Live Like Lou @LiveLikeLou4
Leaving ALS better than we found it #ONWARD #LiveLikeLou livelikelou.org Joined March 2013-
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It’s ALS Awareness Month!Come join me, @RoseannHickma15 @sperokoulouras and Wendy Faust tomorrow, May 6th at 12 pm CST for a free virtual lunch and learn on Lou Gehrig and ALS. Registration 👇 @Iamals, @LiveLikeLou4, @jonathaneig, @Shankapotomas @KickenALSAss @LorrisPodcast
It’s ALS Awareness Month!Come join me, @RoseannHickma15 @sperokoulouras and Wendy Faust tomorrow, May 6th at 12 pm CST for a free virtual lunch and learn on Lou Gehrig and ALS. Registration 👇 @Iamals, @LiveLikeLou4, @jonathaneig, @Shankapotomas @KickenALSAss @LorrisPodcast
#alsAwarenessMonth Did you know that baseball was Lou's SECOND sport? ⚾ The Iron Horse attended Columbia University on a football scholarship to study engineering! #livelikelou #als #alsawareness #lougehrig
#alsAwarenessMonth Lou's streak ended due to complications with ALS. Battling a slump with his weakened body, Lou played the 2,130th consecutive game of his career on April 30, 1939. It was also his final game in the majors. #livelikelou #als #alsawareness #lougehrig
The great Lou Gehrig took himself off the Yankees lineup on May 2, 1939. Several months later, he would give his infamous speech declaring himself the “luckiest man.” Today, I am joining @LiveLikeLou4 in wearing #blue4Lou Do it for the Iron Horse. livelikelou.org/als-families
The #Blue4Lou posts are rolling in and we love to see it! 💙 Thank you for honoring your loved ones and helping to spread ALS awareness today, and always. #livelikelou #lougehrig #fightals #endals #strikeoutals #ALSawareness
Join us at Target Field on Tuesday, June 11, for the @Twins' #LouGehrigDay game against the @Rockies. ⚾ Carlos Correa is a finalist for the #GehrigAward, and a local ALS family will be honored. Tickets: phide.lt/3xSbX4o #LG4Day #livelikelou #ALSawareness
Join Live Like Lou and our friends from @Iamals on May 6 for an informative webinar on Lou Gehrig and ALS. Learn more and sign up to attend this free event here: grayslake.librarycalendar.com/event/lunch-an…. Don't wait; there are only 86 open spots remaining! #livelikelou #als #alsawareness
Thank you @ALSTDI for an incredible discussion and tour this morning highlighting your work in ALS drug discovery and scientific research! We are thankful to partner in the quest to #endALS together. #livelikelou #alstdi #ALSresearch #lougehrigsdisease
Great night at @fenwaypark celebrating @BCBirdBall pitcher @johnny_west13 and surprising Jim Duhamel with a @PermobilCares wheelchair! ⚾️🦅 #ALSawareness #livelikelou #lougehrigsdisease #bcbirdball #strikeoutALS
We're now on Roon! Watch short videos of industry leaders, caregivers, & people living with ALS answering ALS questions. Our Executive Director, Wendy Faust, is featured and answers questions about #LiveLikeLou! Checkout the videos here: roon.com/als/experts/we… #als #alsawareness
I was honored to represent @LiveLikeLou4 at the Chapman Phi Delta Theta Sword & Shield Banquet by sharing my lived #ALS experience + the impact that LLL's Connect & Serve program has for ALS families like mine. Learn more about Connect & Serve via the link in the comments⚡️
Join us, @phideltatheta, & @PermobilCares at Kauffman Stadium on June 2 for the @Royals' #LouGehrigDay game against the @Padres. ⚾ Before the game, there will be a special presentation to an ALS family. Tickets: givebutter.com/Royals24?utm_c… #LG4Day #livelikelou
Join us at PNC Park on Tuesday, June 4, for the @Pirates' #lougehrigDay game against the @Dodgers. ⚾ Before the game, a local ALS family will be honored. Get tickets: givebutter.com/Pirates24?utm_… #livelikelou #als #lougehrig #lougehrigsdisease #mlb #baseball #LG4Day
