The ALS Association @alsassociation Twitter profile

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The ALS Association

6 months

ALS, or amyotrophic lateral sclerosis, is a disease that robs people of the ability to walk, talk, and breathe. There is no cure for #ALS yet. Learn more:

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The ALS Association

@alsassociation

3 years

(1/4) We are deeply saddened to share that Pat Quinn, co-founder of the ALS Ice Bucket Challenge passed away at the age of 37. Pat was diagnosed with ALS in 2013 and went on to help popularize the greatest social media campaign in history.

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The ALS Association

@alsassociation

6 years

Carmen Schentrup was killed in the Parkland mass shooting. Because #CarmensDream was to become a medical researcher & discover a cure for #ALS , her parents have created the Carmen Schentrup ALS Research Fund. Join us in Carmen's quest to find a cure:

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The ALS Association

@alsassociation

6 years

"However difficult life may seem, there is always something you can do and succeed at. It matters that you don't just give up." -- Stephen Hawking

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The ALS Association

@alsassociation

3 years

(2/4) The Ice Bucket challenge dramatically accelerated the fight against ALS, leading to new research discoveries, expansion of care for people with ALS, and greater investment by the government in ALS research.

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The ALS Association

@alsassociation

3 years

(3/4) Pat continued to raise awareness and funds for the fight against ALS and our thoughts are with the Quinn family and all of his friends and supporters. Pat was loved by many of us within the ALS community and around the world.

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The ALS Association

@alsassociation

3 years

(4/4) He will be missed, but he will continue to inspire us until we have a world without ALS. Read more:

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The ALS Association

@alsassociation

8 years

The #IceBucketChallenge impact grows as researchers identify one of the most common gene contributors to #ALS

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The ALS Association

@alsassociation

6 years

@alsassociation BOT Chair Stephen Winthrop on Hawking: "Most people describe ALS as a disease that, bit by bit, robs a patient’s ability to move and function. But Stephen Hawking has inspired me to focus on what I can do, rather than what my body can no longer do."

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The ALS Association

@alsassociation

6 years

Today we remember Stephen Hawking, who inspired the ALS community and the world. Our thoughts are with his family.

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The ALS Association

@alsassociation

2 years

(1/2) BREAKING NEWS: @US_FDA approved AMX0035, a new treatment that has been shown to slow progression of #ALS and extend life. This is an amazing development in the fight against ALS, and a meaningful win for the entire ALS community who worked tirelessly to make this happen.

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The ALS Association

@alsassociation

5 years

Thank you @justinsuntron and thank you to your team @BitTorrent , @Tronfoundation , and @BinanceBCF . Proud to partner with you on this beautiful campaign to spread love and raise awareness of ALS/MND. #VoiceYourLove

H.E. Justin Sun 孙宇晨

@justinsuntron

5 years

Proud to support the @alsassociation ! Let's voice our love, raise money and awareness to help find a cure. #VoiceYourLove @Tronfoundation @BitTorrent @BinanceBCF

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The ALS Association

@alsassociation

4 years

Our hearts go out to Frates family and Boston community. @PeteFrates3 changed the trajectory of ALS forever and showed the world how to live with a fatal disease. His efforts to lead the Ice Bucket Challenge had a significant impact on the search for treatments and a cure for ALS

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The ALS Association

@alsassociation

2 months

Hugh Hoffman wanted to help ensure more children don’t have to lose a parent to ALS. His historic $58 million gift will advance more clinical trials, expand clinic access, and provide some financial support for people living with ALS. Learn more here:

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The ALS Association

@alsassociation

6 years

We’re on our way to growing the Carmen Schentrup ALS Research Fund to 20x Carmen’s initial gift of $5628.84! Won’t you join us in Carmen’s quest to find a cure for #ALS ? Donate here: #CarmensDream #ALSresearch #MSDstrong

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The ALS Association

@alsassociation

6 years

We'd like to extend a special thanks to @terrellowens for his recent donation in memory of Dwight Clark. Thank you for raising awareness for #ALS and vital funds for #ALSResearch , #ALSCare & #ALSAdvocacy through your recent collaboration with @Represent .

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The ALS Association

@alsassociation

2 years

(1/2) BREAKING NEWS: Thanks to the tireless work of #ALSAdvocates across the country, the U.S. Senate just PASSED the #ACTforALS Act! This is a giant milestone in accelerating access to promising treatments for #ALS and to find urgently needed new treatments.

