New Report Highlights Heightened Risk of ALS in Military

New Report Highlights Heightened Risk of ALS in Military

Washington, D.C. (May 03, 2019) — People who have served in the military are at a greater risk of developing ALS and dying from the disease than those with no history of military service, according to research released by The ALS Association.

May is ALS Awareness Month

The 2019 ALS in the Military report compiles findings from research conducted going back to the early 1990s when it was observed that ALS was occurring in Gulf War veterans at unexpected rates.

The data shows that ALS is connected to military service regardless of the branch of service or whether serving during peacetime or in war.

In 2008 the Department of Veterans Affairs established ALS as a service connected disease. Since then the average number of veterans living with ALS increased by 30 percent.

जब चली गई खुद की आवाज तो बना डाला टेक्स्ट टू स्पीच ऐप

“Study after study has shown that our military heroes are more likely to develop ALS, which is why it is critical that Congress fully funds the ALS Research Program at the Department of Defense, as well as research at the National Institutes of Health,” said Calaneet Balas, president and CEO of The ALS Association.

पेशीशोषी पार्श्व काठिन्य (Amyotrophic lateral sclerosis) ALS  क्या है?

“Research into the causes of and treatments for ALS can benefit veterans and nonveterans alike,” she added.

About ALS

ALS is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord. Over the course of the disease, people lose the ability to move, to speak, and eventually, to breathe. On average, it takes about a year before a final ALS diagnosis is made. The disease is always fatal, usually within five years of diagnosis. There is no cure.

भयंकर बीमारी एएलएस के बारे में फास्ट फैक्ट्स

About The ALS Association

The ALS Association is private funder of ALS research in the world. The Association funds global research collaborations, provides assistance for people with ALS and their families through their nationwide network of chapters and certified clinical care centers, and advocates for better public policies for people with ALS.

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