People with ALS are at an increased risk for respiratory problems associated with viral infections.
People with ALS are at an increased risk for respiratory problems associated with viral infections.
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COVID-19 UPDATE
What is Respite?
Being a family caregiver, while a fulfilling role, can consume a great deal of physical, mental, and emotional energy. Respite simply means an interval of rest or relief. The ALS Association will reimburse a partner agency in your area to step in as caregiver for up to 18 hours each month so that you can take a break.
Connecting ALS
Have you heard about our new podcast addressing the disease from virtually all angles? New episodes of Connecting ALS are released each month. Subscribe today!
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Volunteer
Our programs and services for people living with ALS and their families would not be possible without volunteers. Whether you are looking to volunteer one day a year at a special event or weekly for a family affected by ALS, we have something for you.
Get Involved
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- A Deeper Look into ALS Association Efforts to Speed Approval of Gene Therapies
March 4, 2020 - Preemptive Actions to Help Prevent the Spread of Respiratory Diseases
March 3, 2020 - How the Walk to Defeat ALS Has Grown Over 20 Years
February 24, 2020 - The ALS Association and Project ALS to Fund Columbia University Drug Trial for Patients with Rare Genetic Forms of ALS
February 14, 2020
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