Four-year-old Emily Borg has always been a bright and funny girl, known for her “sassy” demeanor and love of being active with her two puppies. However, when she suddenly lost her appetite and stopped acting like herself, her parents knew something was wrong. Initially diagnosed with a virus, the family later learned in March that Emily had stage 4 high-risk neuroblastoma, a rare childhood cancer. Despite being dismissed by doctors multiple times, Emily’s mother’s intuition led her to push for further tests, which confirmed the diagnosis. Since then, Emily has undergone surgery and multiple rounds of chemotherapy to remove the tumor. The family received promising news in June that the cancer had been shrunk to a contained, single location, but there is still a long road ahead. Emily is now preparing for a bone marrow transplant as part of her intensive treatment plan. The family is fundraising for a vaccine developed in New York that could help in the event of a relapse. Despite the challenges, Emily remains determined and her family is inspired by her spirit. They are grateful for the support they have received from the community.
Young Queensland girl Emily facing the challenges of rare cancer neuroblastoma
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