Mark your calendars! Our next Mingus Awareness Project concert is coming soon --
Sunday, December 7 (7 p.m.)
5311 South Lake Park Ave West
$20 / $15 for students
On December 7, a group of musicians will gather at The Promontory to celebrate the life and music of Charles Mingus, and to benefit the Les Turner ALS Foundation. Mingus, an American musical hero who died of ALS, is one of the greatest figures in jazz history. His bass playing, compositions and philosophy have transcended his genre and left indelible marks on music history.
The MAPtet performs two sets of music:
Rebecca Cohn -- trombone
Paul Hartsaw -- tenor saxophone
Jon Hey -- piano
Juli Wood -- baritone saxophone
Dan Godston -- trumpet
Michael Hesiak -- alto saxophone
Jon Godston -- soprano saxophone
Tom Berg -- clarinet, flute and bass clarinet
Alex Wing -- upright bass
Damon Short -- drums
with special guest Renée Baker (violin)
This Mingus Awareness Project concert is presented by the Borderbend Arts Collective, in partnership with the Les Turner ALS Foundation. More than a dozen Mingus Awareness Project concerts have happened since its inception in 2007. Mingus Awareness Project concerts have happened in the Chicago area (at the Velvet Lounge, Jazz Showcase, Hideout, HotHouse, Martyrs’ and Fitzgerald’s) and Richmond, Virginia (at the Camel, Rhythm Hall, and Balliceaux).
Attendees will have opportunities to participate in a raffle during the event. Donations can be made to the Les Turner ALS Foundation via the Mingus Awareness Project link. Your donations are greatly appreciated. All proceeds will go to benefit the Les Turner ALS Foundation.
Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig’s disease or motor neuron disease (MND), causes motor neurons to stop working and die. The result is loss of voluntary movement and muscle functions such as speaking, swallowing, and breathing. ALS occurs regardless of race, ethnicity or socioeconomic status. ALS is most common between 40 and 70 years of age, although it can strike at any age. In the US, someone is diagnosed every 90 minutes, and 35,000 people are living with ALS. Average lifespan is three to five years from diagnosis. Approximately 10% of all cases are inherited forms, and a faulty protein pathway is known to play a role in all types of ALS. Though treatment of symptoms often improves quality of life, there is no cure for ALS.
poster images by Josh Josue
About the Les Turner ALS Foundation
Since 1977, the Les Turner ALS Foundation has been a leader in research, patient care, and education about Amyotrophic Lateral Sclerosis (ALS), better known as Lou Gehrig's disease, and other motor neuron diseases (MND). The Foundation serves more than 90% of the ALS population in the Chicago area. The Foundation is also one of the nation's largest independent ALS organizations and has raised nearly $45 million to fight Lou Gehrig's disease. In addition, through wide-ranging research and symposiums for healthcare professionals, the Foundation reaches the ALS community worldwide. The Foundation is affiliated with Northwestern Medicine and is a founding member of the International Alliance of ALS/MND Associations.