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, taking each step on [...]
Hello, My name is Emma Linsley, and I am from Saskatoon, Saskatchewan. When I was 15 years old, I was diagnosed with JIA. Along with needing to learn to manage the physical ailments of the disease, this diagnosis brought with it a complex set of other challenges that my support network and I would [...]
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 arthritis in addition [...]
The Beginning As a toddler learning to walk, Audrey caught on pretty fast. By her 1st birthday she was already zooming around with impressive coordination and balance. When we noticed that she was limping on-and-off at 18 months of age, we knew something was up. Her right ankle was swollen so we decided to [...]
Hi, my name is Savannah and I am a second-year university student studying kinesiology and living in Windsor, Ontario. I was diagnosed in grade school with Juvenile Idiopathic Arthritis (JIA). A while ago, a member of my care team suggested I google Cassie + Friends to learn about the programs and resources offered for [...]
Macrophage Activation Syndrome (MAS) is severe inflammation of the immune system which can be associated with rheumatologic conditions such as Juvenile Idiopathic Arthritis (JIA). I was diagnosed with both conditions in October 2010. My name is Gauri Raj and I am currently 21 years old. When I was 10 years old, I had lost [...]
I am the proud mother to a vibrant 3.5-year-old, Émilie, who was diagnosed with Juvenile Idiopathic Arthritis (JIA) shortly before her second birthday. We were fortunate as a family to receive a diagnosis in a relatively rapid timeframe thanks to knowledge about navigating the health care system (I work as a nurse) and a [...]
Parenting is joyful, frustrating, rewarding and exhausting. Parenting a child with a chronic disease gives you a double dose of it all; you face challenges most parents never dream of. You juggle doctors, therapists, hospitals, insurance companies, pharmacies and the list goes on. Then there are the emotional and behavioural issues you deal with. [...]
My name is Maryse Hendi, I am 18 years old, and I was diagnosed with Systemic Lupus Erythematosus (SLE) when I was 10 years old. What is SLE? More commonly known as Lupus, it is a disease in which the immune system is hyperactive and not only attacks disease-causing pathogens, but also the normal, [...]
Meet Oliver! A vibrant young boy with autoinflammatory disease living in Williams Lake, BC! Oliver has always been the type of child that brings joy to everyone around him. We couldn’t go to the grocery store without the smiling baby drawing everyone near. His first year of life was good. He was a perfectly [...]
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