Before his diagnosis, Atlas was a happy, curious little boy with the biggest smile. His mom, Jacqueline, began noticing small changes — more fatigue, moments where he just wasn’t himself. That quiet feeling that something wasn’t right continued to grow.

After countless tests and appointments, Atlas was diagnosed with high-risk metastatic neuroblastoma (stage M) with an ALK mutation. From that moment on, life shifted to hospital rooms, scans, surgeries, and oncology care. Atlas has already undergone major surgery to remove part of his tumor and continues to face intensive treatments, with more still ahead.

Atlas is very young and has already spent more time in hospitals than any child ever should. His care requires frequent appointments, long hospital stays, and constant monitoring. One parent has had to step away from work to be present for his treatment, creating added financial strain on top of ongoing medical and travel expenses.

Despite everything he has endured, Atlas remains gentle, trusting, and full of light. His smile still shines through even on the hardest days — a reflection of his incredible strength and resilience.

Jacqueline shared what support from the Millie Moo Foundation has meant to their family:

“Support like this grant means more than financial help. It reminds me that Atlas is seen, that our family is not alone, and that kindness still exists even in the darkest seasons. Thank you for walking beside us and for helping carry some of the weight during this journey.”