It's #volunteerappreciationWeek, and we're shouting out all the incredible Connect and Serve volunteers who have dedicated their time and hearts to serving ALS families! Thank you for your work to leave ALS better than you found it! 💙 #livelikelou #als #volunteerappreciation
Join us at Great American Ballpark on Sunday, June 9, for the @Reds' #LouGehrigDay game against the @Cubs. ⚾ Hunter Greene is a finalist for the #GehrigAward, and a local ALS family will be honored. Tickets: givebutter.com/reds24?utm_cam… #LG4Day #livelikelou #ALSawareness
Join us at Truist Park on Sunday, June 2, for the @Braves' #LouGehrigDay game against the @Athletics. ⚾ Matt Olson is a finalist for the #GehrigAward, and a local ALS family will be honored. Tickets: givebutter.com/Braves2024?utm… #LG4Day #livelikelou #ALSawareness
⚾ Join us on 4/25 for Boston College's annual ALS Awareness Game. @BCBirdBall pitcher John West will be honored & an ALS family will receive a special surprise. Purchase tickets in our block here: givebutter.com/2024communityi… #livelikelou #als #bostoncollege #baseball
Leanne Yacyshyn @leanne_yacyshyn
9K Followers 1K Following Wife. Mom of 2 teens. Former elementary school teacher. Canucks fan. Living with ALS and waiting for the day it is no longer terminal.Sandra W. Marlowe @sandrawmarlowe
3K Followers 1K Following Married to the love of my life. Christ follower. Mom of five. Mimi to 14! Entrepreneur. Diagnosed with Bulbar ALS 3/30/2020. Fighting to live.Sandra Abrevaya @sabrevaya
21K Followers 4K Following Wife to @bsw5020. Mama to spunky girls. Caregiver. CEO & Co-founder @synapticure. Co-founder @iamalsorg. Executive Producer @noc_film. All in on curing ALS.ALS Advocacy @alsadvocacy
12K Followers 2K Following ALS = Lou Gehrig's Disease Thought it had been cured by now? Still no known cause. Still no cure. Still no treatment. Still quickly fatal. Still outrageous.AZ Latina ☮️🌊�.. @aVoice4ALS
4K Followers 5K Following Political Junkie. Advocate for Enviro Justice, Foster Care, Gun Safety, DEI, Amyloidosis, PD, ALS & Rare Diseases. Love LA Sports. I block disrespectful people.Jamie Smith @JamieLW8
4K Followers 567 Following Mother I Widow I Pediatric Respiratory Therapist Fighting for reform in health care and research for ALS.Seth Poling @SethPoling10
5K Followers 392 Following Wild & Wonderful WV. FSU grad. Married to @erika_poling , Father to Liam & Bayler, ALS Warrior & advocate. #EndALS Founder of @project_sethSarah Nauser @SarahNauser
12K Followers 518 Following Dominating ALS one day at a time. “Love the life you live and live the life you love” Go Royals! #FightLikeAGirlMandi @RunningMama0522
2K Followers 1K FollowingALS Uncensored 🏴�.. @ScottsFight
2K Followers 1K Following Scott Craig. ALS Uncensored podcast. Digital Artist. AI Student. Typing with my eyes. Living Impossible! #ALSUncensored #ALS #EyeGazeArtist #AI #IWriteALSEnd ALS Now @EndALSNow
961 Followers 935 Following ▪Bri ▪I mainly amplify #ALS tweets ▪ALS=wretched, cruel, 100% fatal ▪RT=awareness, not agreement ▪🚫DMs🚫 ▪#EndALS ▪#SunflowerForSandy 🌻 ▪#RoseForJamie 🌹Lisa's Legacy for ALS @LisaLegacy4ALS
2K Followers 910 Following Lisa Stockman Mauriello fought for Expanded Access to an ALS treatment. Lisa passed away 8.4.21. Honor Lisa’s legacy by advocating for change for ALS.Dr. Nadia Sethi @nadia_sethi
2K Followers 2K Following Director, Community Outreach and Engagement at ALS TDI. ALS we are coming for you. Widowed by ALS and still fighting it. Views expressed here are my own.SOD1 EndALS @CEHaddadNP
