Proceeds from the Swamp Pop Music Festival benefit the Cystic Fibrosis Foundation.
The mission of the Cystic Fibrosis Foundation is to cure cystic fibrosis and to provide all people with the disease the opportunity to lead full, productive lives by funding research and drug development, promoting individualized treatment, and ensuring access to high-quality, specialized care.
Cystic fibrosis (CF) is a life-threatening genetic disease that occurs when a child inherits two copies of the defective CF gene – one from each parent. More than 10 million Americans (one in 31 people) are symptomless carriers of the gene. Each time two carriers conceive, there is a 25 percent chance their child will have CF.
The defective CF gene causes the body to produce an abnormally thick, sticky mucus that clogs the airways and leads to life-threatening lung infections. The thick CF mucus also obstructs the pancreas, preventing enzymes from reaching the intestines to digest food.
There are approximately 30,000 children and adults in the United States who have CF.
When the Foundation was established in 1955, children with CF rarely lived long enough to attend elementary school. Due in large part to the Foundation’s aggressive investments in innovative research and comprehensive care, many people with the disease can now expect to live into their 30s, 40s and beyond.
The CF Foundation funds and accredits a national care center network — including Tulane University Medical Center in New Orleans and LSU Medical Center in Shreveport — that has been recognized by the National Institutes of Health as a model of care for a chronic disease.
The Cystic Fibrosis Foundation is one of the most efficient organizations of its kind and is an accredited charity of the Better Business Bureau’s Wise Giving Alliance.
You can help us add tomorrows every day for CF patients. Click here to DONATE to the Swamp Pop Music Festival and CF Foundation.
Click here to learn more about the CF Foundation.
2016 Festival Sponsors:
Title Sponsor Price LeBlanc Toyota & Nissan
Fais Do Do Sponsor
Volunteer T-Shirt Sponsor
Lagniappe Sponsor .
Friend of the Festival Sponsor
To discuss sponsorship and donation opportunities, contact our office at (225) 769-9994 or e-mail at email@example.com
Brad Brewster, Court Batson, and Thomas Peri of Bent Media and Mystic Knights of Mau Mau generously donated their expertise and many, many hours of time to the CF Foundation to develop our festival website.
Illustrator Mark Andresen developed “Kenny,” our musical alligator logo as a donation to the CF Foundation.
Shane K. Bernard, Historian of McIlhenny Co. and author of “Swamp Pop: Cajun and Creole Rhythm & Blues” and “The Cajuns: Americanization of a People” both available from University Press of Mississippi, advised festival staff.
Todd Long generously donates his time and skill to emcee our Jambalaya Cook-off.
To donate to the Swamp Pop Music Festival and the CF Foundation, mail your tax-deductible check made out to the Cystic Fibrosis Foundation (please write “SPOP” on the Memo line) to:
Cystic Fibrosis Foundation – Baton Rouge Office
10532 S. Glenstone Suite C
Baton Rouge, LA 70810
To discuss your donation or other ways you’d like to help or to donate using a credit card, contact us at:
phone: (225) 769-9994
toll-free: (877) 753-9990
To donate your car, call 1-800-456-5517 or link to the
CF Foundation Vehicle Donation website.
THANK YOU for your generosity. We come closer to a cure every day and with your help, we can make CF stand for “Cure Found.”
Sarah Eastridge, a beautiful, young lady, was the inspiration for the founding of the festival.
She was diagnosed with CF as a baby. Since then she has been hospitalized numerous times, has had many surgeries, and numerous tests, scans, and procedures that required anesthesia. Her IV treatments have become very extensive because she has developed another problem with her lungs. Although she has had many difficulties with digestion and being able to gain and maintain her weight, she is as healthy as can be expected. It requires a lot of extra care to keep her this way.
Twice a day she has to have breathing treatments and vest therapy. She realizes that the treatments are what enable her to breath easier. The vest therapy is a new way of getting the mucus to dislodge in her lungs instead of the pounding her parents use to have to do. She does a breathing treatment daily called Pulmozyme. She also has to do TOBI breathing treatments twice a day every other month.
Several times a month Sarah goes to Tulane Medical Center in New Orleans to meet with her doctors. She has severe stomach problems. She also has lung problems that are progressively getting worse due to her new diagnosis of Atypical Mycobacterium Disease. She is somewhat underweight, but her appearance can be misleading. She has had several surgeries hoping that they would help her stomach problems, but unfortunately they have not corrected the problems yet.
She loves playing with her relatives and friends. Riding 4-wheelers and playing on the computer are also high on her love-to-do list.
With continued progress through research, love, and care of her family, friends, doctors, and those who support the CF Foundation, Sarah may indeed live to see a cure. Please keep Sarah and other precious children with CF in your daily prayers. With your help, we can make CF stand for “Cure Found.”
Click here to DONATE to the Swamp Pop Music Festival and CF Foundation and help Sarah, Kayde, Libby, and other individuals with CF!