The Als Association


The Als Association is listed in the Non Profit Organizations category in Agoura Hills, California. Displayed below are the social networks for The Als Association which include a Facebook page, a Linkedin company page, a Twitter account and a YouTube channel. The activity and popularity of The Als Association on these social networks gives it a ZapScore of 98.

Contact information for The Als Association is:
27001 Agoura Rd
Agoura Hills, CA 91301
(818) 340-0182
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The Als Association Contact Information:

Social Posts for The Als Association

Thanks to the #icebucketchallenge and @TShawsTruth, @Calaneet Balas sees promising breakthroughs ahead:

Tim Shaw is an inspiration to the ALS community. While battling ALS, he and the Tennessee Titans raised awareness with the Ice Bucket Challenge and helped fund research for people living with ALS.
Three years after being diagnosed with ALS, Shaw’s goals are simple — but even more meaningful, he says.

.@TShawsTruth is an inspiration to the ALS community. His work raising awareness while battling #ALS is amazing:

The ALS Association needs your help passing the #ALS Disability Insurance Act (S.379/ H.R. 1171)! The bills eliminate the 5 month waiting period for Social Security Disability Insurance and Medicare. Check to see if your Senators and Representatives have already co-sponsored the Senate and House versions. If they have not, please ask them to do so. Ask your Senator to co-sponsor S. 379. Ask your Representative to co-sponsor H.R. 1171. If they are already on the bills, thank them. Contact your Senators and Representatives here:
Find contact information for federal, state, and local government officials.

Find your senator's number and call your rep. to support the #ALS Disability Insurance Act, SB379:…

More info on the #ALS Disability Insurance Act! Learn more about how this bill benefits people living with ALS:…

If the #ALS Disability Insurance Access Act passes, this would waive the Social Security Disability Insurance five-month waiting period. However, we need your support to make it happen! Learn more about this legislation and stay tuned for details on how you can help advocate on behalf of people living with ALS:
Learn how you can help The ALS Association advance scientific research to find a cure for ALS, provide resources for people with ALS and their loved ones, heighten awareness of the nature of the disease, and encourage government leaders to expand their support of research and patient care.

Dr. Ozlinder @NUFeinbergMed further solidifies upper motor neuron contribution to #ALS. Find out how!

Dr. Ozlinder’s team Northwestern University Feinberg School of Medicine further solidifies upper motor neuron contribution to #ALS. The ALS Association is proud to support their studies! Find out more!
ALS is characterized by the progressive loss of motor neurons – both upper motor neurons (UMNs) and lower motor neurons (LMNs). Within the ALS scientific community there has been a debate how UMNs …

We held another ALS Listening Tour in January to hear questions and comments from the #ALS community. You can check out some of the questions and answers in our latest blog post:
In January, CEO and President Barb Newhouse hosted a Listening Tour with Association staff leaders, BOT Chairman Doug Butcher and Bill Thoet, former BOT Chairman and current Chairman of The Associa…