SAVE THE DATE!

Bellydance Challenge
click for info!

Sunday, August 2
7:00 PM
at
Red Light Cafe

GET READY TO SHIMMY!

We've lined up some
dynamic instructors at a
fabulous new venue – with vending, workshop and a spacious 300+ seat theater
in the same building!

3 Sensational Instructors
for Weekend Workshops!

 

Saturday, September 12

A Sparkling Showcase Event!

Bellydance Show
TBA

Sunday, September 13

Shimmy-a-thon's Hallmark!

Shimmy Contest & Entertainment
Crowning of the
2009 “Miss Shimmy”
TBA

Join us for the 5th Annual Shimmy-a-thon!

Saturday & Sunday  •  September 12 & 13

Hosted By:
SPSU



1100 South Marietta Pkwy.
Marietta, GA 30060

This unique event pairs the art & joy of bellydance with fundraising to help find a cure for Cystic Fibrosis (CF). CF is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the U.S. (70,000 worldwide).

All proceeds from the event will be donated to the
Cystic Fibrosis Foundation as part of their
GREAT STRIDES Campaign.

Shimmy-a-thon has raised over $76,000.00 with the generous support of our participants and sponsors!

Shimmy-a-thon encourages dancers to spread awareness about CF to friends, family, coworkers and their community and seek sponsors to support their efforts. We have some great prizes to award, so start soliciting sponsors early!

Together we can make a difference!

Medical Note: Because of risks to people with cystic fibrosis (CF), individuals with a confirmed positive sputum culture for Burkholderia cepacia complex shall not attend this event. This is because B. cepacia can be passed between individuals who have CF through close proximity. B. cepacia infection in a person with CF can cause serious respiratory illness and, in some patients, may lead to death. Despite this policy, there might still be some individuals with B. cepacia in attendance. B. cepacia is not a risk for otherwise healthy individuals. For alternative ways to participate and for information about this policy, please contact the CF Foundation at (800) FIGHT-CF or visit our web site at www.cff.org. Consult your CF care center physician with medical questions.