Annual Report 2023-2024

This strongman can lift a 330-pound stone over his head and carry an 800-pound yoke for 50 feet. “Just because I look different doesn’t mean anyone should underestimate what my body and mind are capable of,” said Steven. Now in his early 30s, Steven has a new challenge: firefighting. “Fire may have won round one with me when I was a kid, but I’ll win round two,” he said. A rare connection Keira and Madelyn were both born with the same rare condition, congenital absence of the left arm. Both received treatment at Shriners Children’s – Keira in Philadelphia and Madelyn in St. Louis. Seven years ago, thanks to the power of social media, their mothers connected, and a special bond between the pair began. Their story is an example of how Shriners Children’s patients find much more than amazing care within our walls.

because there is genuinely an immense amount of joy in meeting someone who looks just like you, after knowing each other for years but being separated by distance,” said Madelyn. Keira said she was excited when she saw Madelyn and happy that they could meet in person. The most special part of the visit was their opportunity to speak together at Keira’s school. During the presentation, the girls shared their stories and educated students about braces and prosthetics. “Keira’s self-confidence was evident as she stood with Madelyn in front of the large group of students, something she never would have done before!” said Keira’s mom, Jessica. “Not many individuals are born completely missing their left arm, and knowing that Keira is able to see

Despite their age difference, the girls share many similarities. Keira, 8, is often described as 23-year-old Madelyn’s mini-me. Those similarities have allowed them to find someone

who can relate to their daily experiences. Over the years, the girls and their moms found support in each other through messages and video calls. The fated friends met in person at last through Shriners Children’s

and the Lucky Fin Project, an

educational resource and support network for families of children with limb differences. “Meeting Keira in person was one of those moments that was incredibly hard to put into words

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