2K Followers 2K Following #ALS #fALS #SOD1 In the fight to save my family from ALS. Twin mom. Nurse practitioner. grieving daughter - 8/30/22 lost mom #33 in our familyALS ACCESS @brainmatters10
2K Followers 2K Following Fighting for a cure for ALS/MND/ and it’s variants. Fighting daily for many years, for ALS drug access. Sod1 Gene carrier.Shah Minokadeh, M.D. @MinoShah
4K Followers 740 Following Anesthesiologist -Johns Hopkins Hospital Pain Management -UC San Diego Now battling ALS & FDA regulatory rigidity for 100% fatal ALSI’m Dying To Tell Y.. @LorrisPodcast
1K Followers 870 Following Midwest Momma & Wife. ALS Warrior for 20 years. Host of I’m Dying To Tell You Podcast. Living Faith Over Fear. Instagram: imdyingtotellyoupodcastLyn Bussells @LBussells
16 Followers 206 FollowingMichele Dupree @KickALS
1K Followers 1K Following #ALS advocate. Fighting for your life is a human right. I’m a believer in letting people choose their risks. Hands off.Jason Ford @JasonFord6
604 Followers 2K Following Executive Search: Biotech, Pharmaceuticals and patient focused nonprofits. We help our partners hire transformational leadership to drive cures and therapies.Watching @lauhal
22 Followers 371 Following I don’t do the follow back thing, so I remove most followers . 🤷🏻♀️Much love, though. ❤️wanderer @ahsihr
142 Followers 761 Following Every man has two lives, and the second starts when he realizes he has just one - ConfuciusCarol Hamilton @chamtdi
420 Followers 553 Following Fighting ALS while loving the people who live with it. All thoughts and tweets are strictly my own.Aggedy Ann @aggedy_ann
500 Followers 441 Following Nurse/ CWOCN/ MSCJ/ Pterodactyl/ Remaldog’s mom/ She/her/ Never stop fighting til the fight is done/ Change what you cannot accept.We Will Cure @cure345
114 Followers 64 Following Cure’s mission is to foster & accelerate critical conversations around the future of healthcare and medicine, so we can Cure, period!gemofhighlands @gemofhighlands
6 Followers 60 Following✈️ John Jetson�.. @ganggreen82
2K Followers 5K Following Family man & life-long, die-hard Jets fan✈️#TakeFlight #AGNB⛽️ RU🏈🏀#CHOP🪓 NYY⚾️ #RepBX Rock🎸 Here for sports, entertainment, & anything interesting #EndALSBrian Donovan @CheckBd
10 Followers 77 Following Diagnosed with ALS in 2024, but embracing hope. A proud husband, dad, and granddad, believe in future breakthroughs and cherish every family moment.Jonathan Brent M.D., .. @DrJBrent
277 Followers 1K FollowingJC @JC75408607
563 Followers 457 Following Diagnosed with ALS 3/30/22. Living life day by day while I try and process this journey.Joseph Williams @jjosephwilliams
2K Followers 3K Following Son of God. Husband of @palmerhwilliams. Father of Jack, Henry, and Teddy. Lover of People, Sports, Film, & TV. Constitutional Lawyer.HonorableAnyone @WinThymeAgain
109 Followers 855 FollowingJoin Team Mia! @join_team_mia
85 Followers 51 Following We are the family and friends of Mia Costanza Wiggers, taken by ALS in March 2023, supporting other pALS and their familiesLaurel Boyle @LaurelB24095476
0 Followers 33 FollowingCasey H @CaseyHerd
3K Followers 4K Following Traveling around the world with @BalletRising 🩰 & fighting #ALS alongside my sister ❤️Kevin Geraghty @KevinMGeraghty
241 Followers 354 Following 40 year old hell bent on living and fighting #ALS with every fiber of my being. If you’re going through hell, keep going. #IAMALS #EndALS #fuckALSAnne Chen @AnneChenNeeNee
11 Followers 125 Following Active life, career, cheerful and optimistic personalityDeb Paust @PaustDeb
1K Followers 727 Following Blessed mom, lover of snow, I AM ALS Organizing Associate, old fashion enthusiast and trying to be the change I wish to see in the world. #GoodTroubleM.A Ly @anh_ma_ly