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The ALS Association

@alsassociation

7 years

BREAKING #ALS NEWS! @US_FDA approved 1st new drug for ALS in 22 yrs! We applaud FDA for swift approval of Radicava

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The ALS Association

@alsassociation

6 years

Incredible! Donors continue to match Carmen's original gift of $5,628.84. We're getting close to reaching our goal & EVERY dollar counts! From us & Carmen's family, THANK YOU for supporting #CarmensDream of finding a cure for #ALS ! Donate here: #MSDStrong

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The ALS Association

@alsassociation

6 years

Happy 61st birthday to former @49ers player @DwightC87 ! He’s bravely fighting #ALS and we wish him the best.

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The ALS Association

@alsassociation

2 years

(1/3) BREAKING: @US_FDA ’s Advisory Committee voted 7 to 2 for recommending approval for #AMX0035 . We applaud and thank the FDA Advisory Committee for their vote to support approval of AMX0035 and we urge the FDA to swiftly approve. Americans living with #ALS cannot wait.

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The ALS Association

@alsassociation

10 years

Thank you for your generosity! To date, we have received $88.5 million in donations - http://t.co/KnsYarLxfZ. #IceBucketChallenge .

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The ALS Association

@alsassociation

1 year

(1/2) Another victory for the ALS community! Tofersen is the second treatment approved for ALS in less than a year and the third since 2017. This gene-based therapy is approved for treating people living with SOD1-ALS. Thanks to the entire community for your advocacy!

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The ALS Association

@alsassociation

6 years

The Carmen Schentrup ALS Research Fund has grown by more than 10x! We & Carmen's family are so grateful & humbled at the outpouring of support for #CarmensDream . Our new goal is $112,576.80. Help support the most promising #ALSresearch : #ALS #MSDstrong

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The ALS Association

@alsassociation

3 years

@SurvivorPenner So terribly sorry to hear this news, Jonathan. She was a magnificent warrior against ALS, as are you. You and your family have our deepest condolences.

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The ALS Association

@alsassociation

4 years

We join the ALS community in mourning the loss of the legendary Hollywood publicist Nanci Ryder. #TeamNanci brought together a powerhouse team of friends including Renée Zellwegger, Courtney Cox, and Reese Witherspoon to lead the fight against #ALS .

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The ALS Association

@alsassociation

2 years

@BrainstormCell People living with ALS need new treatments now. We are excited that BrainStorm intends to apply for approval of NurOwn. We continue to encourage BrainStorm to file its application as soon as they are ready, and for @US_FDA to review the application as quickly as possible.

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The ALS Association

@alsassociation

4 years

Today @alsassociation and @IAMALSorg announced that they have awarded $500,000 to @BrainstormCell to support ALS biomarker research and to study how NurOwn works in the body. #ALS #ALSResearch

The ALS Association, I AM ALS Award BrainStorm Cell Therapeutics $500,000 for ALS Biomarker Study

/PRNewswire/ -- The ALS Association and I AM ALS announced today that the organizations have awarded a combined grant of $500,000 to BrainStorm Cell...

www.prnewswire.com

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The ALS Association

@alsassociation

10 years

Learn about global #alsresearch that we are funding. #StrikeOutALS http://t.co/F3VZ1OM2Ue

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The ALS Association

@alsassociation

9 years

The buckets are here and ready for @RedSox ! #ALSIceBucketChallenge #EveryAugustUntilACure http://t.co/McZlyDZpuC

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The ALS Association

@alsassociation

5 years

We're excited to share the news that we have made a $1 million investment into the Phase I trial of AT-1501, a potential ALS therapy developed by @ALSTDI . Anelixis Therapeutics announced the first person received AT-1501 today. 1/3

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The ALS Association

@alsassociation

7 years

Thank you for meeting with your constituents living with #ALS , @SpeakerRyan , and hearing their stories during #ALSHillDay17

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The ALS Association

@alsassociation

6 years

Thanks to the leadership of Steve Gleason & the support of advocates across the country, the Steve Gleason Enduring Voices Act is permanent! We were proud to play a part in advocating for this important piece of legislation! Read more: #ALS @TeamGleason

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The ALS Association

@alsassociation

5 years

It's Valentine's Day! Help us spread a lot of love & #ALSAwareness today. Compared to the immense challenge of living with #ALS , this is so, so easy. Be like Courteney & #VoiceYourLove for someone or something important to you. #MND

Courteney Cox

@CourteneyCox

5 years

When was the last time you told someone you love them? Today we’re launching the Voice Your Love campaign to raise awareness about #ALS and bring a little more love into the world. @alsagoldenwest #VoiceYourLove

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The ALS Association

@alsassociation

4 years

Former @Saints player and #ALS advocate, @SteveGleason , will receive the Congressional Gold Medal today. We are so proud of Steve and all the great work that @TeamGleason does for #OurALSCommunity . Please join us in congratulating him on this special day!

