The ALS Association
yesterday at 14:47. Facebook
As Congress and President Trump begin a new term, we want to express our congratulations and a desire to work together to meet the needs of those living with #ALS.
The ALS Association
01/19/2017 at 13:42. Facebook
The ALS Association joined other organizations representing millions of Americans living with chronic, serious and life-threatening diseases, in a letter to President-elect Trump, to advocate for the needs of patients as the health insurance and health care systems are reevaluated. Read the letter here: [ Bit.ly Link ]

Letter to President Elect Trump

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The ALS Association
01/18/2017 at 19:20. Facebook
Cast your @INFINITIUSA Coaches' Charity Challenge vote for @SanDiegoState Coach Steve Fisher: [ Es.pn Link ]

Details | Infiniti Coaches' Charity Challenge

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The ALS Association
01/17/2017 at 21:49. Facebook
Thanks for tuning in to today’s ALS Virtual Listening Tour. We hope it was as helpful and informative for you as it was for us! Click here to listen to the recorded webinar: [ Bit.ly Link ]
The ALS Association
01/17/2017 at 18:02. Facebook
Want to learn more about ALS research? Tune into our webinar TODAY at 4 pm Eastern to hear from chief scientist Lucie Brujin, Ph.D. MBA as she discusses progress made and hope for the future: bit.ly/2ja0x1f
The ALS Association
01/17/2017 at 15:30. Facebook
Former Tennessee Titans linebacker Tim Shaw’s unexpected diagnosis of ALS doesn’t stop him from finding hope and advocating on behalf of those faced with #ALS. He has been an incredible ally of our ALS Association, Tennessee Chapter in fighting this disease. Below, we’ve included a Q/A with Tim, which includes information about his new book, “Blitz Your Life.” The story, according to its...
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Blitz Your Life

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The ALS Association
01/16/2017 at 19:40. Facebook
If you haven’t heard, our ALS Virtual Listening Tour is just two days away on Jan 18 at 1 pm! Sign up now and hear from people living with ALS and their caregivers as they share their thoughts and ideas directly with ALS Association President and CEO, Barbara Newhouse. [ Bit.ly Link ]

The ALS Association WebEx Enterprise Site

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The ALS Association
01/15/2017 at 23:37. Facebook
We are proud to be on the front lines of research sponsoring clinical trials, supporting innovative projects and developing new therapies to treat ALS: [ Bit.ly Link ]

Stem Cells

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The ALS Association
01/14/2017 at 17:14. Facebook
From leading on innovative ideas to advancing treatments for people living with #ALS, our scientists continue to uncover significant discoveries. Read about our latest research: [ Bit.ly Link ]

Research Home Page

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Looking back at 2016’s memorable moments makes us so excited for what 2017 has to offer! #FBF [ Bit.ly Link ]

This Year’s 10 Biggest Advances in ALS Research

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Thanks to our donors’ generosities, we are able to work with large global initiatives like the New York Genome Center and Project MinE to research genes related to ALS and develop therapies to treat the disease: [ Bit.ly Link ]

Genetics

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If you haven’t done so already, please take a moment to register for the next Virtual ALS Listening Tour to be held on Wed., Jan. 18 at 1 pm. This is an important event where people living with #ALS and their caregivers have an opportunity to share their thoughts and ideas directly with ALS Association President and CEO, Barbara Newhouse. [ Bit.ly Link ]

The ALS Association Virtual Listening Tour

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Tune in to our webinar on 1/17 at 4pm to learn more about our ALS Research Progress from our chief scientist Lucie Brujin, Ph.D. MBA. Register here: [ Bit.ly Link ]

The ALS Association WebEx Enterprise Site

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Check out our recap from last month’s Prize4Life: Accelerating Research for ALS/ Lou Gehrig's Disease and The ALS Association #ALS Assistive Technology Challenge finals in Dublin! [ Bit.ly Link ]

The Official Blog of The ALS Association on WordPress.com

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About a month ago, The ALS Association participated in the International Symposium on ALS/MND in Dublin! Top researchers gathered to share their findings and thoughts on fighting ALS. Throughout the symposium, we captured the best tweets to share in our blog: [ Bit.ly Link ]

Hopeful Highlights from the Recent ALS MND Symposium

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The ALS Association visited Capitol Hill this week with staff from @SenatorWhitehouse and @SenatorTomCotton to discuss legislation removing the five-month waiting period for Social Security Disability Insurance. We were pleased to hear the legislation will be introduced in February 2017, but we’ll still need your support! So please sign up today to become an advocate for this important piece...
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Registration

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Have you registered for the next Virtual ALS Listening Tour? This online event being held on Wed., Jan. 18 at 1 p.m., and will give people living with #ALS and their caregivers an opportunity to share their thoughts and ideas directly with ALS Association CEO Barbara Newhouse and members of the National Board of Trustees. Register today! [ Bit.ly Link ]

The ALS Association WebEx Enterprise Site

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Our website features the latest research news & information as we work to improve the lives of people living with ALS. Find our research webinars, newsletters, blog posts, and more, here: [ Bit.ly Link ]

Research News

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More than 5,000 people are diagnosed with #ALS every year. Watch this video to learn more: [ Bit.ly Link ]
Supporting the fight against ALS means the world to San Diego State University's Coach Steve Fisher whose son is battling the disease. Vote for him in the INFINITI Coaches' Charity Challenge at [ Es.pn Link ] #Fisher4ALS

Details | Infiniti Coaches' Charity Challenge

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