The Love Like Crazy Foundation
celebrates and remembers the life of
Bennett Jantz Hanneman

For nearly three years, Bennett valiantly fought Pearson Syndrome, an extremely rare mitochondrial disease that affects multiple systems in the body. Despite all her endured, Bennett was a vibrant, happy boy. His smile and laughter were contagious. His bravery and resiliency were endless. Everyday, he love and was loved like crazy.

The Love Like Crazy Foundation exists to show love in tangible ways to children and their families as they fight various medical challenges and to enhance and expand education and resources to the community regarding pediatric mitochondrial disease, especially Pearson Syndrome, as well as other complex illnesses.

Simply put, the Love Like Crazy Foundation has three goals:
Loving Families
Sharing Knowledge
Supporting Research