The Kennedy Ladd Foundation, Inc.

The Ladd Family is on a mission to raise Awareness because with awareness comes a cure!

Kennedy and Lincoln Ladd are 1 in 100,000 with a diagnosis of MPS 1-Hurler Syndrome.

MPS I-Hurler is a rare, life-threatening disease, evolving in multisystem morbidity including progressive neurological disease, upper airway obstruction, skeletal deformity and cardiomyopathy. 

There is currently no cure for MPS.
Out of adversity the Ladd Family formed The Kennedy Ladd Foundation, Inc. 

The Kennedy Ladd Foundation, Inc. is an approved 501(c)3 on a mission to fund research for a cure. While funding research the foundation provides iPads to Hurler patients going into Bone Marrow Transplants.

We need your help in raising awareness.

Tell others, Wear purple, Pray, Share, educate and find their story on Facebook. 

You can find their personal journey at Kennedy and Lincoln Ladd’s Prayer Group.

Or

Visit www.kennedyladd.org