” means it may affect not only the joints but other parts of the body, including the liver, lungs and heart.

SJIA, sometimes referred to as Still’s disease, can occur any time during childhood, but it most commonly starts at about two years of age. Boys and girls are equally affected. SJIA also differs from other subtypes in that it’s the only one considered an autoinflammatory rather than autoimmune disease.

SJIA is a very serious, and in some cases, life threatening disease. SJIA is more severe and can be more challenging to diagnose and treat than other types of juvenile idiopathic arthritis. Diagnosis is not done by a singular test. It must be done by a process of elimination as well as looking at the patient as a whole rather than just one symptom. It is a lifelong disease for many patients and can continue into adulthood. Treatment works for some but not all children.”