Nashville concert event “Hope Springs” supports children with arthritis

By |May 27th, 2021|Current Events|

New hope for kids living with arthritis in BC Interior thanks to replacement specialist clearing red tape and a special live-from-Nashville concert event benefiting Canadian Children’s Charities Penticton, British Columbia, May 18, 2021 – 97 South Song Sessions, the group behind Penticton’s summer songwriters festival of the same name (97SouthSongSessions.com), will produce and donate [...]

A Call to #PrioritizePain with Cassie + Friends

By |May 14th, 2021|Advocacy|

Cassie + Friends is joining other leading pain and pain-related organizations to support the recommendations of the #CanadianPainTaskForce and call for their implementation. Over the next week, we will be sharing some of the targeted recommendations laid out in “An Action Plan for Pain in Canada” and why they are important to kids, youth [...]

Parenting a child with JIA: Fear, uncertainty, hope, and an endless list of questions

By |May 13th, 2021|Advice, JIA, Mental Health, Mental Health (Caregivers), Stories|

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 [...]

The Story Behind the Session Putting on Your Life Jacket: Self-care for Caregivers, Parenting a Child with Chronic Disease, and more!

By |May 13th, 2021|Advice, Mental Health (Caregivers), Stories|

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.  [...]

Lupus: What is it and how can you show your support this #LupusAwarenessMonth

By |April 30th, 2021|Lupus, Stories|

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, [...]

Hacking our way to a pain-free future for kids. 

By |April 29th, 2021|Advocacy, Current Events|

How can we best transform the lives of youth affected by rheumatic diseases through Cassie + Friends? This March, in recognition of juvenile arthritis awareness month and #WORDDay, we hosted the very first Cassie + Friends Hackathon to get creative and collaborative around community-driven solutions that answer the question “How can we best transform [...]

Oliver’s Diagnostic Journey: Periodic Fever Syndromes

By |April 15th, 2021|Fever Syndromes, Northern BC, Rare Disease Stories, Stories|

 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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