Saline's Winter Beach Blast
"Party for Breath" 2010

Thank You for Making This Event So Great!

We Raise Over 25,000 Again! We will give you the update soon.

Go to 56 Daze Website to see some great photos of the night.

We have raised over $150,000 total for CF!

Is the Winter Beach Blast just another ’Charity Fundraiser’? Not exactly!! This event features an affordable price tag, fantastic entertainment, finger food, great silent auction items to bid on, and plenty of attractive drawing items.

Emily Schaller-Guest Speaker

Emily Schaller, 27, is a heroine with one goal in mind. Rock CF! Take one look at this native Detroiter and it’s plain to see. Emily Schaller does not take guff. Equal parts spark and wit, Emily is claiming her victories against cystic fibrosis having launched Rock CF Foundation in summer of 2007. Today Emily’s battle against this deadly genetic disease is printed in magazines and posted on websites, her greatest victories being raising $150,000 for cystic fibrosis research and securing a sponsorship of $20,000 from New York-based Spin magazine for Rock CF Foundation’s annual benefit concert. More>>

Top Notch Entertainment

This year we will have comedian Kevin McPeek and 56Daze as our headline band. More>>

Mark your calendar and buy your tickets to this exciting event for such a good cause.

OUR MISSION: To promote awareness and educate people about CF and to raise money to fund research so that we can expand the lives of those with CF.

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Because of risks to people with cystic fibrosis (CF), individuals with 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 on the CF Foundation call (800) FIGHT-CF or visit our website about this policy at www.cff.org. Consult your CF care center physician with medical questions.

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