Meet Evelyn, Gabby and Zoey. Diagnosed with achondroplasia and patients of Nemours, these strong little girls were all smiles when they reconnected
at a Little People of America Regional Conference, hosted by the Nemours skeletal dysplasia team.
At Nemours, we partner with families every step of the way to build lasting relationships. To understand the unique needs of each child—not just the condition.
And to provide the most advanced quality of care from world-renowned orthopedic and genetic experts. It’s all part of our promise to help kids everywhere have
a better chance of growing up healthy and happy.
Your child. Our promise.
©2017. Nemours Foundation. ® Nemours is a registered trademark of The Nemours Foundation.
Nemours International Medicine Program:
Expedited appointments with a specialist are available.
+1 (302) 651-4993 (Monday–Friday, 8 a.m. to 5 p.m. EST)
to help kids around the
world grow up healthy.