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The ALS Association

@alsassociation

7 years

Hundreds of patients are gathered in the halls of the U.S. Senate to oppose #GrahamCassidy at today's Senate Finance Committee hearing

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The ALS Association

@alsassociation

4 years

Today we are announcing a $3M commitment ($1M/yr for 3 yrs) to @MGHNeurology to support the first ever platform trial for #ALS . Read more:

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The ALS Association

@alsassociation

2 years

We are deeply saddened by the loss of @sandymorris333 . She was a fierce advocate, a devoted mother and wife, and a friend to the entire ALS community. We are thinking of her family and are grateful for her impact in the fight to end ALS.

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The ALS Association

@alsassociation

6 years

We're excited to support @Brewers catcher @JacobNottingham in his mission to #StrikeOutALS in memory of his aunt & grandmother & the many others who've lost their lives to #ALS . Good luck in this afternoon's game, Jacob! #OurALSCommunity

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The ALS Association

@alsassociation

7 years

We’re proud to partner with @MLB to honor @PeteFrates3 by tackling the high cost of #ALS health care! #MLBFightsALS

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The ALS Association

@alsassociation

4 years

In response to the results of the #AMX0035 phase 2 trial published today, @alsassociation and @iamalsorg launched a petition urging @AmylyxPharma and @US_FDA to get the drug to market as soon as possible. Sign today at #ALS #ALSAdvocacy #OurALSCommunity

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The ALS Association

@alsassociation

3 years

BREAKING: The Senate just passed a resolution to make May 2021 #ALSAwareness Month! @ChrisCoons and @SenatorBraun know that #EveryMomentMatters for people with #ALS and their loved ones. We thank them and all Senate #ALS champions for joining our fight to end ALS.

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The ALS Association

@alsassociation

5 years

Today is the 80th Anniversary of Lou Gehrig's farewell speech. Lou raised awareness of a disease that was virtually unknown at the time and made him the face and name of #ALS for decades to come. Read more: #MND #ALSAwareness #LouGehrig

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The ALS Association

@alsassociation

4 years

We are fighting to change the world for the entire ALS community! Special thanks to @iamalsorg and everyone who braved the rain in Times Square today to raise awareness for ALS! #CuresforAll #OurALSCommunity

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The ALS Association

@alsassociation

5 years

It is with heavy hearts that we share that Stephen Winthrop, Chair of The ALS Association Board of Trustees and person with ALS, died peacefully early this morning. Our hearts are with his wife, Jane, and their two daughters.

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The ALS Association

@alsassociation

1 year

Congratulations #SDSU Aztecs on your win tonight and best of luck in the national championship game! Thank you for all you do to help raise awareness of #ALS . #FinalFour

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The ALS Association

@alsassociation

6 years

“The Ice Bucket Challenge was the beginning of ending #ALS ,” - Patt Quinn. Read more about how three years later, we are beginning to see the tremendous payoff of the #ALSIceBucketChallenge :

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The ALS Association

@alsassociation

3 years

⚾ Today is #LouGehrigDay ! Thank you to @MLB , the #ALS community, and the Lou Gehrig Day Committee who made this #ALSAwareness day possible. Learn more:

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The ALS Association

@alsassociation

3 years

HUGE NEWS! The Senate has recommended $40M for the DOD ALSRP and $10M for the CDC National ALS Registry in their FY2021 appropriations bills. THANK YOU to the ALS community and our ALS champions in the Senate for making this happen!

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The ALS Association

@alsassociation

3 years

Thanks to the leadership of ALS champions @SenWhitehouse @SenTomCotton @ChrisCoons & @SenatorBraun , the Senate passed a fix to allow people with #ALS to receive the #SSDI waiting period waiver for applications before Dec. 23. Now the House must act.

