At Modern Luxury, connection and community define who we are. We use cookies to improve the Modern Luxury experience - to personalize content and ads, to provide social media features and to analyze our traffic. We also may share information about your use of our site with our social media, advertising and analytics partners. We take your privacy seriously and want you to be aware that we have recently made changes to our Privacy Policy, which can be found here.


Muscular Dystrophy Association's 14th Annual Taste of the Town

| August 19, 2014 | Calendar

The Muscular Dystrophy Association’s (MDA) 14th Annual Taste of the Town is returning to Scottsdale Quarter Friday, October 17 at 6:30 p.m. for a night of fine cuisine, spirits, live music and a first-class silent auction. The event, presented by Cigna, will feature more than 25 vendors showcasing their fine wine and gourmet dishes and live entertainment by Elvis Before Noon. As one of the most distinguished charity events in the Valley, Taste of the Town benefits more than 2,400 Arizona families affected by neuromuscular diseases.

For $75, guests can dress to impress for an evening of dancing, drinks and delicious food, all while helping the MDA assist Arizona families who are battling this disease. After Friday, Oct. 3, admission increases to $100.

Founded in 1950, the Muscular Dystrophy Association, a voluntary national health agency consisting of a combination of both scientists and citizens, strives to combat a variety of neuromuscular diseases that affect more than 1 million Americans. MDA is the nation’s largest nongovernmental funder of scientific research seeking better treatments and cures for the more than 40 neuromuscular diseases in its program. Through research, support services and community education, the MDA is helping fight muscle disease.

About MDA
The Muscular Dystrophy Association (MDA) is the world’s leading nonprofit health agency dedicated
to finding treatments and cures for muscular dystrophy, amyotrophic lateral sclerosis (ALS) and other
neuromuscular diseases. It does so by funding worldwide research; by providing comprehensive health
care services and support to MDA families nationwide; and, by rallying communities to fight back
through advocacy, fundraising and local engagement. Visit and follow us at and @MDAnews.


Photography by: