Get the scoop: https://bit.ly/3VJPmmI
Measuring levels in tear samples of a family of proteins linked to neuroinflammation may help in diagnosing ALS, a new study reports.

Get the scoop: https://bit.ly/3VJPmmI
Measuring levels in tear samples of a family of proteins linked to neuroinflammation may help in diagnosing ALS, a new study reports.
You deserve moments of ease wherever they can be found. Wishing you some gentleness today.
#ALS
Explore the details: https://bit.ly/4yLHQpS
As a caregiver, columnist Kristin Neva says she often feels powerless to change things, which is why she'll gladly take even small wins.
It’s understandable if your thoughts move in directions you didn’t expect.
#ALS
Kiersten, who lives with FA, shares a reminder about continuing to embrace life while navigating the challenges of disability.
Our ALS News Forums offer a space to connect, share experiences, and find community: https://bit.ly/47evHhh
Discover more: https://bit.ly/4im3Bqq
Ahead of MDA Engage: Dallas, keynote speaker Lily Sander discusses belonging, resilience, and the power of community and connection.
BARI’s Daniel Mordes and Julie Smeyers unpack how low TBK1 raises risk for ALS and related dementias. Cells can’t clear junk as well, and the brain’s immune cells get out of balance. Helpful look at a dual problem.
#ALS #dementia
www.frontiersin.org/journals/neu...
Your way of navigating today doesn’t have to look like anyone else’s.
#ALS
Discover more: https://bit.ly/4dzLf2K
Specialized care was linked to longer survival in people with ALS, with the strongest benefit seen in those with limb-onset disease.
When Riya Jain’s grandmother lost her ability to speak due to ALS, the communication tools available to her didn’t sound like her own voice: https://bit.ly/4zxKpvP
“Embrace technology and assistive devices as a means to maintain your independence.” 💙
Meet Michael, Bridging Voice Ambassador. He founded alsresources.org and is a Peer Support Specialist with I AM ALS. Office hours: Tuesdays 4:30pm ET, bridgingvoice.org/office-hours
🧠 Mapping the prodromal phase of sporadic ALS. Amyotrophic lateral sclerosis (#ALS) is diagnosed once motor impairment becomes apparent, but evidence suggests a subtle preclinical phase.
🔗Read a summary on our website: www.synergy-munich.de/news-events/...
Artificial intelligence may offer a new way to identify genetic risk factors.
Read more about the research and its potential implications for ALS genetic testing: https://bit.ly/4zBbE8V
#ALS #ALSResearch #AmyotrophicLateralSclerosis #Genetics #ALSNewsToday #Bionews
Get the scoop: https://bit.ly/3TT7Qk6
An AI model can distinguish people with ALS from unaffected individuals, with a high predictive performance, according to a study.
NeuroSense Moves Forward with Nasdaq Hearing as PrimeC Reaches Crucial Milestones #United_States #Cambridge #ALS #NeuroSense #PrimeC
🧊🚒 COLD WATER. STRONG BROTHERHOOD!
Your Calgary firefighters answered Chestermere's ALS Ice Bucket Challenge in support of firefighter Kimball Yorston! 💙
Now we're calling out Chris Chyka (Cochrane), Travis Wray (Okotoks) and IAFF 6th District VP Mike Carter!
You're up! 🥶🪣
Suma Babu, MBBS, MPH, and James Berry, MD, MPH, both past recipients of Next Generation Research Grants (in 2019 and 2013) are leading a #ClinicalTrial of the drug #foralumab to treat #ALS. The first three participants have received their first dose.
This Halloween season, we’re creating space for our community to share experiences and connect with others who understand.
We’re introducing “Scary Things We Face Anyway.”
Everyone is welcome to participate at their own comfort level: https://bit.ly/4dCY8Jj
Get the scoop: https://bit.ly/47b50Kj
Electrical stimulation of the spinal cord can reduce the buildup of toxic TDP-43 protein clumps in a mouse model of ALS, per a study.
"ALS is challenging: physically, emotionally, and financially. You cannot do this alone. Start preparing for the changes ALS can bring, and join ALS organizations and support groups." 💙
Meet Bruce & Susan, Bridging Voice Ambassadors.