• "I haven't seen this pure joy on her face in ages

    -SJIA Parent after receiving a care package

  • "What you've done has helped so much, I can't thank you enough."

    —SJIA Parent after recieving Financial Support

  • " We love The Giving G! They have provided support for our family during our daughters SJIA journey"

    -SJIA Parent after Bone Marrow Transplant

  • "The Giving G has been so supportive through our childs BMT Journey

    —SJIA Parent after Financial Assistance

OVER $65,000 RAISED

FOR CHILDREN WITH SJIA.

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 auto-inflammatory 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.”

Close-up of a baby's face with sjia rash and redness on cheeks and head.
Close-up of a baby's neck with sjia rash.
A swollen joint caused by sjia.
Baby with sjia rash.

Symptoms of SJIA include:

  • Extremely painful, swollen or stiff joints

  • Reduced joint mobility

  • Eye inflammation

  • Fatigue

  • Decreased appetite/poor weight gain

  • Slow growth

  • High Fever

  • Swollen lymph-nodes

  • Skin rash

Treatment options for SJIA:

  • Non-steroidal anti-inflammatory drugs (NSAIDs)

  • Slow-acting anti-inflammatory drugs

  • Corticosteroids

  • Biological agents

  • Experimental or investigational agents

HOW DO WE FILL OUR CUP?

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

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 United States of America.

Support families and children with SJIA during hospital stays as well as outpatient treatment centers across the USA 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.

Where can you find us?

Make a Donation

Every act of generosity—big or small—helps a family whose child is suffering from SJIA.

3% Cover the Fee