Millie DeClercq lost her life to a rare pediatric cancer at only 6 months old

Millie DeClercq lived only six months, but her short life left a lasting impact. Diagnosed with a rare pediatric cancer before she could crawl or speak, she spent her days in hospital rooms surrounded by specialists and uncertainty. Her family described her simply as “a beautiful little girl.” When she passed, the silence that followed felt unbearable.

Cancer in infants is incredibly rare, forcing parents to learn diagnoses they’ve never heard and make impossible decisions overnight. Millie’s parents balanced hospital treatments with everyday moments—feeding, holding and comforting their daughter. Through fear and chaos, one truth stayed constant: she was loved deeply, not defined by her illness.

After Millie’s passing, her parents faced the painful question of how to move forward. Rather than being swallowed by grief, they transformed it into purpose. They built a foundation in her name to support other families facing childhood cancer—offering emotional care, financial help and a community that understands the struggle.

Because pediatric cancers are so rare, they often receive little research or attention. Millie’s foundation brings light to what many families endure quietly. Her story raises awareness and ensures that parents facing similar diagnoses don’t feel isolated, overwhelmed or forgotten.

Today, Millie’s legacy continues to grow. She never spoke a word, yet her name speaks for thousands. Her story inspires support, comfort and hope for families living through their worst moments. Millie DeClercq will always be remembered not just for her brief life, but for the purpose, compassion and strength her memory continues to inspire.