Live Like Lou
@livelikelou4
Leaving ALS better than we found it #ONWARD #LiveLikeLou
ID: 1283436080
https://livelikelou.org/ 20-03-2013 14:38:34
1,1K Tweet
883 Followers
477 Following
Goo Goo Dolls
@googoodolls
SUMMER ANTHEM TOUR 2025 US & AU dates on sale now at googoodolls.com/tour
HOMAGE
@homage
Pay homage. | Vintage-inspired apparel. Order Questions? E-mail an All-Star: [email protected]
ALS Advocacy
@alsadvocacy
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.
Neuroscience News
@neurosciencenew
Official Neuroscience News Twitter. Brain research news articles on neuroscience, psychology, AI, neurology, brain cancer, robotics, mental health & science.
Society for Neuroscience (SfN)
@sfntweets
The largest nonprofit of scientists & physicians devoted to understanding the #brain & #nervoussystem. Follow us at @NeuronlineSfN, @SfN_Events & @SfNJournals
Manolis Kellis
@manoliskellis
Dissecting disease mechanism. Single-cell, Epigenomics, Regulatory Genomics, Disease Genetics, Brain, Cancer, Metabolism. @MIT Prof, @MIT_CSAIL, @BroadInstitute
ALS Uncensored 🏴☠️
@scottsfight
Scott Craig. ALS Uncensored podcast. Digital Artist. AI Student. Typing with my eyes. Living Impossible! #ALSUncensored #ALS #EyeGazeArtist #AI #IWriteALS
Danica S
@symi2
ALS Advocate #EndALS #WorldWithoutALS
Jan Mattingly
@mattwoman
✡️ Canadian, ALS hater, will like or RT any authentic ALS tweet. I know great loss: My loving son passed from ALS June 2022.
Team Hilliard Foundation
@teamhilliardals
Team Hilliard Foundation, a 501C-3 Charity to fund research for a cure for ALS and support families facing ALS. Phil 4:6 teamhilliardfoundation.org
NIH Director
@nihdirector
Official account of the @NIH Director Posts prior to 01/21/2025 were from former NIH Directors Engagement ≠ endorsement Privacy: go.usa.gov/x9svN
Willy
@willygrant
Digital Maven. Corgi mom, BBQ, art & books. Punk. KCBS Judge. Single. Born in #YVR. Lives in #YEG #GoodTwitter 🇨🇦
Sandra Abrevaya
@sabrevaya
Wife to @bsw5020. Mama. Caregiver. CEO @synapticure providing medical care for Alzheimer’s, Parkinson’s and ALS. Co-founder @iamalsorg. EP @noc_film.
The Lou Gehrig Experience
@louishgehrig4
I'm not a headline guy...
Nidhi Sharma
@sharma_90
Postdoc @university of Chicago working with @krasiosL where I am exploring neurodegenerative (Alzheimer’s and ALS).Science lover and travel addicted .
Steve Gleason - "Live Impossible"
@stevegleason
New Instagram - @stevegleasonofficial Dad. Husband. Inspiring all people to live purposefully, despite tragedy. I tweet with my eyes. Embracing ALS.
Christian Yelich
@christianyelich
Instagram: ChristianYelich
Chris Myers 💻🧬🧪☕ ℏ⁻³/N!∬exp(-βĤ) d𝓅 d𝓺
@bayouphysicist
Professor Physics/Chemical Biophysics💻🧬☕ 🌇 @fordhamnyc 🎓: @riceuniversity🦉 @bcmhouston Formerly: @NYUniversity ⋒ @UmBiophys〽@UTMBhealth
Girl Travelin Alone
@cathystandish
Nancy Beyke
@nancybeyke
Wife, Mom and Mama currently living with ALS.
