Injection + Medication Support
Understanding treatment — making it manageable
Many children living with rheumatic disease require medication as part of their treatment — sometimes including injections. For families, this can feel intimidating at first.
With the right information, tools, and support, managing medications and injections becomes a routine part of care. This page provides clear guidance to help you feel more confident and prepared.
Understanding Treatment
Treatment plans vary depending on your child’s condition, but often include medications that reduce inflammation, manage symptoms, and help prevent long-term joint damage.
You may hear terms like:
- Biologics – (medications derived from living organisms—such as human, animal, or
microorganism cells—rather than through chemical synthesis) - DMARDs – (Disease-Modifying Anti-Rheumatic Drugs)
- NSAIDs – (medications used to reduce pain, lower fever, and decrease inflammation)
Your healthcare team will guide you through what each medication does and why it’s recommended for your child.
Injections — What to expect
Some medications are given by injection, either at home or in a clinical setting. This can feel overwhelming at first, but many families find that with practice and support, it becomes more manageable.
It’s okay if it takes time to adjust — both for you and your child.
“My family TRULY appreciates all you guys have done to help us through this journey!”
— Parent
Making Injections Easier
Practical tips that together can make things easier for you and your child.
- Use numbing cream or a numbing patch before injections
- Try distraction tools like vibration devices (e.g. Buzzy), fidgets, or blowing bubbles
- Create a routine so your child knows what to expect
- Offer small rewards or use a sticker chart
- Let your child have some control (choosing timing, location, or tools)
Managing Side Effects
Some medications may cause side effects such as fatigue, nausea, or irritation at the injection site. Your healthcare team will explain what to expect and how to manage these.
If you have concerns, always reach out to your child’s care team — they can help adjust treatment or provide additional support.
Common Challenges
Many families face similar challenges early on—from needle anxiety to sensory sensitivities and emotional resistance. These are natural responses as children adjust to new routines and treatments, and with the right support, they can become easier to manage over time.
Needle anxiety
- Use numbing cream or a numbing patch
- Talk openly with your child about their concerns and how to feel more relaxed
- Use a vibrating distraction tool like i.e. BuzzyBee, fidget spinners or blowing bubbles
- Create a medication sticker chart with built-in rewards
Sensory triggers (smell, environment)
- Use odourless wipes when possible
- Try scent masking (e.g. coffee)
Resistance or fear
- Keep communication open
- Give your child a sense of control
- Stay consistent with routines
Check out the Injection Support resources and webinars
When to Ask for Help
If you’re struggling with administering medication or your child is having a difficult time, reach out to your healthcare team or support network. There are always options to make things easier for you and your child.
Related Support
Finding Your Rhythm
What feels difficult at first often becomes more manageable with practice, support, and the right tools. You and your child will find a rhythm that works — and you don’t have to do it alone.
“I consider C+F to be one of the greatest supports I have received as a young person with arthritis. C+F has provided me with a community, countless opportunities, andmany resources that have helped me navigate various aspects of my life with a rheumatic disease.”
— Alejandra Van Dusen