12 Followers 81 Following PREP Scholar at @MayoClinic @RossollLab | Neuroscience 🧠🥼👩🔬 | us-based, saigonese, views my own (she/her)Fergal Waldron @FergalWaldron
441 Followers 487 Following Advanced Research Fellow @aberdeenuni | MND/ALS & neurodegenerative diseases | Clinical heterogeneity | Immunity & neuroinflammation | Genetics | Data synthesisOlivia Rifai @olivia_rifai
263 Followers 332 Following TL1 postdoc fellow at @ColumbiaMed 🔬 formerly at @EdinUniNeuroC Lewis @cml86
2 Followers 2K FollowingTarget ALS @TargetALS_fdn
2K Followers 525 Following Target ALS brings together the right people, funding, critical tools and resources to foster the creation of breakthrough therapies to treat people with ALS.Ashley Thombs @athombs
301 Followers 417 Following The past is prologue to a future. What it will be, I don’t know. END ALSEmily Mayberry (she/h.. @ejmayberry
339 Followers 516 Following Clinical Psychologist & Researcher | PhD, DClinPsy | 🇺🇸🇬🇧🌏 | focus: MND/ALS; improving psychological care and quality of life for all affected | views mineBeth Gabel @beth_gabel_27
75 Followers 53 Following #ALS warrior. Mom of 2 teenage boys. Diagnosed April 2023. ALS advocate and mentor. Love heavy metal music, painting and natureTravis Lane @travislane20
339 Followers 321 Following Phillips Academy '18 | Boston College Baseball #45|Cameron Krebs @CamKrebsvball
45 Followers 229 Following #11 | WHS | 2025 | DS/L,OH| 3 sport varsity athlete| 4.15 GPAJay Piwnicki @jaypiv
63 Followers 74 Following All we need is common sense. That and a cure for ALS.Wayne State Baseball @waynestbaseball
7K Followers 989 Following Home of Wayne State University Baseball. Visit us at Harwell FieldDanny Corona @CoachDCorona
2K Followers 3K Following Scout - NY @Yankees. Father of 2 Amazing boys - Danny Jr & Shea. @metroscoutday 🗽🌃Michael Meals @Otown334
886 Followers 3K Following The Lord your God is in your midst, a mighty one who will save; He will rejoice over you with gladness; He will quiet you by His love... Zephaniah 3:17Shawn Lyons @Shawnl8
463 Followers 156 Following father, husband, runner, elementary school principal, & still just a kidDaniel Hale @DanielH03274759
188 Followers 276 Following Foremost ALS Research in the world. ALS recovery from complex reactive species trigger and biophysics cause. Formerly 3000 followers.Tavares Speer @TavaresSpeer
449 Followers 207 Following Husband, Dog Dad, Former Business Analyst & FSU Alum. I was dx w/ #als 10/4/18. Still fighting. #alsfighter #alsawareness #EndalsBecky Spratford (she/.. @RAforAll
5K Followers 3K Following Matching books w/ readers thru the library esp Horror. Jersey Girl in exile. @AmherstCollege '97 P'24. @BlairSchool P'27. @HorrorWriters Sec. Rep @LaneHeymontGhazy Saab🇱🇧 @ghazy_saab
8K Followers 3K Following الحكماء يتكلمون لأنّهم يملكون شيئاً لقوله ..أمّا الحمقى فيتكلمون لأنّ عليهم قول شيء وحسب.Brian Wallach @bsw5020
159K Followers 3K Following Dad, husband, activist, entrepreneur, unlikely movie star, living with ALS, a currently fatal disease.Kelsie Snow @kelsieswrites
61K Followers 1K Following Storyteller, writer, podcaster @sorryimsadpod, ALS advocate, widow, mom, dual citizen (🇨🇦🇺🇸). Instagram & TikTok: kelsieswritesLeanne Yacyshyn @leanne_yacyshyn
9K Followers 1K Following Wife. Mom of 2 teens. Former elementary school teacher. Canucks fan. Living with ALS and waiting for the day it is no longer terminal.Sandra W. Marlowe @sandrawmarlowe
3K Followers 1K Following Married to the love of my life. Christ follower. Mom of five. Mimi to 14! Entrepreneur. Diagnosed with Bulbar ALS 3/30/2020. Fighting to live.I AM ALS @iamalsorg
