June 2023

Tough as Nails: A Father Reflects on his Two Daughters and Childhood Rheumatic Disease

By |June 5th, 2023|Advocacy, High School, JIA, Post- Secondary, Rare Disease, Stories, TMJ|

"We're very proud of our girls for showing the fortitude needed to not let these diseases define them." Hello families! My name is Mike Wiens, husband to Jesica and father to two girls, Vanessa 24 yrs old, and Sarah 23 yrs old. We're happy to call Port Moody, BC our home since relocating here [...]

May 2023

Mental Health Matters: Kaese’s Journey With JA

By |May 5th, 2023|Advocacy, JIA, Mental Health, Mental Health (For Youth), Stories|

"Feelings and emotions are real, and should be felt and openly discussed." Meet Kaese and his mom, Jennifer. Together, they have chosen to share their story of being diagnosed with JIA and the many impacts that can have on a child and family's mental health. To read more Cassie + Friends' Youth Mental [...]

March 2023

Other Ways You Can Help

By |March 9th, 2023|

More Fun Ways To Get Involved Cassie + Friends relies on our community to help take initiative in spreading awareness about juvenile arthritis and other rheumatic diseases by leading new and fun fundraisers. There are so many easy ways to get involved such as creating a birthday fundraiser on Facebook or a starting your [...]

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August 2022

What Canadian Juvenile Arthritis Families Think About Telemedicine in COVID-19

By |August 20th, 2022|Advocacy, COVID, CREW, Current Events, Research|

Canadian Pediatric Rheumatology Families in the Spotlight! We want to thank every parent and youth who participated in our survey to find out more about Canadian families' preferences and experiences with Telemedicine practices during COVID-19. Your results have been published as a scientific research paper - here's our summary below and a link to [...]

March 2022

Take Action: 5 Simple Ways to Recognize Juvenile Arthritis Month

By |March 3rd, 2022|About JIA, Advocacy, Current Events, JIA, YLN|

It's #JuvenileArthritisAwarenessMonth, what can I do to help? To make it easy for you to get involved, we've put together 5 Simple Ways to Recognize Juvenile Arthritis Awareness Month. From educating classmates to participating in fundraising events (such as our Cassie + Friends Run/Walk for Juvenile Arthritis- check out #1), we have the opportunity [...]

How to #MakeMarchCount this Juvenile Arthritis Awareness Month

By |March 1st, 2022|About JIA, Advocacy, Current Events|

A message from our Board Chair, David Porte. Dear Cassie + Friends Community, Today is the start of Juvenile Arthritis Awareness Month and I am writing to invite you to get behind our mission by becoming a monthly donor to Cassie + Friends. Even just $10, $20 or $50 dollars per month can make a big [...]

November 2021

Will you join Jeremy as part of our CREW?

By |November 24th, 2021|Advocacy, Calgary, CREW, JIA, Scotiabank Charity Challenge|

There are lots of ways to show your support for the Juvenile Arthritis community on #GivingTuesday - like, share, educate and, of course, donate. To get inspired, we thought you might like to meet Jeremy from our Calgary CREW. On Nov 30th, we hope you'll join Jeremy and our CREW of parents/friends all across [...]

September 2021

Medical Advisory Committee: Biosimilars

By |September 1st, 2021|Advocacy, Current Events, Medication|

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 youth and families may [...]

August 2021

Arthritis Awareness Month: Let’s Make Juvenile Arthritis a National Priority.

By |August 30th, 2021|Advocacy, Current Events, News|

6.5 million people are affected by arthritis in Canada and about 24,000 of them are children. Cassie + Friends is just for them. Kids like Audrey (pictured right) - diagnosed at just 18 months - need our help to make sure their health and futures are a priority, even beyond the dedicated care from [...]

From Clips to Cause: How one Windsor youth is giving back to the rheumatic disease community.

By |August 12th, 2021|Advocacy, JIA, London, Stories|

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 [...]

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