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Rebecca Gayheart Dane on caring for her late husband, Eric Dane, and synthetic voices The wife of 'Grey's Anatomy' actor Eric Dane says caring for him gave her an "extra dose" of compassion for others.

Rebecca Gayheart spoke with NPR about caring for her late husband Eric Dane during his battle with #ALS

She shared the emotional experience of watching him lose his voice—and how new voice technology helped preserve it.

www.npr.org/2026/03/11/n...
#Caregiving #DisabilityAwareness

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Finding your own rhythm: https://bit.ly/3KWD7gV

Dagmar Munn reflects on how actions, like balloon-blowing, humming, or mindful breathing, can help maintain a sense of control while living with ALS.

#ALS #ALSNewsToday #Bionews #AmyotrophicLateralSclerosis #ALSCommunity #LungHealth

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The way you handle today is enough, whatever that looks like.

#ALS

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You’re allowed to acknowledge what today looks like without downplaying it.

#ALS

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Your experience is part of a wider story that deserves recognition.

#ALS

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Months Before His Death, Eric Dane’s Estranged Wife Detailed How His Healthcare Insurance Kept Denying His Treatment “The woman from his insurance said to me, ‘You can keep applying, and I’ll keep denying.’ I was like, ‘Oh? F that.’”

Americans of all backgrounds and income statuses are victim to delays and denials imposed by health insurance giants. Months before his death, actor Eric Dane was approved for his #ALS treatment after going through two appeal processes.

Read more via @BuzzFeed >> buff.ly/illiXkl

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Three people, one in a wheelchair, conversing; join ALS News Today’s private ALS Conversations support forum.

Three people, one in a wheelchair, conversing; join ALS News Today’s private ALS Conversations support forum.

Looking for a space? https://bit.ly/4s9Ic6B

We’ve created a new private group inside the ALS News Today forums just for forum members.

#ALS #LivingWithALS #ALSCommunity #ALSNewsToday #Bionews

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Baseball Is The Best T-Shirt Baseball is the best, and we’re proud to partner with PitchingNinja in support of Sarah Langs. Proceeds from each shirt sold will benefit Project ALS and help in their mission to end ALS. Premium t-sh...

In honor of the day, and in anticipation of Opening Day, I’m wearing my @slangsonsports.bsky.social “Baseball is the Best” #ALS fundraising T-shirt.

Link: rotowear.com/products/bas...

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Support is available: https://bit.ly/3MOay6Q

Emotional distress can become overwhelming, but help exists through professionals, support networks, and crisis resources when needed.

#ALS #MentalHealthSupport #CaregiverSupport #ALSSupport #RareDisease #PatientSupport #Bionews #ALSNewsToday

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Vanavond, nou eigenlijk vannacht, ga ik lopen om geld in te zamelen voor onderzoek naar #ALS.

Iedereen die een donatie gedaan heeft, ontzettend bedankt! En mocht je nog twijfelen om dat te doen, het kan nog steeds!

www.alssunrisewalk.nl/fundraisers/...

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American Red Cross Wsi CertificATIon Exam TEST BANK Latest 2024 2025 Questions Answers For Water Safety Instructors
#testbank #testbankforAmericanRedCross #Wsi #Wsi2026 #AdvancedLifeSupport #ALS #ALS2026 #nursing #hackedexams

www.hackedexams.com

www.hackedexams.com/item/120080/...

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RT1999 will be tested in a UK ALS platform trial using NfL blood biomarker; early lab data show neuron protection.

RT1999 will be tested in a UK ALS platform trial using NfL blood biomarker; early lab data show neuron protection.

New ALS trial underway: https://bit.ly/4rrupqw

Researchers are preparing to test a new experimental therapy called RT1999 in a ALS platform trial designed to screen potential treatments more quickly.

#ALS #ClinicalTrials #ALSAwareness #ALSNewsToday #Bionews

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Your worth isn’t measured in tasks, energy, or output.

#ALS

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Understanding disease progression: https://bit.ly/4aGd7jp

ALS affects everyone differently, but learning about common stages can help with planning, expectations, and support decisions over time.

#ALS #ALSStages #ALSAwareness #LivingWithALS #CaregiverSupport #RareDisease #Bionews #ALSNewsToday

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Comprehensive Physiology | Review Spotlight 🔦 A look back at impactful work from the lab of Jun Sun 🔬 Last year, their team published in Comprehensive Physiology, advancing our understanding of #gut-brain barrier dysfunction in #ALS. Great science worth revisiting!
https://ow.ly/wGqs50Yqrfj

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I'm supporting ALS of Michigan! ALS of Michigan is a voluntary not-for-profit organization, solely dedicated to the fight against ALS. Our mission is dedicated to helping our pALS (people with ALS), their families and caregivers live life as fully as possible. We serve pALS and their families throughout the state of Michigan through a variety of programs. Thanks to our generous supporters, our programs are all offered at no cost ever.

