Medication

For most of my life, I’ve had Morphea. Starting as a red mark on my chin as ayoung child, it eventually turned darker and over the years, spread to areas onmy forehead, and neck. Morphea, also known as localized Scleroderma, is an auto immune disease thatcauses hardened and darkened patches…

Bella is turning 7 this year and while most kids her age are focused on playing outside and colouring, Bella is dealing with the ups and downs of Muckle-Wells Syndrome which includes painful injections. As you can imagine, she has been struggling with the large doses of anakinra and the…

Meet Lily. One morning, at the young age of 2, our daughter Lily woke up limping and her left knee looked slightly swollen. She didn’t seem to show that she was in pain, but was refraining from putting weight on her left leg. We had no idea what happened and didn’t…

“If you told me a few years ago that I would be pursuing my dream of playing post-secondary volleyball at Dalhousie University, I would have laughed out loud because at the time it seemed near to impossible.” Meet Ella. In April of 2020, I was diagnosed with a rheumatic condition…

Make lemonade! At least that’s what Jacob Shiell did when he was diagnosed with Systemic Idiopathic Juvenile Arthritis (SJIA) on his eighth birthday in October 2021.  Jacob’s journey began with unexplained foot pain and swelling. Over the next few weeks, the pain and swelling worsened and spread to his right…

We have been asking youth with rheumatic disease to share their story! Sharing stories helps build community and connections. We hope that Jenna’s amazing story inspires you to share your own story.  My name is Jenna Kedy. I am 18 years old and live in Halifax, Nova Scotia.  As a…

Caden was diagnosed with JIA when she was just 3 years old. When we first noticed her limping, we thought she may have hurt her knee skiing as we had just taken her for her first lessons. Then one morning I saw her sneaking down the stairs from her bedroom,…

This article was written and reviewed by the Cassie + Friends Medical Advisory Committee made up of Dr. Roberta Berard (London Health Sciences Centre), Dr. Nadia Luca (Alberta Children’s Hospital) and Dr. Lori Tucker (BC Children’s Hospital). To learn more about the Cassie + Friends Medical Advisory Committee, click here. Some…

Written by young adult JIA patient, Julie Beausoleil, this blog post was originally published by www.takeapaincheck.ca on June 29th, 2021. Take A Pain Check is a juvenile arthritis focussed podcast hosted by 18 year old Natasha Trehan, that provides a recognizable platform for youth and young adults to share their experience with…

“Every furrow of her brow makes me want to stop” If you have ever struggled to give your child an injection or to manage your child’s – or your own – emotions about their treatments, you are not alone!  In the lead up to our Methotrexate session, we talked with Yvonne…

My daughter Elena was diagnosed with Juvenile Arthritis at age 2. Arthritis? That was an elderly person’s disease, I thought. I had no idea the depth of the disease or what would lie ahead for us. First, she started with redness and swelling in her knees. I took her into the doctor…

Teens Taking Charge: Andrea’s JIA After being diagnosed with Juvenile Arthritis at the age of two, Andrea’s childhood and teen years were much different than those of her peers. Her experiences with doctors’ visits and medications from such a young age forced her to mature faster and understand things her…