Help Abigail raise money

My name is Abby :) In November 2024, I was diagnosed with sJIA. In October 2024, I experienced fevers and joint pain almost every night for six consecutive weeks. After visiting several doctors and enduring a few hospital visits, I was referred to a pediatrician. While awaiting results over the weekend, I had to be admitted to BC Children's Hospital with a 39.8°C fever. After spending hours in the ER, they decided to admit me. Once admitted, my test results were expedited. After two days, the doctors confirmed that I had systemic juvenile arthritis. I was placed on a biologic treatment via IV, which required bi-weekly trips to the hospital. After my third visit, I went into anaphylactic shock—not from the IV treatment designed to help me, but from something else. Since then, I have not resumed the IV treatment, and I was waiting for an appointment with the allergist. Fortunately, my blood results have improved without the IV treatment, which feels miraculous. Although my blood results are not where they need to be, I am symptom-free. Today, I am living a normal life with daily oral medication and frequent follow-up visits with the rheumatologists. I feel blessed to have the support of family, friends, loved ones, and especially the medical team at BC Children's. I am running to raise awareness about this disease because I have witnessed its impact on families, regardless of how minor or severe their experiences may be. With increased funding and research, I hope to provide more families with solutions and awareness about this disease. I know it affects not just the kids but also the loved ones around us.