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The ALS Association Louisiana/Mississippi Chapter

 

Latest News


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May is ALS Awareness Month

Get involved and take a stand against Lou Gehrig's Disease. Get Started >>


Volunteer Opportunities

We are always looking for volunteers to serve on our committees or to serve in our office. If you are interested in current volunteer opportunities Click Here for details.

 


Double Your Donation!

Many companies offer matching gift programs to encourage employees to contribute to charitable organizations. Most programs match employee contributions dollar for dollar!

To find out if your company will match a contribution, please visit www.matchinggifts.com/als

 


Living with ALS  

Helpful and Informative Resources from our Care Service Coordinators

List of Care Services 
Handicap Accessbile Van Resources

Durable Medical Equipment Loan Closet

 Clinical Trials

 

 


Upcoming Events

  
ALS Awareness Night at Zephyr Field
Friday, May 11th
Game starts at 7PM


Roadmap to a Cure

Live Coverage

We are excited to announce that this year, for the first time ever, we'll be offering live video coverage of several important conference sessions to those at home, unable to make it to DC:

Monday, May 14:

9:15 -- 10:45 am EDT: Government ALS Research
11:00 am -- 12:30 pm EDT: Government ALS Research (repeat, not live)
2:00 -- 2:45 pm EDT: Advancing the Search for a Treatment: The MODDERN Cures Solution and PDUFA
4:00 -- 5:30 pm EDT: ALS Clinical Trials

These sessions will be available to watch live on ALS Association's Facebook page and at http://www.livestream.com/alsadvocacyday 


Louisiana State Advocacy Day
Wednesday, May 23, 2012
State Capitol 
12PM-4PM
Senate side of Rotunda


  BISTRO FOR THE ALS ASSOCIATION! 
May 21st from 5PM-9PM
Bistro Byronz
5412 Government St., Baton Rouge

20% of food sales from dine in orders & 10% of food on to go orders will support
ALS research.
Please tell server you are there supporting The ALS Association!

 

 

 

 

 

 

 

 

 

 

 

 

 
 
 
 
 
 
 
 
 

 


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OUR MISSION: Leading the fight to treat and cure ALS through global research and nationwide advocacy while also empowering people with Lou Gehrig's Disease and their families to live fuller lives by providing them with compassionate care and support.


The ALS Association Louisiana-Mississippi Chapter
(225) 343-9880 or (800) 891-3746 - P.O. Box 66825 - Baton Rouge, LA 70896-6825
All content and works posted on this website are owned and copyrighted by The ALS Association. ©2011