ALS Association Louisiana CIO

PO Box 1730
Covington, LA  70435
Phone: (225) 343-9880

We are a service provider, a resource and advocate for people afflicted by ALS also known as Lou Gehrig Disease.

The ALSA Louisiana Chapter was founded in April, 2005 to serve the needs of those living with Amyotrophic Lateral Sclerosis and their caregivers.

The ALS Association is the only national not-for-profit health organization dedicated solely to the fight against ALS. The Louisiana Chapter 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 Louisiana Chapter is a 501(c)3 organization.

The ALS Association (National Office and the Louisiana 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 Louisiana 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.