26K Followers 799 Following I AM ALS is a patient-led movement revolutionizing how to end disease with our sights set squarely on ALS.Sandra Abrevaya @sabrevaya
21K Followers 4K Following Wife to @bsw5020. Mama to spunky girls. Caregiver. CEO & Co-founder @synapticure. Co-founder @iamalsorg. Executive Producer @noc_film. All in on curing ALS.ALS Advocacy @alsadvocacy
12K Followers 2K Following ALS = Lou Gehrig's Disease Thought it had been cured by now? Still no known cause. Still no cure. Still no treatment. Still quickly fatal. Still outrageous.AZ Latina ☮️🌊�.. @aVoice4ALS
4K Followers 5K Following Political Junkie. Advocate for Enviro Justice, Foster Care, Gun Safety, DEI, Amyloidosis, PD, ALS & Rare Diseases. Love LA Sports. I block disrespectful people.Jamie Smith @JamieLW8
4K Followers 567 Following Mother I Widow I Pediatric Respiratory Therapist Fighting for reform in health care and research for ALS.Mayuri Saxena @Mayuri_Saxena
9K Followers 607 Following 39yo living with ALS on Life support. Author. Creative Director. Advocate. Dreamer. Public Servant. ALSFRS 1/48 https://t.co/vibJSKdIl4Seth Poling @SethPoling10
5K Followers 392 Following Wild & Wonderful WV. FSU grad. Married to @erika_poling , Father to Liam & Bayler, ALS Warrior & advocate. #EndALS Founder of @project_sethALS TX DAD @AlsDads
2K Followers 893 Following USAF Vet, Father of 4, background in Healthcare Management and Disaster Response Management, ALS (pALS) Advocate (views & comments are my own)Sarah Nauser @SarahNauser
12K Followers 518 Following Dominating ALS one day at a time. “Love the life you live and live the life you love” Go Royals! #FightLikeAGirlMandi @RunningMama0522
2K Followers 1K FollowingSteve Gleason - "Live.. @SteveGleason
199K Followers 252 Following New Instagram - @stevegleasonofficial Dad. Husband. Inspiring all people to live purposefully, despite tragedy. I tweet with my eyes. Embracing ALS.ALS Uncensored 🏴�.. @ScottsFight
2K Followers 1K Following Scott Craig. ALS Uncensored podcast. Digital Artist. AI Student. Typing with my eyes. Living Impossible! #ALSUncensored #ALS #EyeGazeArtist #AI #IWriteALSEnd ALS Now @EndALSNow
961 Followers 935 Following ▪Bri ▪I mainly amplify #ALS tweets ▪ALS=wretched, cruel, 100% fatal ▪RT=awareness, not agreement ▪🚫DMs🚫 ▪#EndALS ▪#SunflowerForSandy 🌻 ▪#RoseForJamie 🌹David Gate @DGateLab
3K Followers 2K Following Assistant Professor, Northwestern Neurology. The Gate lab studies the role of the immune system in neurodegenerative diseases.Dr. Monica M. Bertagn.. @NIHDirector
183K Followers 122 Following Official account of the @NIH Director Posts prior to 11/9/23 were from former NIH Directors Engagement ≠ endorsement Privacy: https://t.co/GijpA0bFOxDonnelly Lab @donnelly_lab
494 Followers 194 Following The Donnelly Lab and LiveLikeLou Center for ALS Research at the University of Pittsburgh. We study the molecular causes of neurodegenerative disease.Manolis Kellis @manoliskellis
25K Followers 4K Following Dissecting disease mechanism. Single-cell, Epigenomics, Regulatory Genomics, Disease Genetics, Brain, Cancer, Metabolism. @MIT Prof, @MIT_CSAIL, @BroadInstituteEurekAlert! @EurekAlert
45K Followers 349 Following Daily trending science news, images, videos, & more. Operated by @AAAS, the world’s largest general science society.Joseph Williams @jjosephwilliams
2K Followers 3K Following Son of God. Husband of @palmerhwilliams. Father of Jack, Henry, and Teddy. Lover of People, Sports, Film, & TV. Constitutional Lawyer.ALS ONE @alsone_official
960 Followers 635 Following Our world leaders in ALS research & care have united 2 advance critical research towards a cure while improving the qual of life of individuals living w/ALS nowGerald McCormick @GeraldMcCormick
