ALS is a devastating disease - physically, emotionally, financially, and logistically. Our goal is to alleviate as much of a family's burden as we can. The ALS Assocociation Louisiana-Mississippi Chapter helps people with ALS and their families cope with the day to day challenges of living with ALS by providing information, resources, and referrals to make sources. 

Simply put, we could not do the work that we do to support individuals with ALS, families, and caregivers without your partnership.

2019

THE NEED FOR SUPPORT: $250,000

Care Services  |  Clinics  |  Caregiver Support  |  Research & Advocacy 

Your support will enable us to act urgently with our targeted plan to improve the quality of life for people with ALS and their families. To that end, we will fund new and innovative technologically supported solutions that will allow families to remain physically and emotionally healthy, together, safely in their own homes, and to help them to live a life beyond ALS. 

We are committed to continuing our support of ALS caregivers through expansions of our in-home caregiver relief program, and we will continue to fight for and fund global research efforts to eradicate ALS entirely.