#WhyIRun - Two Sisters' Story The Story of Two Sisters Hello, my name is Queena, and I was diagnosed with Lupus and Juvenile Arthritis in 2021. During this time, it was hard to ask for help. For the most part my "illness" - or whatever was causing my swollen joints and excruciating [...]
#WhyIRun - Hope for Harley Harley is our tiny warrior. Just after turning 2, in August 2022, Harley started having difficulty walking one day out of nowhere. It pained her to tears and she had to hold onto someone to walk or be carried. She was on Amoxicillin for an ear infection, and [...]
working with rheumatic disease Knowledge is power… And what better way to feel empowered in navigating the workplace with a rheumatic disease than to understand your rights and how to advocate for them? Whether you're a teenager looking for your first job, a young adult looking for workplace advocacy or disclosure tips, or [...]
Youth Mental Health Strategy Funding Announcement NEWS RELEASE Two Canadian teams awarded new funding to study mental illness in youth with rheumatic diseases. Brain Canada and Cassie + Friends unveil the recipients of the Addressing Mental Health in Paediatric Rheumatic Diseases Team Grants program. Source: Brain Canada MONTREAL, April [...]
Alison Legge: Navigating the workplace with a rheumatic disease I was diagnosed with Juvenile Idiopathic Arthritis (JIA) at three years old. Having dealt with the disease with varying degrees of severity for the past 24 years, I can say one of the most challenging things to manage is other [...]
bridging the gap improving lives through research, education, connection, and support We're living in a time of exciting progress, where scientific breakthroughs are paving the way for better care for children and families dealing with pediatric rheumatic diseases. Every day, dedicated researchers, including those in our CREW Network, are pushing the boundaries of [...]
Reine Hodroj - Learning to Live with Behcet's Disease Living with a chronic illness is an unimaginable challenge, and Behcet's Disease has been my constant companion in this journey. This rare autoimmune condition, characterized by recurrent oral and genital ulcers, skin lesions, and systemic inflammation, has disrupted my life in many ways. However, my [...]
Bella is turning 7 this year and while most kids her age are focused on playing outside and colouring, Bella is dealing with the ups and downs of Muckle-Wells Syndrome which includes painful injections. As you can imagine, she has been struggling with the large doses of anakinra and the needle pokes. To [...]
I graduated from the University of British Columbia in 2022 with a Bachelor of Science in Biology, with a focus in Genetics and Evolution. Shortly after graduating and working in a laboratory, I came to the realization I can make a bigger impact in healthcare and biotechnology by leveraging my scientific expertise to [...]
My name is Kayla, I am 25 years old and have lived with arthritis for over half my life. I attended Pain Education Day at the International Symposium for Pediatric Pain last month, and it was not what I initially expected. I didn't realize I would have the opportunity to meet so many other [...]
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