Explore tweets tagged as #ALSAwareness
ALS is relentless. So are the patients and research teams fighting it. For the 30,000+ Americans living with amyotrophic lateral sclerosis, every day matters. New treatments are on the horizon!. 🎥 #ALS #ALSAwareness #FixInsurance #Biotech #Innovation
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In my recent episode of I'm Dying To Tell You Podcast, I chat with four remarkable women as they share how they found joy, community, and purpose after losing their loved ones to ALS. LISTEN LINKS:.or .@ALSTDI .#ALSawareness
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During the final week of #ALSAwareness Month, we’re spotlighting what matters most — the people we serve in our ALS community. 💙. This week, we’ll share powerful stories of resilience, joy, and connection made possible through communication. #ALSawareness #BridgingVoice
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June 21 is #GlobalMNDAwarenessDay. We spotlight the International Alliance of ALS/MND Associations for leading global advocacy. MND/ALS affects movement, speech & breathing but not the mind. Awareness drives action. #ALSAwareness #MNDCommunity #WorldPatientAlliance
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QurAlis thanks @Eikonizo for the #icebukcetchallenge nomination - challenge accepted! We are honored to participate to raise #ALSawareness as part of the 10th Anniversary of the ALS Ice Bucket Challenge. QurAlis' CEO and co-founder @RoetKasper and CTO Hagen Cramer got “soaked” on
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Dr Coco Newton reflects on this podcasts' 341st episode. In which, Debbie Lower (guest) opens up about how ALS and FTD have affected her and her family. Read in BioNews: #ALS #FTD #GeneticTesting #ALSAwareness #C9ORFGene #DNA #Dementia
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Answer ALS stands out with our unique, data-driven approach to ALS research, bringing together scientists, researchers, and those with lived experience, in a collaborative effort. Find out more at: #AnswerALS #ALSresearch #EndALS #ALSAwareness
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Anne Snyder says Emma from the @youralsnetwork was a light in the dark, guiding her family through ALS and VA support. Sometimes the right person changes everything. #MomentsThatMattered #ALSawareness #SupportIsStrength #BetterTogether #VeteransWithALS
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Please Share and give @MND777challenge a Follow 💙💙💙 #TeamMND #mnd #motorneuronediseaseawareness #mndwarrior #als #alsawareness #mndfeminabellator #googlemnd #mnda #mndawareness #twitching #mndefiance #MNDQUEENS#MelEvansMBE#MND777CHALLENGE.@clarkemartyn1 @MND777challenge
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I don’t post as much on here as IG, TT and FB but I still thank you for your support 🙏🏻♥️ #TeamMND #mnd #motorneuronediseaseawareness #mndwarrior #als #alsawareness #mndfeminabellator #googlemnd #mnda #mndawareness #twitching #fasciculations #mndefiance #MNDQUEENS#MelEvansMBE
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Both electronic and nonelectronic augmented alternative communication methods can help you connect with your loved ones meaningfully. Explore the options: . #ALS #AmyotrophicLateralSclerosis #ALSCommunity #ALSLife #LivingWithALS #ALSAwareness
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Mindy Uhrlaub’s powerful and inspiring memoir is a work of courageous transformation" —V (formerly Eve Ensler), author of The Vagina Monologues. Last Nerve is out now! #Sponsored #Memoir #MemoirReads #ALSAwareness #NonFictionReads #2025Reads
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Debunking myths about ALS helps bring to light the true personal impact of ALS and the critical importance of ongoing research. Read more at and share to raise awareness. #ALS #ALSAwareness #EndALS #LouGehrigsDisease #answerALS
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I read all 4 book pairings for the #fightalsfilmfest last month and while the topic of #ALS is extremely heavy, the awareness that comes from seeing #amyotrophiclateralsclerosis in mainstream media is invaluable . #alsawarenessmonth #ALSAwareness #HerALSStory #alstdi #sunnystrong
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Dr. Ximena Arcila Londono celebrated the 10th Anniversary of the ALS Ice Bucket Challenge, sponsored by the ALS Association Michigan Chapter! Dr Arcila is the Director of the Harry J. Hoenselaar ALS Clinic at Henry Ford Hospital. #ALSIceBucketChallenge #ALSAwareness
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ALS is amyotrophic lateral sclerosis. It’s a Neuro inflammatory disorder that impacts the brain as well as the final cord. There is no cure. #ALS #ALSAwareness #lougehrigsdisease #medical #Doctor #Disease #Neuroscience #Neurosurgery #Neurology
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86 years ago today, Lou Gehrig gave his "Luckiest Man" speech and brought international attention to #ALS. His legacy continues to raise #ALSAwareness and support in the search for a cure.
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Just a few of the experts answering your questions on Hear more in episode 107 of I’m Dying To Tell You Podcast. @iamalsorg @ALSTDI @HopOnACure @HopeLovesCo @limpbroozkit @loriandre3 #als #alsawareness #mnd
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