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The ALS Association

@alsassociation

10 years

#IceBucketChallenge donations exceed $94 million. Thank you for your support! http://t.co/vLkQPG2lmH

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The ALS Association

@alsassociation

5 years

We're saddened to hear that Stephen Hillenburg, ‘Spongebob’ creator and two-time Emmy winner, has passed away from #ALS at the age of 57. He gave the world a show enjoyed by millions. Our hearts go out to his family & friends. #MND #OurALSCommunity

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The ALS Association

@alsassociation

6 years

We are very sorry to share that Anthony Senerchia, co-founder of #ALSIceBucketChallenge passed away on Saturday. Please see this video to learn more about him and his wife, Jeanette, and how they helped inspire a global phenomenon.

ALS Ice Bucket Challenge Founders: "Every August Until A Cure"

What happened last summer was historic. It started the end of ALS. This August. Every August. Please help us do it again.

www.youtube.com

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The ALS Association

@alsassociation

5 years

We’re so happy to have you voicing your love with us, @CourteneyCox . Thank you! #VoiceYourLove #ALS

Courteney Cox

@CourteneyCox

5 years

When was the last time you told someone you love them? Today we’re launching the Voice Your Love campaign to raise awareness about #ALS and bring a little more love into the world. @alsagoldenwest #VoiceYourLove

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The ALS Association

@alsassociation

1 year

BREAKING! After our repeated requests to discuss their refusal to cover Relyvrio, Cigna has agreed to meet with us. We will keep you posted.

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The ALS Association

@alsassociation

2 years

(1/5) AMAZING NEWS! If you took the Ice Bucket Challenge, you helped deliver AMX0035, the first newly developed treatment approved for ALS in years! THANK YOU! AMX0035 slows progression of ALS and extends life for people living with ALS.

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The ALS Association

@alsassociation

4 years

The House has approved two key appropriations: $10M to the CDC Registry and $20M to the DOD ALS Research Program, doubling funds available to understand the increased risk of ALS for veterans. Deep gratitude to #OurALSCommunity for your tireless #ALSAdvocacy !

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The ALS Association

@alsassociation

2 months

Thank you to Majority Leader @SenSchumer for meeting with the @alsassociation and #ALS advocates today to discuss increasing ALS research funding and passing the #ALSBetterCareAct ! #ALSAdvocacy #FundALSResearch

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The ALS Association

@alsassociation

3 years

A new provisional approval pathway that will accelerate access to promising new treatments is urgently needed. Thank you @RepWesterman , @RepGallagher , @RepMikeQuigley , & @RepSwalwell for reintroducing the #PromisingPathwayAct in the House and supporting people with #ALS .

Rep. Bruce Westerman

@RepWesterman

3 years

Today, I reintroduced the Promising Pathway Act with @RepGallagher , @RepMikeQuigley , and @RepSwalwell to: ✅Cut red tape to bring therapies for terminal patients to market faster ✅Spark competition between small and large pharma companies Learn more👇

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The ALS Association

@alsassociation

9 months

We are saddened to hear of the passing of Bryan Randall. Our hearts go out to his friends and family.

People

@people

9 months

Sandra Bullock's Longtime Partner Bryan Randall Dead at 57 After Private 3-Year Battle with ALS

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The ALS Association

@alsassociation

3 years

Thank you @POTUS for supporting the ALS community by joining our #ALSChampions in Congress and signing the fix to the ALS Disability Insurance Access Act. Your support means all people living with #ALS can immediately access their #SSDI benefits. Read more

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The ALS Association

@alsassociation

4 years

Congratulations to #ReneeZellweger for taking home Best Actress at #Oscars2020 for her amazing performance in @Judy . Renée is a huge #ALS advocate, helping raise awareness and donations. We are thrilled for Renée and thank her for being part of our fight.

Renée Zellweger - #VoiceYourLove

#VoiceYourLove is a campaign to raise awareness for ALS and one of its many debilitating symptoms: losing the ability to speak.We’re on a mission to uncover ...

www.youtube.com

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The ALS Association

@alsassociation

2 years

Our hearts are with Margot and her loved ones as she faces this devastating disease. Thank you, @StarTrek community, for your support in her fight against #ALS !