Seth Poling
@sethpoling10
Wild & Wonderful WV. FSU grad. Married to @erika_poling , Father to Liam & Bayler, ALS Warrior & advocate. #EndALS Founder of @project_seth
MND Association
@mndassoc
Our vision is a 🌎 free from 𝐦𝐨𝐭𝐨𝐫 𝐧𝐞𝐮𝐫𝐨𝐧𝐞 𝐝𝐢𝐬𝐞𝐚𝐬𝐞 #MND
Clare Durrett 🏳️🌈
@claredurrett
Working on making my life worthwhile one day at a time. Tweets are my own. All in for Team Gleason and Answer ALS.
Mayuri Om Saxena
@mayuri_saxena
40yo living with ALS on Life support. Author. Creative Director. Advocate. Dreamer. Public Servant. ALSFRS 1/48 linktr.ee/mayurisaxena
Leanne Yacyshyn
@leanne_yacyshyn
Wife. Mom of 2 teens. Former elementary school teacher. Canucks fan. Living with ALS and waiting for the day it is no longer terminal.
Phil Rosenthal
@philrosenthal
Somebody Feed Phil Season 7 Streaming NOW on @Netflix | JUST TRY IT! Kids Book w/ Lily Rosenthal | Season 8 is coming!
Fernando G Vieira
@fgvoneforty
Dad. CEO & CSO at ALS TDI. Talk less, work more. Opinions expressed on this account are my own.
Numotion
@gonumotion
We customize power and manual wheelchairs, scooters, seating systems, adaptive equipment and more for people of all ages. #MissionPossible
Kylan Morris
@kylanmorris1
ALS Patient Advocacy | @sandymorris333🌻
Jamie Smith
@jamielw8
Mother I Widow I Pediatric Respiratory Therapist Fighting for reform in health care and research for ALS.
Mitchell Bat Co.™
@mitchellbatco
Officially Licensed by Major League Baseball PA, Colleges & NIL. Heritage-Inspired Baseball bats hand-painted in Nashville, TN since 2013. 👀@espn
Longitude Prize on ALS
@longitude_prize
The Longitude Prize series from innovation prize experts @Challenge_Works. Longitude Prize on ALS launching June 25th 2025!
CVV, PhD
@cvandevelde75
Professor, ALS Researcher, #womeninSTEM, boy mom, and gin drinker. Working for the cause, not the applause. ECM.
Angela Kocot
@gailaonearth
mom of 3, geographer, community volunteer, humanist. #ALS widow
Hunter Greene
@huntergreene17
Cincinnati Reds//////Instagram : @therealhuntergreene
Fergal Waldron
@fergalwaldron
Advanced Research Fellow @aberdeenuni | MND/ALS & neurodegenerative diseases | Clinical heterogeneity | Immunity & neuroinflammation | Genetics | Data synthesis
Jack Humphrey
@jackhumphrey_
Trying to understand neurological disease through genomics. Out-reacher. Occasional boulderer. Instructor at Mount Sinai.
Yale Pathology
@yalepathology
We are internationally recognized experts in molecular & anatomic pathology, contributing to Yale's leadership in scientific research, teaching & patient care.
BaseballHistoryNut
@nut_history
Baseball History Nut *I do not claim to own any of these images* 🇨🇦. Slowly building a card collection. Contact: [email protected]
ALS TX DAD
@alsdads
I AM ALS
@iamalsorg
I AM ALS is a patient-led movement revolutionizing how to end disease with our sights set squarely on ALS.
Lilian || 采葳
@liliantwlin
Sarah Nauser
@sarahnauser
Dominating ALS one day at a time since 2018. Retired Police Officer. “Love the life you live and live the life you love” Go Royals! 💙#FightLikeAGirl
Donnelly Lab
@donnelly_lab
The Donnelly Lab and LiveLikeLou Center for ALS Research at the University of Pittsburgh. We study the molecular causes of neurodegenerative disease.
Wilfried Rossoll
@rossolllab
translational Neuroproteomics Lab | We study protein (dis)aggregation in ALS/FTD, AD, and other neurodegenerative proteinopathies. (Views are my own.)
