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The ALS Association
The ALS Association National Office / Fighting Lou Gehrig's Disease
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The ALS Association 9h
“Losing my ability to speak has forced me to be a better listener," Gene Connolly said. "Now I hear more than a person’s words." The short film, “Mr. Connolly Has ALS,” can be streamed online until 7/11. Learn more:
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The ALS Association 13h
Yankees fan or not, you've got to love this video of Co-founder Pat Quinn that was shown during the Yankees pre-game yesterday, in honor of Lou Gehrig's birthday. Pat never stops raising !
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The ALS Association 15h
(1/2) Congrats to the Senate on ; now 290 House co-sponsors are needed for H.R.5499: . Congress should also act on ALS Disability Insurance Access Act (S.379, H.R.1171) to end the 5-month waiting period for SSDI.
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The ALS Association 15h
(2/2) People with should get SSDI & care when they need it. Urge your members of Congress to act now on ALS Disability Insurance Access Act (S.379, H.R.1171).
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The ALS Association Jun 19
We look forward to an engaging, informative conversation between the ALS community & representatives from the & the pharmaceutical industry on 7/12. Learn more about how to participate virtually here:
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The ALS Association Jun 19
Donate today to support our capacity to fund , like Pison’s groundbreaking assistive technology: . will match all gifts up to a total of $25K!
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The ALS Association Jun 19
Pison Technology aims to develop products to improve the lives of people w/ . In 2016, Pison won $100,000 through our ALS Assistive Technology Challenge, started in partnership w/ Prize4Life. Here's an update:
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The ALS Association Jun 19
Take the first step. Register for the today!
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The ALS Association Jun 18
By raising , we can take a great step forward in the effort to find a cure. Find out how your voice can make a difference:
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The ALS Association Jun 17
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The ALS Association Jun 17
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The ALS Association Jun 16
(1/2) Congrats to the Senate on ; now 290 House co-sponsors are needed for H.R.5499: . Congress should also act on ALS Disability Insurance Access Act (S.379, H.R.1171) to end the 5-month waiting period for SSDI.
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The ALS Association Jun 16
(2/2) People with should get SSDI & care when they need it. Urge your members of Congress to act now on ALS Disability Insurance Access Act (S.379, H.R.1171).
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The ALS Association Jun 15
Traveling brings an array of challenges for families affected by . Our free 6/18 webinar will discuss safe, enjoyable travel options for people living with ALS & their families & caregivers. Register now:
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The ALS Association Jun 14
(1/2) Congrats to the Senate on ; now 290 House co-sponsors are needed for H.R.5499: . Congress should also act on ALS Disability Insurance Access Act (S.379, H.R.1171) to end the 5-month waiting period for SSDI.
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The ALS Association Jun 14
(2/2) People with should get SSDI & care when they need it. Urge your members of Congress to act now on ALS Disability Insurance Access Act (S.379, H.R.1171).
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The ALS Association Jun 14
REMINDER! RSVP for in-person attendance of the 7/12 Community Workshop: Developing Drugs for Treatment, Guidance for Industry in Washington, D.C., by TOMORROW, 6/15. Share your voice w/ the & industry!
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The ALS Association Jun 14
50% off registration! Calling all RUNNERS! Run through the beautiful Napa & Sonoma Valleys for an amazing cause! Join for the Napa-to-Sonoma Wine Country Half Marathon on 7/15! Contact kjohnson@alsagoldenwest.org for a special discount code!
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The ALS Association retweeted
Kim Wallis Jun 13
Excited to take part in Charity Bracket Challenge with ! Less excited to go up against in the 1st round but who doesn’t love an underdog?? More👉
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The ALS Association Jun 14
Nats fans, check it out! Thanks and !
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