She weighed 8 pounds even.
She was 19 3/4 inches long.
She had an infectious smile.
She began showing symptoms of Krabbe Disease just before 3 months of age.
She wasn’t diagnosed with the disease until she was 6 months old.
She saved her brother’s life.
The high school basketball team that MK’s mom and dad coach dedicated this past season to her, and their motto was #justplayformk.
The community really rallied around her and showed an overwhelming amount of support.
Mabry Kate touched an insurmountable number of lives in a variety of ways.
She’s a super hero in a tiny body.
She has a law named after her called the Mabry Kate Webb Act that will add Krabbe Disease and other leukodystrophies to the TN Newborn Screening.
Mabry Kate passed away on February 7, 2015, but her spirit continues to live on!