My Story…
My name is Abby :) In November 2024, I was diagnosed with sJIA. In October 2024, I had fevers and joint pains almost every night for six weeks straight. After seeing doctor after doctor and with a few hospital visits, I was referred to a pediatrician. While waiting for results over the weekend, I had to be admitted to BC Children's Hospital with a 39.8 fever. After being in the ER for hours, they decided to admit me. Once admitted, I was able to have my test results expedited. After two days, the doctors determined that I had systemic juvenile arthritis. I was put on a biologic treatment through IV and that required bi-weekly visits to the hospital. After my third visit, I went into anaphylactic shock, not from the IV treatment to make me better, but something else. Since then, I have not been on the IV treatment and am waiting for an appointment with the allergist. Fortunately for me, my blood results have improved without the IV treatment and it is a miracle. Today, I am living a normal life with daily oral medication and a bi-monthly visit with the rheumatologist. I have been blessed to have support from family, friends, loved ones, and especially from the medical team at BC Childrens. I am running to bring awareness to this disease as I have seen the impact it has on families no matter how minor or severe. With more funding and research, I hope to bring more families with solutions and awareness with this disease. I know it affects not just the kids, but the loved ones around us.
Description
Help kids and youth with Juvenile Arthritis (JA) and rheumatic diseases see that #HopeFlares when we unite for stronger families, resilient youth and a cure!
In Canada, 3 in 1,000 kids face JA and related conditions like SJIA/Stills, lupus, fever syndromes, JDM and autoinflammatory disorders. These diseases can lead to chronic pain, disability, vision loss, mental health struggles, and even life-threatening complications—yet they remain drastically underfunded and overlooked, with only 20% awareness nationwide.
Team Cassie + Friends is Canada’s only movement 100% dedicated to the JA community. What began with one dad running in 2007 has grown into 750+ runners and thousands of donors rallying together annually for a pain-free future for kids!
By supporting our run/walk, you’ll directly support:
Groundbreaking research into precision medicine, mental health, and a cure
Vital resources like free medical equipment, financial aid, and Comfort Kits
Mentorship for youth and caregivers
Education and connection events for families
Advocacy for earlier diagnosis and equitable care
Together, we can bring hope, support, and brighter futures for kids facing lifelong challenges.
Questions? Contact Marissa Sangers at marissa@cassieandfriends.ca
If registration cost is a barrier, ask about our Kids Run Free bursary program.