SINGAPORE: In a poignant situation that has captured the hearts of many, two-and-a-half-year-old Jealene Caleisha Tanjaya is currently receiving treatment at the National University Hospital (NUH) after being diagnosed with a rare and aggressive form of blood cancer known as Juvenile Myelomonocytic Leukemia. This extraordinary illness affects just 1 in every 1 million children worldwide, making Jealene's case particularly unique and alarming.

Jealene's mother, Melisa, describes her daughter as a "good, strong, and cheerful girl" who continues to smile even in the face of adversity. “We never suspected that deadly cancer cells were lurking inside her little body,” Melisa shared while urging the community for financial support to help cover the exorbitant costs of treatment.

The concerning signs of Jealene's illness started appearing late in 2023 when her parents noticed red spots developing on her face each time she cried. Initially dismissed by doctors in Surabaya, Indonesia, as potential allergy reactions or harmless skin conditions, the situation escalated, prompting her family to opt for a comprehensive blood test on April 1, 2024. The shocking diagnosis of leukemia came soon after, indicated by alarming levels of white blood cells and low platelet counts.

Seeking specialized care, her parents brought her to NUH, where medical professionals confirmed the dire need for chemotherapy and a hematopoietic stem cell transplant (HSCT) within the next three months. The estimated cost of these procedures is a staggering S$330,000, a financial burden that has led Melisa to launch a crowdfunding appeal on Give.Asia. She expressed that “every single contribution will be a ray of hope” for their family in this tumultuous time, emphasizing that sharing Jealene’s story can make a significant difference.

As of the latest updates, Jealene has raised approximately S$140,700. She is set to begin her 10th cycle of chemotherapy on November 19, which will extend over a five-day duration. Thereafter, on December 5, she is scheduled for a bone marrow transplant, for which her father will act as the donor.

Melisa concluded her heartfelt appeal by asking for prayers and continued support as they navigate this challenging journey. Jealene's story is not just one of illness; it showcases the strength of family bonds and community support in the face of unimaginable challenges.

The family and supporters are urging everyone to keep Jealene in their thoughts as they fight for her recovery and hope for a brighter future.