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Help Hope Live for Adeline Casson

On January 17, 2020, Adeline Beatrice came into the world. It wasn’t the birth we expected, and none of us were prepared for how this little girl would change our lives forever.

Addie was born with a rare and severe form of Osteo-Imperfecta, also known as O.I. This genetic disorder means that the child is born with soft bones that break very easily and frequently. There is no cure for this currently, and because it is so rare, the research is limited. The months after her birth were a learning experience for all of us, but especially her parents, Steven and Kate–knowing that any small or sudden movement, even something as small as a sneeze, could break one or several of her bones. For awhile, only her parents were able to pick her up, as we were all navigating the fragility of her bones. We would watch over her wondering if she would ever be able to hold her head up, to paint, or enjoy playing with her two older sisters.

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Guestbook

April 10, 2025

Proud of you!

Mirtha Miranda

April 7, 2025

You're amazing and Adeline is a little superhero ❤️
xxx

natalie arnett

April 7, 2025

Go Addie! Go Casson! <3

Cecilia Hagan