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3rd Annual Link Up for the Cure Austin

3rd Annual Link Up for the Cure Austin

Saturday, June 21, 2008 at 8:00 AM (CT)

Manor, TX

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Ticket Information
Ticket Type Sales End Price Fee Quantity
Individual Player   more info Ended $110.00 $0.00 N/A
Twosome   more info Ended $110.00 $0.00 N/A
Foursome   more info Ended $110.00 $0.00 N/A
Silver Sponsor:   more info Ended $150.00 $0.00 N/A
Gold Sponsor:   more info Ended $550.00 $0.00 N/A
Platinum Sponsor:   more info Ended $1,500.00 $0.00 N/A
DONATE A GIFT FOR THE AUCTION:   more info Ended $0.00 $0.00 N/A
CAN'T ATTEND? DONATE NOW!   more info Ended N/A
Event Details
Link Up for Our Boys!  Link Up for Life!

Duchenne muscular dystrophy is the most common form of muscular dystrophy.  This disorder affects one in every 3,500 boys and is the leading genetic killer of young boys worldwide.

Please join us in our quest to uncover a cure for Duchenne muscular dystrophy by participating in the 3rd Annual Link Up for the Cure Golf Tournament at ShadowGlen Golf Club in Manor, TX.

  • DATE:             Saturday, June 21, 2008
  • TIME:              8:00AM - Shotgun Strt
  • FORMAT:        Four Person Scramble
  • FEE:                Donation of $110/Player
                           (includes Green Fees, Cart & Awards Lunc)
  • AWARDS:       1st Place:    Oakley Watches
                           2nd Place:   Oakley Sunglasses
  • PRIZES:          Longest Drive, Closest to Hole, Accuracy Challange
  • AGENDA:        7:00am - 7:45am   -  Registration & Snack
                               7:45am - 7:55am   -  Players to Carts
                               8:00am                 -  Tee Off 
                               1:00pm                 -  Awards Luncheon

Proceeds from this event will fund research for the cure and trreatment of Duchenne muscular dystrophy.

Federal 501(c)(3) Tax ID #:  20-0299958

www.cureduchenne.org 

 

When

Saturday, June 21, 2008 at 8:00 AM (CT)

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Where
ShadowGlen Golf Club
12801 Lexington Street
Manor, TX 78653



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Hosted By

CureDuchenne

CureDuchenne is fighting for the lives of the 1 in every 3500 boys who are stricken with Duchenne Muscular Dystrophy. Most of these boys will not live past their teens. Their muscle cells will die and won't regenerate. It can happen in any family. But finally, thanks to recent scientific breakthroughs, THERE IS HOPE!

CureDuchenne is a not-for-profit organization founded by Corona del Mar (California) parents of a Duchenne boy. Unlike other organizations that simply fund research, CureDuchenne demands more. They are fighting to bring the most promising research out of the labs and into clinical trials that can save THIS generation of Duchenne boys. YOU can help us bring lifesaving treatments to market and give them a chance for a life.

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