#KidsCantWait: Ziyaad's Journey The First Signs Ziyaad was born on January 2, 2017, and he is now 8 years old. He has 2 older siblings, a sister, Nureen age 18, and a brother Fayaaz, age 16. He also has a cat, named Leo. Ziyaad enjoys being outdoors, swimming, [...]
#KidsCantWait: Laila's Journey The Start of Our Journey Laila’s journey started when she was just six years old. She began complaining of leg pain, something that many parents might chalk up to growing pains. We thought, like most parents, that it was just a phase—something that would pass [...]
#KidsCantWait: Levi's + Tallon's Journeys My name is Grace Todd and I have two sons both with different forms of Juvenile Idiopathic Arthritis (JIA). My youngest Levi just turned 7, and my oldest Tallon is 10. I live in Whitehorse YT and have been fighting for them for almost a year before we [...]
Paige’s Journey with Juvenile Idiopathic Arthritis To have a chronic illness is to be fighting every day for the next. My name is Paige Simpson. I am 17 years old, I was diagnosed with Juvenile Idiopathic Arthritis, otherwise known as JIA. I have been treated for JIA for 15 years but have [...]
"I am hoping our daughter will be able to meet other girls her age with arthritis." "Willing to do anything to learn more about JIA." "We are hoping to connect with other families that have been through the hard time of arthritis and are trying to have a normal childhood for their child." "Oh [...]
Day 1 Under clear skies and magnificent views of the Lake Louise Glacier an intrepid group of riders representing Canada, Germany, Italy, Mexico and The Netherlands started the 2019 UCAN Ride4Kids. Attendants to the Childhood Arthritis and Beyond Conference enthusiastically bid farewell to the riders and after an inspiring speech by David Porte, Chairman [...]
Last month, Cassie and Friends' Juvenile Arthritis at School Puppet Show hit the road to bring juvenile arthritis education to the Okanagan! The special puppet show, which was offered free-of-charge to schools by Cassie and Friends with support from a $10,000 grant from the Telus Friendly Futures Foundation, tells the story of Cassie - a [...]
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 and they [...]
For those of us who live each day affected by juvenile arthritis or another rheumatic disease, it can often feel like there is no one who can understand what we are going through. Although this can feel isolating, when we share our juvenile arthritis and other rheumatic disease stories with one another they show [...]
Our annual Family Day conference for Juvenile Arthritis and other rheumatic diseases is in JUST ONE WEEK - and we can't wait! On Saturday, October 13th, we'll welcome over 370 kids, families and friends for a life-changing day of connection, learning and fun at the Delta Burnaby Conference Centre in Burnaby, BC. Family Day Camp [...]
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