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10 people are interested
Taste of Utah 2016
ORGANIZATION: Cystic Fibrosis Foundation
This opportunity is provided by VolunteerMatch's partner.
Please visit the new page to apply.
Please visit the new page to apply.
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10 people are interested
On Saturday, November 12,2016 the Utah Chapter of the Cystic Fibrosis Foundation will be hosting the 18th annual Taste of Utah gala and auction at the Grand America Hotel. Taste is one of the premier social events in the state, featuring 25 of Utah’s exceptional dining establishments under the same roof for one night only. This event continues to be a highly anticipated local event, having raised over $2.2 million to fund research and improve the lives of people living with cystic fibrosis (CF), while also creating awareness and building local partnerships.
There are many opportunities to help make this year "taste" even more fantastic--participate in our "book club" by picking up a binder of vendors and hitting the phones and the pavement in your area; come hang out at the Salt Lake office for an afternoon of brainstorming ideas to round out auction packages; or simply recruit friends, family, and coworkers to the CF cause. We are also looking for night-of volunteers to assist in the setup and running of the Taste auction.
We will accommodate and cater to all of your scheduling needs, so if you’re interested in taking part and donating your time to Add Tomorrows, please feel free to drop Amanda Livnat a line at 801-532-2335 or alivnat@cff.org.
Let’s all help to make CF stand for "cure found!"
More opportunities with Cystic Fibrosis Foundation
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About Cystic Fibrosis Foundation
Location:
455 S 500 E, Suite 308, Salt Lake City, UT 84111, US
Mission Statement
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.
Description
Cystic Fibrosis is a life-threatening rare, genetic disease that affects the lungs, digestive system, and other major organs. Virtually every approved CF drug therapy available today was made possible because of the Foundation's support. In the 1950s, children born with CF seldom lived to attend kindergarten. Today, thanks to wise investments by the Foundation in CF research and care, the median predicted age of survival is now in the 30s and 40s. The Cystic Fibrosis Foundation is making great strides towards finding a cure for this disease and improving the quality of life for those born with CF.
CAUSE AREAS
Health & Medicine
WHEN
We'll work with your schedule.
WHERE
124 S 400 E Suite 250Salt Lake City, UT 84111
(40.766438 ,-111.880104 )
DATE POSTED
July 22, 2016
SKILLS
GOOD FOR
- Kids
- Teens
- People 55+
REQUIREMENTS
N/A