ALS Ice Bucket Challenge Progress
  • Sign up
  • |
  • Login
  • |
  • Find local services
  • |
  • |

For several weeks we have witnessed the devastating effects of the coronavirus pandemic. Covid 19 has upended the world and life as we know, as we are told to- self isolate, shelter in, practice safe hygiene to mitigate the affects of this monster with no cure. Unfortunately, this is the everyday reality of persons living with Amyotrophic Lateral Sclerosis (ALS) , a progressive neurodegerative disease, a silent killer with no known cure. ALS destroys lives, enhances fear and anxiety, and the financial burden of treating this disease destroys entire families economically. Respirators,  ventilators and multidisciplinary medical care allow ALS patients to sustain life daily.


So as we stand in complete support of  those affected by COVID 19- medical professionals, first responders, grocery store employees, sanitation workers, impacted families, and above all those brave patients fighting for their lives.
Please remember and continue to support those who live this reality daily, Alabama’s ALS community. Every gift matters!


The safety of the ALS community is always our top priority. Out of an abundance of caution, the Alabama Chapter has postponed our Huntsville Wine and Dine Spring Soiree, Mobile and Birmingham Empowered Workshops, State Advocacy Day, and March and April community events and support groups. We are continuing to evaluate our planned Chapter’s Community Outreach events scheduled in May and beyond, in accordance with the Centers for Disease Control (CDC) and state Department of Public Health (DPH) guidelines. We are promoting everyday preventive health actions to all our participants and staff. We discourage anyone who is sick or who represents a vulnerable population, including persons with ALS, from attending community events in-person. Please visit our website frequently to stay current on our response to the evolving news about the coronavirus(COVID-19).

 

 

Prevent the Spread of Coronavirus
People with ALS are at an increased risk for respiratory problems associated with viral infections.

 

The safety of the ALS community is always our top priority. Out of an abundance of caution, the Alabama Chapter has postponed our March and April community events and support groups. We are continuing to evaluate our planned Chapter’s Community Outreach events scheduled in May and beyond, in accordance with the Centers for Disease Control (CDC) and state Department of Public Health (DPH) guidelines. We are promoting everyday preventive health actions to all our participants and staff. We discourage anyone who is sick or who represents a vulnerable population, including persons with ALS, from attending community events in-person. Please visit our website frequently to stay current on our response to the evolving news about the coronavirus(COVID-19).



 

 


 

Spirit of Lou Gehrig Honoree Video

 


 

Our Mission
To discover treatments and a cure for ALS, and to serve, advocate for, and empower people affected by ALS to live their lives to the fullest.

Thank You to Our Statewide Partners



Thank You to Our Statewide Partners




















Get Involved With Us
Help create a world without ALS by getting involved in the way that best suits YOU! When you fundraise with friends and family you take us closer to discovering a cure.

Walk to Defeat ALS

More than 180 walks take place in communities across the country February through November. Walk to Defeat ALS draws people of all ages and athletic abilities coming together to honor a loved one with the disease, to remember those who’ve passed and to show their support for the cause.

Find A Walk Near You

junior board get involved size

Join the ALS Association Junior Board

Do you know a young professional who wants to make a difference in your community, learn a new set of skills and share their talents, meet new people and share meaningful experiences and support the mission of the ALSA? Please visit here to learn more and fill out our interest form.

Discover More Ways to Help Fight ALS
Resources

Whether you’re newly diagnosed, navigating your journey with the disease, caring for a person with ALS, or researching the cure, there are resources to support you.

Let us help you and your family cope with the day-to-day challenges of living with ALS.

For People with ALS

Learn about our grant program, upcoming scientific meetings, and opportunities to collaborate.

For Researchers

Caring for someone with ALS is hard work. We offer resources and support to help you.

For Caregivers
Stay Connected With Us

Sign up to receive the latest news in ALS and learn how you can continue making a difference in the search to treat and cure this disease.

You Can Help Create A World Without ALS

Your gift will help The ALS Association support research to find a cure for ALS and provide much-needed services to patients and their families. By becoming a part of The ALS Association family and making your gift today, you will help sustain hope in thousands of people affected by ALS.