Les Turner ALS Foundation
The leader in comprehensive #ALS care in Chicagoland
@longitudeprize.bsky.social
The Longitude Prize on ALS is a global initiative to incentivise the use of AI to transform drug discovery for the treatment of ALS (also known as MND or motor neuron disease), launching in 2025.
@adelboudi.bsky.social
Neuroscientist @ MassGeneral Hospital/Harvard Medical School Amyotrophic Lateral Sclerosis | Huntington's Disease
@jackie-derose.bsky.social
Neuroscientist turned strategic Marketer, driven by a passion for communicating pioneering brain discoveries.🧠 Also a foodie, wine, and travel lover, always seeking new and diverse experiences.🍷All posts reflect my own views.
@burningiceberg.bsky.social
Blue to the berry🫐 #BoycottOligarchs #MetaExit, #HopeForTruth Humanity is literally 🔥 on the line. #Holdtheline Fighting for a 🧬 cure for familial #ALS in honor of my family living with #FALS. #Remembering dad & grandma #FundNIH 5calls.org
@bridgingvoice.bsky.social
Non-profit supporting ALS clients with communication technology. Learn more at www.bridgingvoice.org.
@alsadvocacy.bsky.social
ALS = Lou Gehrig's Disease Thought it had been cured by now? Still no known cause. Still no cure. Still meh treatments. Still quickly fatal. Still outrageous. https://x.com/alsadvocacy
@alsassociation.bsky.social
Fighting ALS on every front through research, care services, and advocacy.
@jeanc9orf72.bsky.social
Genetic ALS & FTD Advocate, C9orf72 Carrier , Executive Director Genetic ALS & FTD : End the Legacy - East Bay California
@euanscentre.bsky.social
We conduct vital research into motor neuron disease. Based at the University of Eidnburgh, we unite over 250 scientists and doctors across Scotland.
@endpts.com
We're where the business of medicine gets answers. An independent news media organization covering biotech, pharma, science, policy, finance, venture capital and markets, and how they drive the life sciences industry. Read us at www.endpts.com.
@alsunitedct.bsky.social
ALS United Connecticut provides comprehensive support to improve the quality of life for people with ALS and their families while advocating for increased support and advancing innovative research for new treatments and an end to ALS.
@gordonjewett.bsky.social
Assistant professor at the University of Calgary | Neuromuscular Neurologist | ALS, neuromuscular, and digital biomarker researcher | Silly dad, bike & ski obsessed ⛰
@usha.bsky.social
I cover health equity for STAT. Yes my job is harder these days. Signal ID: usha.22
@andreaalsstrategy.bsky.social
ALS strategist| former caregiver| ex-CEO and board member| aligning interests of the lived experience ALS/MND community with research, clinical care, regulators, funders, and industry.
@butchart-doug.bsky.social
@lyleostrow.bsky.social
Neurologist/Neuroscientist at Lewis Katz School of Medicine, Temple University, and the ALS Hope Foundation. Director, TUHS ALS Postmortem Core collab with CDC ALS Registry. Chair, DoD (CDMRP) ALS Research Programmatic Panel. Views my OWN.
@jcny79.bsky.social
Just a girl diagnosed with ALS 3/30/22. Living life day by day while I continue to adapt and process this journey I was given
@lisalegacy4als.bsky.social
Lisa Stockman Mauriello fought for Expanded Access to an ALS treatment. Lisa passed away 8.4.21. Honorinf Lisa’s legacy by advocating for ALS.
@lccrow.bsky.social
ALS warrior since 2016. Trusting God and His plan. Santa Monica, California native, Georgia transplant. Daughter, sister, wife and mother
@carolinepurslow.bsky.social
Head of Health, Challenge Works (Nesta) - designing global innovation competitions, delivering the Longitude Prize #ALS #MND #Dementia #AMR.
@alswarriors.bsky.social
Widow due to ALS. Warrior because of ALS. Three words for ALS... WE WILL WIN! Dog momma. Musical Lover. Total Ham! my thoughts are mine and not my employer.
@michaelwheelson.bsky.social
Mechanical Engineer. Star Wars better than Star Trek. Agnostic Atheist. Oklahoma Blue Dot. ALS'ing since Feb. 2017.
@susancr.bsky.social
Vegan🌻 | Liberal Democrat | Social Justice | Climate Crisis | Animal Rights | Hoping for a Cure for ALS | Eagles. Flyers. Phillies | Have a Cat named Kat #EndALS #FundNIH #ALSAwareness #FuckTrump #BlueResisters #BlueCrew
@bertylee.bsky.social
MND researcher | educator | cyclist | drip-coffee enthusiast | husband and father. Posts express my views
@constancemm.bsky.social
ALS Advocate - SOD1 - Chicago Cubs fan - St. Paddy’s is the only holiday ☘️
@real-anatomic.bsky.social
Stem cell focused research with applications in pain, ALS, CMT, and cancer drug discovery. Recreating in vitro models one cell type at a time.
@dlwchico.bsky.social
random old dude on the internet. I like critters. He/Him. spoon9930 on discord. I'm in Norcal. 20+ year colorectal cancer survivor. New to the wheelchair life. "Fuck every cause that ends in murder and children crying" — Iain Banks Turns out I have ALS.
@citronbokbinderi.bsky.social
PLS/MND warrior 💪👩🦽➡️ Book bindery; Citron Bokbinderi Njutånger 💛🍋📚 Photographer; fotograf anna-lisa 📸💚 Living in northern Sweden 🇸🇪 www.citronbokbinderi.com #PLS #MND #ChronicIllness #Bookbinding #Photography
@mitogc.bsky.social
Smithie 2014, mitochondrial disease, spoonie, rare disease, genetic counselor, 🏳️🌈 ♿️ opinions are my own
@alstdi.bsky.social
The most comprehensive lab focused on ALS/Lou Gehrig's Disease. We are the Drug Discovery Engine discovering & inventing effective treatments for ALS. #EndALS www.als.net
@webblauren.bsky.social
@buffer.com
Create and share social media content anywhere, consistently. Built with 💙 by a global, remote team. ⬇️ Learn more about Buffer & Bluesky https://buffer.com/bluesky
@bsw5020.bsky.social
Dad, husband, activist, entrepreneur, unlikely movie star, living with ALS, a currently fatal disease. www.iamals.org/als-awareness-month #ALSisHere #SoAreWe
@bsky.app
official Bluesky account (check username👆) Bugs, feature requests, feedback: [email protected]