Mrs. Louisiana United States 2009: Cystic Fibrosis Foundation of Louisiana Bowl for Breath

About Mrs. LA United States 2009

A proud native of Louisiana’s Cajun Country, Anne Katherine met her husband, Jackson, on the playground of their elementary school. Though not yet a parent, she has 1200 “kids” to guide, encourage, and sometimes reprimand as the Director of Student Life at a college in New Orleans. She is committed to expanding her daily work of motivating students to become active citizens and leaders through service learning and volunteerism.

Anne Katherine holds an M.Ed. in University Administration and is undertaking doctoral studies in Organizational Psychology. She serves on an education advisory board and is active in several organizations including Habitat for Humanity, Catholic Charities of Greater New Orleans, Cystic Fibrosis Foundation of Louisiana, and Kiwanis International.

When not working with students or serving her community, Anne Katherine enjoys traveling, singing in the car, guiding her Fantasy Football team to the playoffs, and spending autumn Sunday afternoons in the Superdome cheering on the Saints with her husband.

Sunday, December 6, 2009

Cystic Fibrosis Foundation of Louisiana Bowl for Breath

This weekend, I headed south to Houma for the Cystic Fibrosis Foundation of Louisiana's Bowl for Breath. Of course, my best friend, Millie, was with me, and we formed TEAM INJURY -- named mainly for back problems & Millie's shoulder issues. Neither of us had bowled in years, and we were overjoyed to take the opportunity to re-introduce ourselves to this past time, as well as yummy bowling alley food, all while supporting CFF-LA. Needless to say, we weren't winning any bowling awards; however, I will absolutely return next year to take part in this wonderful event! The people of the Houma area produce an exceptional event compete with bowling, raffles, scavenger hunts, and more! So, mark your calendar for the first Saturday in December 2010 and join us in Houma at Creole Lanes to support the Cystic Fibrosis Foundation. This is such an incredible organization, and you can learn more by visiting www.cff.org.