Jeri Ryan

@JeriLRyan

2 years

My dear friend Margot needs our help. Please click the link to donate at and RT this video to spread the word! 🖖🏼❤️ #trekagainstals

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The ALS Association

@alsassociation

5 years

The ALS Association, ALS Finding A Cure, and @MDAorg award a $2.5 million clinical trial grant to study novel #ALS therapy. This fundingwill allow Dr. Appel to expand the first-in-human study that demonstrated promising results. Read more: #ALSresearch

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The ALS Association

@alsassociation

6 years

We were sad to hear about Dwight Clark's passing this evening and send our condolences to his loved ones. #ALS #MND #OurALSCommunity

49ers hero Dwight Clark dies at 61 after battling ALS

Dwight Clark announced he had ALS in March 2017.

www.si.com

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The ALS Association

@alsassociation

7 years

We are honored to be partnering w/ @MLB for #MLBFightsALS ! Read more here and stay tuned for details! #strikeoutALS

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The ALS Association

@alsassociation

9 months

It is with heavy hearts that we share that our colleague Jeremy Holden, host of our Connecting ALS podcast, passed away earlier this week. Jeremy had been with us since 2017 and was truly dedicated to our cause and the ALS community. He was also a well-respected colleague and…

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The ALS Association

@alsassociation

4 years

In his farewell speech, #LouGehrig called himself the luckiest man on the face of the earth. He wasn’t thinking of himself, but rather thanking those who had helped him in life. Tomorrow is Lou's birthday. Read more about his legacy & courage: #ALS

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The ALS Association

@alsassociation

5 years

(1/2) Carmen Schentrup dreamed of becoming a medical researcher & focusing on a cure for #ALS . Her life was tragically cut short in last year's horrific Parkland shooting. However, #CarmensDream to contribute to a cure is still being realized in a significant way. #ALSResearch

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The ALS Association

@alsassociation

8 years

The #IceBucketChallenge impact grows as researchers identify one of the most common gene contributors to #ALS

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The ALS Association

@alsassociation

4 years

We are excited to endorse the Promising Pathways Act - announced by @SenatorBraun at the #ALSAdvocacy Conference - to create a faster pathway for new therapies.

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The ALS Association

@alsassociation

2 years

Thank you to @IAMALSorg , @MDAorg and the many passionate advocates with #ALS who partnered to pass the #ACTforALS Act. This is an historic moment that will directly impact the lives of people with #ALS .

U.S. Senator Christopher Coons of Delaware

The Official U.S. Senate website of Senator Christopher Coons of Delaware

www.coons.senate.gov

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The ALS Association

@alsassociation

9 years

July 4 1939: #LouGehrig 's speech brings national attention to #ALS . His words continue to inspire. http://t.co/fhlz85mDoo

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The ALS Association

@alsassociation

3 years

HUGE #ALSAdvocacy News: the U.S. House of Representatives PASSED the ALS Disability Insurance Act! Thanks to the tireless work of ALS advocates & House champions this 4 year fight for immediate access to #SSDI benefits for people with #ALS is almost over.

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The ALS Association

@alsassociation

4 years

This month we're helping create broader awareness of ALS worldwide. Please share this post with your social network build an even larger and more powerful community of people working together to find effective treatments and a cure. #ALSInThisTogether #ALSAwarenessMonth

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The ALS Association

@alsassociation

7 years

This year, Walks to Defeat ALS raised more than $24 million to support the #ALS community. Thank you for being a part of #OurALSStory

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The ALS Association

@alsassociation

6 years

Steve Gleason is being considered for the Congressional Gold Medal in recognition of his work through the Gleason Initiative Foundation. To show your support, contact your Congressional leaders. #ALSAdvocacy #OurALSCommunity #NoWhiteFlags @TeamGleason

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The ALS Association

@alsassociation

7 years

“It is refreshing to see rival Duke and UNC basketball coaches come together to fight ALS” – Dr. Bedlack, @DukeU #ALS Clinic.