1K Followers 245 Following Former House Majority Leader in Tennessee General Assembly. Works for The Ingram Group. Navigating ALS.Kevin Geraghty @KevinMGeraghty
241 Followers 354 Following 40 year old hell bent on living and fighting #ALS with every fiber of my being. If you’re going through hell, keep going. #IAMALS #EndALS #fuckALSLorri Cavaliere @LorriCav
1K Followers 4K Following A mom in CT, fighting and advocating every day for the life of my 32-year old daughter, Alexandra, diagnosed with sporadic bulbar-onset ALS in July of 2020.Ashley Thombs @athombs
301 Followers 417 Following The past is prologue to a future. What it will be, I don’t know. END ALSNeuron @NeuroCellPress
110K Followers 398 Following Neuron publishes ground-breaking research papers, reviews & commentary across neuroscience and is a premier intellectual forum for the neuroscience community.Beth Gabel @beth_gabel_27
75 Followers 53 Following #ALS warrior. Mom of 2 teenage boys. Diagnosed April 2023. ALS advocate and mentor. Love heavy metal music, painting and natureNature Neuroscience @NatureNeuro
409K Followers 268 Following News, commentary and research coverage from the international monthly journal publishing the highest quality of work in all areas of neuroscience.Vanderbilt Baseball @VandyBoys
226K Followers 352 Following 2014 & 2019 NCAA CWS champions. 5 College World Series appearances. 17 straight NCAA Tournaments. #VandyBoys #AnchorDownNancy Frates @momfrates
4K Followers 1K FollowingTavares Speer @TavaresSpeer
449 Followers 207 Following Husband, Dog Dad, Former Business Analyst & FSU Alum. I was dx w/ #als 10/4/18. Still fighting. #alsfighter #alsawareness #EndalsSandra Herron @SandraHerron
119 Followers 170 Following Learner. Culture buff. Enthusiast. Occasional gadfly.Sheri Strahl @sheri_strahl
49 Followers 48 Following President & CEO | ALS Network Working tirelessly to realize positive change through excellence, collaboration, and leadership.Clene Nanomedicine @CleneNano
769 Followers 165 Following Clene is committed to revolutionizing the treatment for people living with neurodegenerative diseases to restore and protect neuronal health.Marilyn @mdemaria2017
662 Followers 249 Following Passionate ALS Advocate. We will be the change for ALS Treatments. “Patients took over & everything changed.” Support I Am ALS. Lover of 🧁Mary Kay Turner @MaryKayTurner1
1K Followers 716 Following Government Affairs | Health Policy| Mom| Dog Lover | Oregon Ducks Fan| Traveler| Defender of Biopharma | Innovation Matters | ALS Advocate| Opinions Are My OwnJeff Lyster @JeffLyster1
3 Followers 2 FollowingMatt Wild @marinemattcda
600 Followers 2K Following Family Man, Husband, former Marine, disabled Vet w/ ALS, Matt's Place Founder, Advocate #Uncrushablespirit, Adaptive Gamer, Escape from Tarkov ADDICTSusan Goldstein @susanhgoldstein
383 Followers 381 Following Pharma/biotech business and communications professional. Mom. Volunteer advocate/family with #ALS aka Lou Gehrig's disease. #EndALS. She/Her/HersPeggy M. Johnson @peggymjohn
592 Followers 579 Following Retired educator. Reader. Traveler. Fan of enthusiastic young people. #endALS #C9orf72Deb Bellina @BellinaDeb
98 Followers 151 Following Lean Six Sigma Black Belt. Matt’s mom, advocating for people living with ALS today and people who will be diagnosed tomorrow, and the next day, and the nextMattsPlaceFoundation @JoinMattsPlace
993 Followers 4K Following Provide accessibility, housing and support to families battling ALS throughout ID, MT & WA #uncrushablespirit #alsGarrett May @rett_may
