Tuesday, June 12, 2012

CF Fundraiser Cut-A-Thon at Glow Spa Salon, Oakland CA July 1, 2012


387 Grand Ave, Oakland, CA 94610
Cut-A-Thon
Sunday, July 1st 10am-2pm
Haircuts $25! Add on a Blow Out for $20!
100% of proceeds go towards life saving research for the
Cystic Fibrosis Foundation / www.cff.org
What Is Cystic Fibrosis?
Cystic fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the United States (70,000 worldwide). A defective gene and its protein product cause the body to produce unusually thick, sticky mucus that:
         • clogs the lungs and leads to life-threatening lung infections; and
         • obstructs the pancreas and stops natural enzymes from helping                   the body break down and absorb food.
In the 1950s, few children with cystic fibrosis lived to attend elementary school. Today, advances in research and medical treatments have further enhanced and extended life for children and adults with CF.
Event Details: Appointments can be made in person or by calling
(510) 452-GLOW, with pre-payment of cash, check, debit or credit.  Please make checks payable to Glow Spa & Salon. Walk-ins welcome!
Mail or drop off in-kind donations to:
Glow Spa & Salon 387 Grand Ave, Oakland, CA 94610. (510) 452-GLOW
A receipt for your donation will be provided.
Nail, massage, and skin care services are available the day of the event. 
Please book online www.glowspasalon.net
| Adding tomorrows every day.
Because of risks to people with cystic fibrosis (CF), individuals who have had a confirmed positive sputum culture for Burkholderia cepacia (B. 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 www.cff.org. Consult your CF care center physician with medical questions.

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