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Treatments
+ Medications

How treatments support your child - today and over time.

Treatment for juvenile arthritis and other childhood rheumatic diseases focuses on controlling inflammation, managing symptoms, and preventing long-term joint and organ damage.

With the right care—started early—many children can live active, full lives, and some may achieve remission.

Understanding how treatments work, and how they are used over time, can help families feel more confident navigating decisions. Care plans are tailored to each child and evolve as their needs change.

How Treatment Works

Treatment is often ongoing and changes over time.

Rheumatic diseases are typically managed using a combination of medications and supportive therapies. The goal is to control inflammation, reduce pain, maintain joint function, and support overall wellbeing. Treatment may include medications such as NSAIDs, methotrexate, biologics, corticosteroids, and supportive therapies.

Treatment is often ongoing and may be adjusted over time. Regular monitoring helps ensure medications are effective and that any side effects are managed appropriately.

It can take time to find the treatment approach that works best for each child, and adjustments along the way are common.

Medication Types

Different medications play different roles in treatment.

NSAIDs (Non-Steroidal 
Anti-Inflammatory Drugs)

Often used to reduce inflammation and relieve pain. These may be one of the first treatments introduced.

DMARDs (Disease-Modifying 
Anti-Rheumatic Drugs)

Used to slow disease progression and control inflammation over time. Methotrexate is a commonly used example.

Biologics

Target specific parts of the immune system to reduce inflammation. These are often used when other treatments are not sufficient.

Corticosteroids

Used to quickly reduce inflammation during flare-ups or severe symptoms. Typically used for shorter periods.

Treatment Plans

How individualized treatment plans are developed for youth.

Treatment plans for juvenile arthritis (JIA) and other childhood rheumatic diseases are tailored to each child based on factors such as:

  • Type and severity of the condition
  • Number of joints affected
  • Presence of systemic symptoms (such as fever or fatigue)
  • Response to previous treatments
  • Overall health, development, and daily life

Pediatric rheumatology teams work closely with children and their families to adjust treatment plans over time—ensuring care keeps pace with a child’s needs as they grow.

Monitoring and Follow-up

Ongoing monitoring is an important part of treatment. This may include regular appointments, blood tests, and assessments to ensure that medications are working effectively and safely.

Adjustments to treatment are common and help ensure the best possible outcomes.

Side Effects

You don’t have to manage side effects by yourself.

Like all medications, treatments for rheumatic disease may have side effects. These vary depending on the medication and the individual.

Common considerations may include:

  • Fatigue or nausea
  • Injection site reactions
  • Increased risk of infection (for some medications)

Healthcare providers will explain what to watch for and how to manage side effects.

Supporting Treatment

Supporting treatment beyond medication

Medication is only one part of treatment. Physical activity, nutrition, sleep, school support, and mental health care can all play an important role in helping children manage symptoms and maintain overall wellbeing.

A balanced approach helps support both short-term comfort and long-term health.

Families often have questions about medications, side effects, injections, and long-term treatment decisions. Explore our FAQs, videos, and support resources below.

Treatment FAQs

Treatment Questions about medications + treatments

These frequently asked questions about methotrexate, biologics, and treatment for pediatric rheumatic diseases were developed with guidance from the Cassie + Friends Medical Advisory Committee and JA young adult patient Julie Beausoleil.

Questions from families and caregivers answered by pediatric rheumatology experts.

Do you have more questions?

Contact Us

Related Support

Explore related support to better understand treatment and manage symptoms.

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Treatment as part of a broader care plan

Support for the whole family—at every stage.

Treatment is only one part of the journey. Children and families often need support beyond medications—from understanding the condition, to managing school and daily life, to navigating emotional and mental health challenges.

With the right care and support, many children and youth living with juvenile arthritis and other rheumatic diseases can stay active, build confidence, and live full lives.

Cassie + Friends is here to support not just the child—but the entire family—with trusted resources, connection, and guidance at every stage.