Nashville Stars ⚾️
@nashvillestars
Deeply rooted in Tennessee’s rich baseball history, we are committed to bringing Major League Baseball to Music City in partnership with the @NLBMuseumKC
Eikonizo Therapeutics
@eikonizo
Envisioning an end to neurodegenerative and other diseases
David Gate
@dgatelab
Director, Abrams Research Center, Northwestern Neurology. The Gate lab studies the immune system in neurodegenerative diseases.
Chen Eitan
@chen_cep_eitan
Postdoctoral Fellow @NIH_NINDS | ALS researcher | focusing on neurogenetics in neurodegenerative diseases
AZ Latina ☮️🌊🟦
@avoice4als
Advocate for Amyloidosis, ALS & Rare Diseases. Enviro Justice, Foster Care & Gun Safety. Love LA sports. @EndRareDiseases on bsky
Kathy Collier
@kathyco74123384
ALS Advocate. Proud Mom of an Autistic Son. NEVER Forget Richard my ALS ANGEL.
Tom Fitz 👨🏻💻💡🔌
@_wobblewobble
I’m just a guy fighting ALS the best I can, tweeting about all things programming 👨💻and my toddler 👼
Björn Vahsen
@bvahsen
Postdoc in Talbot Lab @MNDOxford @NDCNOxford @KavliOxford and Junior Research Fellow @KelloggOx, using stem cell models to research microglia in ALS/MND.
Barmada Lab
@barmadalab
Barmada lab @UMich. We study cellular mechanisms underlying ALS/FTD & RNA biology with focus on neurodegeneration. (group-run account)
Patricia Manhardt
@patriciamanhar1
Begging for the lives of people with ALS. Praying that those who should be fighting with this community will join us. #NurOwnWorks
Tolt Technologies LLC
@tolt_tech
Lisa's Legacy for ALS
@lisalegacy4als
Lisa Stockman Mauriello fought for Expanded Access to an ALS treatment. Lisa passed away 8.4.21. Honor Lisa’s legacy by advocating for ALS.
juan
@juan23188549
Hard working, helpful, honest,
GregoryLab
@gregorylab7
Our lab are interested in understanding the non-motor manifestations of motor neuron disease including cognition and the gut-brain axis.
Brooke Eby
@limpbroozkit
just a gal with ALS
Neuromuscular Study Group
@nmsg_news
Follow us for Neuromuscular Study Group updates, including news of the NMSG24 conference. We welcome researchers working across pre-clinical & clinical study
Rothstein Lab
@rothstein_lab
Dr. Jeffrey Rothstein is a professor of neurology and neuroscience @HopkinsMedicine and is the founding director of @packardcenter. (trainee run)
The LEITH Lab
@leithlab
LEITH Lab strives for compassionate care and humanizing research in rare diseases among historically underrepresented communities. Directed by @AudreTaughtMe2
Tee to Green
@bluefairways7
Golfer-Cannabis-MJ/MMJ advocate. Making better medicine.
Sandra W. Marlowe
@sandrawmarlowe
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.
Mitsubishi Tanabe Pharma America
@mtpa_us
MTPA is dedicated to making a real difference in the lives of people living with serious and debilitating diseases. Community guidelines: bit.ly/4e9gM93
Mandi
@runningmama0522
Brian Wallach
@bsw5020
Dad, husband, activist, entrepreneur, unlikely movie star, living with ALS, a currently fatal disease.
End ALS Now
@endalsnow
▪Bri ▪I mainly amplify #ALS tweets ▪ALS=wretched, cruel, 100% fatal ▪RT=awareness, not agreement ▪🚫DMs🚫 ▪#EndALS ▪#SunflowerForSandy 🌻 ▪#RoseForJamie 🌹
Prof Jenna Gregory
@jennagregory488
Pathologist and ALS/MND researcher