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The ALS Association

@alsassociation

3 years

People living with #ALS urgently need effective new treatments. The reintroduced #ACTforALS Act will help us reach this goal. That’s why we’re joining @iamalsorg and @MDA_Advocacy to call on Congress to support and pass the ACT for ALS Act now. Read more:

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The ALS Association

@alsassociation

6 years

#ALS is incurable, but only for now. Scientists are going all-in to find a cure, and they’re making big progress. New technology, new discoveries, and new research are starting to make a difference:

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The ALS Association

@alsassociation

10 years

It's literally "soaked" the nation...the #IceBucketChallenge . #StrikeOutALS http://t.co/ruuyt83Ymr

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The ALS Association

@alsassociation

4 years

We can’t wait until this is over to find a cure for ALS. Please visit today and find out how we can end ALS together. #WeCantWait #ALS #ALSawareness

When This is Over

alscantwait.org

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The ALS Association

@alsassociation

5 years

“There will be a cure for ALS and it won’t be in the distant future.” -Don Cleveland, Ph.D. #ALS #MND #ALSResearch #ChallengeMe #ALSIceBucketChallenge

2019 Challenge Me - Dr. Cleveland

null

www.youtube.com

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The ALS Association

@alsassociation

7 years

This is a very important day in the fight against ALS. You can learn more about the new drug at .

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The ALS Association

@alsassociation

5 years

It is with heavy hearts that we share the news that Ryan Farnsworth, whose story is featured as a part of our #VoiceYourLove campaign, died yesterday evening surrounded by his family. #ALS #MND #OurALSCommunity

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The ALS Association

@alsassociation

2 years

(1/2) BREAKING: The #ACTForALS Act has been signed into law. Thank you to all #ALSAdvocates for the hard work it took to get this historic bill across the finish line. Thank you @POTUS for supporting people with #ALS & their loved ones. Your tireless support makes a difference!

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The ALS Association

@alsassociation

5 years

Great news! The Senate has taken the first step toward doubling funding for #ALS research at the DOD, from $10M to $20M. The House has already approved and now the full Senate must approve. We thank ALS advocates and our ALS champions in Congress. /1

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The ALS Association

@alsassociation

2 years

Today @alsassociation , @iamalsorg and @MDAorg are calling on Congress to fully fund the #ACTforALS Act and increase investments in #ALS research programs at @DeptofDefense , @NIH and #ARPA -H. Read our joint statement:

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The ALS Association

@alsassociation

3 years

(1/5) The @US_FDA has agreed to the ALS Association’s urgent request that they hear directly from people with ALS about their willingness to accept the risks of promising experimental therapies.

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The ALS Association

@alsassociation

5 years

Every 90 minutes, someone is diagnosed with #ALS & someone passes away from ALS. And 5,000+ people are diagnosed each year. Greater #ALSAwareness & more #ALSResearch are needed. Won't you help by retweeting or making a donation?

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The ALS Association

@alsassociation

5 years

There aren't enough words to express our gratitude for the family members who care for loved ones with #ALS every day. Thank you so much, caregivers! You're amazing. Watch our special video: . #MND #ALSCare #OurALSCommunity #NationalFamilyCaregiversMonth

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The ALS Association

@alsassociation

4 months

It is with heavy hearts that we share @adamfwilson426 , one of the founders of the @LG4Day Committee, has passed away. Adam inspired @MLB and its teams to create Lou Gehrig Day and united the #ALS community to celebrate it. He was a great friend and devoted father to Avery. Our…

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The ALS Association

@alsassociation

3 years

(1/3) BREAKING: After further conversation with the @US_FDA , we have secured its consent to livestream the We Can’t Wait Action meeting on May 25 at 10am ET.

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The ALS Association

@alsassociation

7 years

You can help continue lead the fight to treat and cure ALS by making a contribution on #GivingTuesday . Learn more: .

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The ALS Association

@alsassociation

4 years

More good news from Congress: the Senate approved $20M for @DeptofDefense ALS Research Program (ALSRP), $41.7B for @NIH , and $10M for @CDCgov 's National #ALS Registry. Thanks #ALSAdvocates from across the country for fighting to protect and increase this critical research funding

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The ALS Association

@alsassociation

2 years

Breaking news!

Amylyx

@AmylyxPharma

2 years

We are excited to share that the FDA has accepted for priority review the New Drug Application (NDA) for AMX0035 for the treatment of #ALS .

19

59

247

1

22

67

The ALS Association

@alsassociation

9 years

Happy Birthday #LouGehrig ! http://t.co/q2S9YwiuFy

0

70

60

The ALS Association

@alsassociation

5 years

The Stephen Michael Gleason Congressional Gold Medal Act (S.2652) just passed the House! We were honored to support this important initiative to #HonorGleason . #ALS #MND #OurALSCommunity

0

16

61