Eight-year-old Monique Fuller was recently diagnosed with a rare form of cancer after her Covid-like symptoms rapidly deteriorated. Monique, who had never been seriously ill before, started experiencing pallor and blurred vision, prompting her mum, Chantelle Quinn, to rush her to the hospital. After a series of tests, it was revealed that Monique was suffering from acute lymphoblastic leukaemia (ALL).
ALL is a type of cancer that affects the blood and bone marrow, characterized by an overabundance of immature white blood cells called leukaemic blasts. These abnormal cells can spread to various organs in the body, including the lymph nodes, spleen, liver, and central nervous system. Monique, who had previously tested positive for Covid, experienced worsening symptoms culminating in vision issues before her admission to Westmead Children’s Hospital in Western Sydney.
Her mother, Chantelle, expressed deep sorrow at the diagnosis, stating, “I felt horrible. I lost it and broke down. I couldn’t accept it and I still have trouble accepting it… I wish I could take it from her. She’s my baby.” Since her hospitalization, Monique has begun intensive chemotherapy as part of her treatment plan for ALL.
With only around 300 individuals diagnosed with ALL in Australia last year, Monique’s case highlights the importance of early detection and treatment of rare cancers. The sudden turn of events has left the family reeling, with Chantelle also caring for Monique’s younger brother, Eli, amid the challenging circumstances.
A fundraising page has been set up to support Monique and her family as they navigate through this difficult journey of battling cancer. The community has rallied around them, offering support and well-wishes for Monique’s recovery. Despite the tough road ahead, the Fuller family remains hopeful and determined to fight against this rare form of cancer.
In conclusion, Monique’s story serves as a poignant reminder of the unpredictable nature of health and the resilience of families facing unexpected challenges. It underscores the importance of continued research and support for individuals battling rare diseases like acute lymphoblastic leukaemia.
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