243 Followers 878 Following Latter-day Saint & disciple of Christ, ALS advocate, BYU Humanities alum, GW Law grad. Immigration lawyer. I think video essays are cool.Allison Brager @docjockzzz
322 Followers 44 Following Neuroscientist. American Soldier. Author of Meathead: Unraveling the Athletic Brain. Crossfit Games Team Athlete.Milken Institute @MilkenInstitute
93K Followers 2K Following Catalyzing Solutions. Building Meaningful Lives. #MIGlobalPete Wallach @pwallach87
1K Followers 2K Following Top 5 cartwheeler in the Midwest*. Opinions are my own. CFO, @Synapticure. YC S20. previously @bainandcompany, @columbia_biz, @uva . #ENDALSALS Hope Foundation @ALSHF
3K Followers 610 Following The mission of the ALS Hope Foundation is to make a difference in the lives of people living with ALS through Care, Research and Education.Tim Lowrey @gatortimbo
453 Followers 639 Following Grateful and blessed to be married to Emily Wester Lowrey, UF Pharmacy '92, Buffalonian, Diehard Gator, Home remodeler, Avid reader of various, living with ALStom miller @molemanz
26 Followers 487 Following Cincinnati Bearcats fan. Diagnosed with ALS in October of 22’Michele Dupree @KickALS
1K Followers 1K Following #ALS advocate. Fighting for your life is a human right. I’m a believer in letting people choose their risks. Hands off.ALSUntangled @ALSUntangled
102 Followers 2 Following Every day more deaths and tortuous suffering. It’s time to stop clowning around with ALS research and those whose lives depend on it. #dyingwaitingTarget ALS @TargetALS_fdn
2K Followers 525 Following Target ALS brings together the right people, funding, critical tools and resources to foster the creation of breakthrough therapies to treat people with ALS.Robert Packard Center.. @packardcenter
2K Followers 668 Following The Packard Center enables the best ALS scientists to collaborate and develop new treatments and find a cure for ALS, also known as Lou Gehrig’s disease.MGH Neurology @MGHNeurology
8K Followers 742 Following On a mission to find new treatments and cures to eliminate the devastating impact of neurological disorders.ALS Canada @ALSCanada
7K Followers 2K Following We work with the ALS community to improve the lives of people affected by ALS through support, advocacy and investment in research for a future without ALS.BrainStorm @BrainstormCell
5K Followers 777 Following BrainStorm Cell Therapeutics, Inc. (NASDAQ: BCLI) is a clinical-stage biotechnology company developing autologous cell therapies for neurodegenerative diseases.Team Gleason @TeamGleason
6K Followers 495 Following Nonprofit founded by former New Orleans Saints player, @SteveGleason, after his diagnosis with Amyotrophic Lateral Sclerosis (ALS) in 2011. NO WHITE FLAGSlori andre @loriandre3
1K Followers 335 Following Mother of 3 boys, wife of Brian Andre who was diagnosed with ALS in 2016.Join us at Target Field on Tuesday, June 11, for the @Twins' #LouGehrigDay game against the @Rockies. ⚾ Carlos Correa is a finalist for the #GehrigAward, and a local ALS family will be honored. Tickets: phide.lt/3xSbX4o #LG4Day #livelikelou #ALSawareness
Sam Hilliard broke the Isotopes HR record last night. Some fun stats below. Longest home run: 494.5 ft. Highest exit velocity: 113.2 MPH Most home runs against: El Paso, 12 Consider donating to his foundation: givebutter.com/StrikeOutALS20… #ALSAwarenessMonth
givebutter.com/StrikeOutALS20… Please give and share to Help fund our efforts for ALS treatments @ALSTDI and supporting families in 2024 @LiveLikeLou4 foundation!! #strikeoutALS
Happiest of birthdays @SlangsOnSports
Birthdays are important!! From your friends and some of your favorite players across MLB, happy birthday, @SlangsOnSports!