🚴‍♂️ Mike & Thomas are cycling from Denver to the Grand Canyon to raise $34K for ALS of Michigan! Support grants for pALS: https://bit.ly/pedal4ALS

📅 ALS Night @ Jimmy John’s Field: June 26
📅 ALS Webinar w/ Dr. Shugars & John H.: Mar 26, 4‑5 PM
#ALS #ALSofMichigan #PedalForALS #CommunitySupport

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Earlier detection has the potential to change how ALS and other neurodegenerative diseases are diagnosed, studied, and ultimately treated.

vist.ly/4uj8j

#longevity #diagnostics #funding #ALS #biomarkers #earlydetection

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We're so proud to call Amy & Peggy Bridging Voice clients 💙 Amy founded @opals4als — a nonprofit bringing free beauty & wellness services to people living with ALS — after her own diagnosis. Read more: www.cbs58.com/news/natalie... #ALS #OPALS4ALS #BridgingVoice

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Tools can help: https://bit.ly/4qK08Dc

Assistive devices can support independence, comfort, and safety as needs change. Many families find that the right equipment makes daily life more manageable.

#ALS #AssistiveTechnology #CaregiverSupport #RareDisease #Bionews #ALSNewsToday

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Stay up-to-date with all of ALS United Rocky Mountain's News and Stories on our website at alsrockymountain.org. 

Read more on our website at https://alsrockymountain.org/who-we-are/news-stories/ and join us as we continue the fight to #EndALS.

#ALS #Advocacy #ALSUnited #TogetherWeEndALS®

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Pioneering Eye Test by Amydis Receives NIH Grant to Transform ALS Detection Amydis Inc. has secured a NIH Phase 2 grant aimed at advancing a groundbreaking eye test to detect a critical biomarker linked to neurodegenerative diseases like ALS.

Pioneering Eye Test by Amydis Receives NIH Grant to Transform ALS Detection #USA #San_Diego #ALS #Amydis #TDP-43

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An editorial from JAMA Neurology titled "Air Pollution and Motor Neuron Disease—Particulate-ly Risky" by Holly Elser, MD, PhD@1,2; Jill Goslinga, MD, MPH@3,4. Published online January 20, 2026. doi:10.1001/jamaneurol.2025.5378

An editorial from JAMA Neurology titled "Air Pollution and Motor Neuron Disease—Particulate-ly Risky" by Holly Elser, MD, PhD@1,2; Jill Goslinga, MD, MPH@3,4. Published online January 20, 2026. doi:10.1001/jamaneurol.2025.5378

Editorial: Robust evidence links chronic air pollution exposure to increased risk and accelerated progression of #ALS. ja.ma/4s7uGQO

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Meet Irati Mitxelena - CRISPR Technology for ALS Treatment
Meet Irati Mitxelena - CRISPR Technology for ALS Treatment YouTube video by CIC bioGUNE

#bioGUNE_EmpoweringWomen | 🚺 Meet Irati Mitxelena

This #WomenInBiosciences episode features her work on using #CRISPR to target #ALS mutations in #CICbioGUNE
@brtaeus.bsky.social, developing non-viral delivery systems and advancing gene-editing therapies

🎥 www.youtube.com/watch?v=lYWZ...

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Read this honest perspective: https://bit.ly/4o5Sd2d

In this new column, Iomar Barrett shares his experience and why having realistic expectations can help prepare patients and caregivers for the road ahead.

#ALS #ALSNewsToday #Bionews #ALSCommunity #ALSStories #ALSAdvocacy #ALSProgression

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Text asks how to deal with isolation and loneliness above a solitary man standing by a lake facing wooded hills.

Text asks how to deal with isolation and loneliness above a solitary man standing by a lake facing wooded hills.

Connect with others: https://bit.ly/4bneJij

#ALS #Coping #LifewithALS #ALSNewsToday #Bionews

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Female-specific Cx3cr1-driven regulation of #ALS and #Alzheimer’s risk genes in #tauopathy

Ari Sudwarts & Gopal Thinakaran @thinakaran.bsky.social #microglia #transcriptome

link.springer.com/article/10.1...

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The time is now to defeat ALS! For people battling ALS, time is not a luxury to waste. With an average life expectancy of 2-5 years following diagnosis, there is clear urgency to optimize care and find effective treatments for thos...

ALS takes away the ability to walk, dress, write, speak, swallow, and breathe. But, with every scientific advance, we get closer to the cure. Please support me with a donation to the Walk to Defeat ALS today! secure2.convio.net/alsa/site/TR... #ALS

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🏃 Run ALS Colfax runners! Join our Meet & Greet on April 29, 5–7 PM at Road Runner Sports in Westminster. Connect with runners, enjoy snacks, get shoe fittings, and 10% off purchases benefiting ALS United Rocky Mountain. RSVP by April 24: tami@alsrockymountain.org
#RunColfax #ALSUnited #ALS

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