The Als Association

98
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

"The Als Association" - ZapScore Report

98
The Als Association has an overall ZapScore of 98. This means that The Als Association has a higher ZapScore than 98% of all businesses on Zappenin. For reference, the median ZapScore for a business in Agoura Hills, California is 36 and in the Non Profit Organizations category is 37. Learn more about ZapScore

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Social Posts for The Als Association


We support more than 150 labs around the globe. Learn about the #ALS scientists & projects we fund:†twitter.com/i/web/status/8…

On Monday, May 22, at 2 pm, catch the latest Care Service Webinar hosted by our Senior Director of Clinical Programs, Nicole Yarab. She will discuss the benefits of early intervention and the multidisciplinary approach to ALS care. http://bit.ly/2pPPaT0

We proudly salute our troops on National Armed Forces Day. Did you know that veterans are twice as likely as the rest of the population to be diagnosed with ALS? Learn more at http://bit.ly/2nvx32j
ALS, or amyotrophic lateral sclerosis, is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord.


DYK: Veterans are twice as likely as the rest of the pop to be diagnosed w/ #ALS? Learn more†twitter.com/i/web/status/8…


Hear from the Phelan family, just 1 of many stories told this week at the #ALS Advocacy Conference #ALSHillDay17:†twitter.com/i/web/status/8…

Hear from the Phelan family, just 1 of about 600 stories told this week at the #ALS Advocacy Conference #ALSHillDay17 http://bit.ly/2rAnBdx
Thank you to the over 600 people that descended on Capitol Hill on Tuesday during The ALS Association’s 2017 Advocacy Conference. So many advocates shared their stories to inspire their local…

This week, over 600 people descended Capitol Hill for ALS Association’s 2017 Advocacy Conference! We would like to specially thank the many advocates who shared their stories to inspire their local legislators to support important ALS initiatives. Here’s a quick recap of how one inspiring family empowered Congresswoman Bonnie Watson Coleman. http://fal.cn/u1Hv #ALSAware #ALSAwarenessMonth
Thank you to the over 600 people that descended on Capitol Hill on Tuesday during The ALS Association’s 2017 Advocacy Conference. So many advocates shared their stories to inspire their local…


RT @cathymcmorris: The Steve Gleason Enduring Voices Act ensures that Medicare and Medicaid cover speech-generating tech for those with deg…


RT @CDCEnvironment: Share your information with the National #ALSRegistry so we can learn more about possible causes. https://t.co/2gFptApc…

Tune in on Monday, May 22 at 4 pm to the next webinar in our ALS Clinical Trial Pipeline Series. Dr. Merit Cudkowicz, from Massachusetts General Hospital will deliver the latest news on ALS clinical trials and answer questions about the current state of clinical research. http://bit.ly/2qWjJqd