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Bettin' on a Cure for ALS

The Allen Family and The ALS Association Texas Chapter

Saturday, November 17, 2012 from 7:00 PM to 11:00 PM (CST)

Dallas, TX

Bettin' on a Cure for ALS

Ticket Information

Ticket Type Sales End Price Fee Quantity
Individual Ticket   more info Ended $35.00 $0.00
Date Night Special   more info Ended $30.00 $0.00

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Event Details

Join us at The House of Blues Dallas for Bettin’ on a Cure, from 7p - 11p on Saturday, November 17th, 2012 with Casino running from 7:15pm - 10:15p and then the distribution of prizes immediately following. Each attendee will receive food, non-alcoholic beverages, limited alcoholic beverages (more are always available for purchase), $500 in casino chips to start the betting off, access to live music, DJ and other fun live entertainment.

All proceeds from Ticket and Casino Sales will go directly to The ALS Association Texas Chapter to help in your local communities.

 

The ALS Association is the only national not-for-profit health organization dedicated solely to the fight against ALS. ALSA covers all the bases — research, patient and community services, public education, and advocacy — in providing help and hope to those facing the disease. The ALS Association (National Office and the Texas Chapter) operates under a shared mission: to help people living with Amyotrophic Lateral Sclerosis and to leave no stone unturned in search for the cure.

 

For Corporate, Individual Sponsorships and In-Kind Donations please contact BettinOnACureForALS@gmail.com

Have questions about Bettin' on a Cure for ALS? Contact The Allen Family and The ALS Association Texas Chapter
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When & Where


House of Blues - Dallas
2200 North Lamar
Dallas, TX 75202

Saturday, November 17, 2012 from 7:00 PM to 11:00 PM (CST)


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Organizer

The Allen Family and The ALS Association Texas Chapter

 

My name is Holly Potter-Harvey and Linda and Marshall Allen are my Aunt and Uncle. This is something that my family and I hold close to our hearts. On October 27, 2000 my uncle Marshall Allen lost his battle with ALS, and this year his wife Linda Allen was also diagnosed with ALS making them 1 out of approximately 10 couples in the WORLD who have both been diagnosed with this heinous disease.  My family helped build this association and my Uncle lobbied for research to help find a cause and a cure. Now we need your help!

 

 

The ALS Association is the only national not-for-profit health organization dedicated solely to the fight against ALS. ALSA covers all the bases — research, patient and community services, public education, and advocacy — in providing help and hope to those facing the disease. The ALS Association (National Office and the Texas Chapter) operates under a shared mission: to help people living with Amyotrophic Lateral Sclerosis and to leave no stone unturned in search for the cure.

We work together to accomplish our mission. The Texas Chapter focuses primarily on helping local patients and families live with ALS while the National Office focuses primarily on research and advocacy. The Chapter supports the National Office through revenue sharing and research contributions. The National Office supports the Chapters by providing up-to-date information and materials.

Our accomplishments are made possible by the generosity of others. From the smallest donation to the largest gift, donors touch the ALS community with hope for the future.

  Contact the Organizer

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