Samantha lives with osteogenesis imperfecta, a rare genetic condition that makes bones extremely fragile and prone to fractures. Her diagnosis carries special significance as she represents the third generation in her family affected by this condition, creating a unique multigenerational bond with LuskinOIC—her mother was also treated here years ago, demonstrating the lasting relationships our institute builds with families.

While Samantha previously had the ability to walk, she currently navigates her world by crawling as her condition has progressed. However, her story is far from over. Under the expert guidance of Dr. Bowen and our specialized team, Samantha is preparing for upcoming surgery combined with bone-strengthening treatments designed specifically for her unique needs.

The goal is clear and hopeful: to help Samantha walk again. Her treatment plan represents the cutting-edge care LuskinOIC provides for complex genetic conditions, combining surgical expertise with comprehensive bone health management.

Samantha’s journey highlights not only the specialized care we provide for rare conditions like osteogenesis imperfecta, but also the deep, generational trust families place in LuskinOIC. Her story continues to unfold, with each step forward bringing hope for renewed mobility and independence.

Samantha’s mom, a former LuskinOIC patient