May is ALS Awareness Month. I’ll be posting ALS and advocacy information to help raise more awareness about this awful disease. #ALSAwarenessMonth #ALSAwareness #askmeQuestions
Oh my GOODNESS 😭😭😭😭 Thank you so much to EVERYONE involved with this, including the incredible @MLB social squad 🫶 Baseball is the best because its people are the best 💕 And birthdays are important 🥺🥺🥺
Birthdays are important!! From your friends and some of your favorite players across MLB, happy birthday, @SlangsOnSports!
May is #ALSAwarenessMonth. Grab a book. Meet a friend. Pour some wine. Share their words. Learn how so many are fighting to #ENDALS. #thursdaymorning #BlitzYourLife 📕
May is ALS awareness month. Admittedly, 6 years ago I read “possible diagnosis: amyotrophic lateral sclerosis” I had little comprehension on the disease. I promised myself I’d share my journey with the world in hopes of bringing much needed awareness to ALS. Not easy but worth it
Wearing blue for my brother Phil today!
The great Lou Gehrig took himself off the Yankees lineup on May 2, 1939. Several months later, he would give his infamous speech declaring himself the “luckiest man.” Today, I am joining @LiveLikeLou4 in wearing #blue4Lou Do it for the Iron Horse. livelikelou.org/als-families
@LiveLikeLou4 @Pirates @Dodgers We will be there. Thanks for all you do for ALS and families.
@KylanMorris1 @LiveLikeLou4 Oh Kylan, you’re truly an inspiration!! An amazing cause, and I know you sharing your experiences is helping so many others! So selfless, your beautiful mom is so proud!! And you look absolutely beautiful! Peace&love ☮️💖
I was honored to represent @LiveLikeLou4 at the Chapman Phi Delta Theta Sword & Shield Banquet by sharing my lived #ALS experience + the impact that LLL's Connect & Serve program has for ALS families like mine. Learn more about Connect & Serve via the link in the comments⚡️
I can’t wait for this conversation about Lou Gehrig with @HopOnACure and @iamalsorg. Sign up to join us via Zoom.
Breaking: this event will now feature special guest interviewer John Driskell Hopkins! Join us and @HopOnACure for this awesome book talk with Jonathan Eig and Hop about Eig's new book "Luckiest Man: The Life and Death of Lou Gehrig." #believeinacure💙 iamals.org/action/the-luc…
Could not be more excited for Thursday night at Fenway. 3 days away, grab your tickets in the link below!! #kALS mlb.com/redsox/tickets…
3️⃣ Days Out ❤️ The 2024 ALS Awareness Game at Fenway Park is this Thursday! All ticket proceeds will benefit the Peter Frates Family Foundation. 🎟️ bit.ly/2024ALSGameTIX #strikeoutALS
Yesterday I had some visitors from the Babson College @phidelt chapter. Lou Gherig was brother in Phi Delta Theta in his days at Columbia University. It was great to be in a fraternity atmosphere again even though I was in a different fraternity.
In honor of #VolunteerAppreciationMonth, we've partnered with @LiveLikeLou4 to add a new feature to our website! Phi Delta Theta members can now visit our Locate Map to connect with ALS families in their area. Learn more: phideltatheta.org/join/locate-ph…