August 2023

C+F Inventing Room: Reinventing the Injection Experience for Kids and Families Affected by JA and other childhood rheumatic diseases in Canada

By |August 31st, 2023|Advice, Advocacy, blog, Injection, Medication, Past Events|

Inspired by the Roald Dahl Charity’s Marvellous Nurse Inventing Rooms, on August 23rd, we hosted our very own C+F Inventing Room to ask the community and together envision what our C+F Injection Coping Kits should include. With the help of medical experts, parents and youth, we dove in and got to work! We started [...]

May 2019

250 kids, families and friends set to attend first Edmonton Family Day

By |May 1st, 2019|Family Day, News|

"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 [...]

April 2019

UCAN Ride4Kids (Day 1 to 3) – Updates from the Road from Dr. Jaime Guzman

By |April 29th, 2019|Advocacy, Current Events, Research, UCAN Ride4Kids|

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 [...]

February 2019

Brick by Brick: Youth leaders build the patient experience they never had in hopes of helping others

By |February 14th, 2019|Past Events, Stories, YLN|

Author: Zoya Jiwa, YLC Program Designer and founder of As We Are Style - a blog about facing health challenges with courage and style. Last weekend, Cassie + Friends’ Youth Leadership Committee got together for our first team retreat on a surprisingly sunny afternoon (thank you, Vancouver!) with a lot of excitement and a BIG [...]

Puppet show helps BC Interior parents fight loss of children’s arthritis care

By |February 11th, 2019|Advocacy, Elementary, News, School Toolkit, Stories|

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 [...]

January 2019

Erika and Elena’s arthritis journey: Staying strong through the ups and downs

By |January 31st, 2019|Advice, Injection, Stories|

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 [...]

School Toolkit: Gym class with JIA

By |January 17th, 2019|Advice, Elementary, High School, School, School Toolkit|

For many children with JIA or other rheumatic diseases, physical challenges at school can be huge barriers, particularly when it comes to gym class. In a recent study, researchers found that 38% of kids with JIA were unable to participate in gym with their peers. Paired with misunderstanding and lack of knowledge on the [...]

November 2018

3 tips for travelling with a child with a flare

By |November 9th, 2018|Advice, Pain Tips, Stories|

As stressful and painful as experiencing a flare can already be at home, the idea of travelling with a flare may sometimes seem downright impossible. With some help however, you and your child can still enjoy taking a trip together. These are Cassie and Friends community member and mother Tanya Cassidy Irwin's three tips for [...]

Emily’s story: Navigating pain, planes and biologics

By |November 9th, 2018|Pain Tips, Stories|

Tanya Cassidy Irwin is a mother and Cassie and Friends community member from Langley, BC. This is her story of navigating pain, travel, medication and the unknown throughout her daughter Emily's journey with Oligoarticular JIA.    In September 2015 there was the most subtle of hitches in our daughter Emily's step. Within three weeks she [...]

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