Disability

People with ALS Can Get Social Security Disability Benefits Sooner

June 17, 2021 • By

Last Updated: June 17, 2021

People with ALS Can Get Social Security Disability Benefits SoonerMay was Amyotrophic Lateral Sclerosis (ALS) Awareness Month. ALS is a progressive disease with no known cure. It advances rapidly and attacks the nerve cells responsible for controlling voluntary muscles. On average, 1,000 people with ALS apply for Social Security Disability Insurance (SSDI) benefits every year.

The ALS Disability Insurance Access Act of 2019 eliminates the required five-month SSDI waiting period for ALS applicants approved for benefits on or after July 23, 2020. The new law, however, does not affect our disability application or determination process.

This past month, we made the ALS claims processing even faster. Our system now automatically eliminates the five-month waiting period for ALS disability insurance claims. Previously, we had to prepare manual awards and send them to our Processing Centers for action—which took much more time. Now, we can help people with this debilitating disease in just a matter of days.

To give a real life example, a claimant with ALS recently submitted to us an online disability application. Using an electronic health exchange, we were able to collect sufficient medical evidence for the claimant and processed the claim in just two days. To learn more about how this process works, please visit our Disability Benefits Approval page.

Do you need to file for disability benefits? If so, we encourage you to apply online. You can check the status of your disability application online with your personal my Social Security account. Please share this information with your family and friends—and post it on social media.


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Mike Korbey, Deputy Commissioner for Communications

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  1. Santino J.

    My husband had ALS, first symptom was weakness in his fingers, one day, we had a dream life with early retirement and then, when we went to find out about the weakness, our whole world almost changed. There are so many things that can be said abt the suffering and frustration of people with ALS, we look back now and realize in many ways how lucky we were to found Multivitamin herbal cure that was able to get rid of my husband ALS disease totally, we had time to enjoy life and above all we all had time to also share this great testimony , many people lose loved ones without closure. I can’t imagine going thru all that you or your family had to live with daily, do not hesitate to contact w w w multivitamincare .org for ALS cure

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  2. Jane R.

    Amyotrophic Lateral Sclerosis is a serious illness that is rare (1,000 reported cases per year in the US), but it is a truly dire illness that can affect anyone.
    Government support is essential. The most important thing is not to treat those who have this disease somehow badly. People should continue to be a part of society and should not be outcasts. You need to lead an active social life (even on social networks like video chat) and enjoy life. I really hope that this incurable disease will soon be curable.

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