Over 16 years of living with ALS, Dagmar Munn says she has changed the way she responds when her body does not move the way she expects: https://bit.ly/4e39UN4

Over 16 years of living with ALS, Dagmar Munn says she has changed the way she responds when her body does not move the way she expects: https://bit.ly/4e39UN4
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A progressive decline in lung function is unavoidable in ALS, but there are steps that patients can take to improve breathing issues.
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Low muscle mass in the arms and legs and sarcopenia were linked to poorer survival in people with ALS in a small prospective study.
A targeted treatment for a rare genetic form of ALS has met its main goal in a Phase 3 trial.
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Columnist Kristin Neva takes note of the changing seasons with an initial sense of dread, then refocuses on the good things that also come.
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Phase 3 FUSION results suggest a targeted therapy may slow disease progression in FUS-ALS, with benefits seen versus placebo.
“While scrolling through social media the other day, I came across a question that stopped me in my tracks: How has having ALS impacted your life for the better?” -Dagmar Munn
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ALS disrupted her relationship with her body, so columnist Dagmar Munn developed small, intentional habits to restore her confidence.
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Mouse model study finds molecular changes in inflammation, RNA, and protein processing before ALS symptoms appear.
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ALS may change what marriage looks like for guest columnist Nancy Muirhead and her husband, but it cannot change their love.
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Researchers identified changes in 10 genes that may help diagnose or track ALS, according to a computer analysis of thousands of genes.
A woman with a progressive motor neuron disease was able to generate her own words in real time using an investigational brain-computer interface: https://bit.ly/475unNs
#ALS #ALSResearch #BrainComputerInterface #ALSNewsToday #Bionews
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The first healthy participant has been dosed in a Phase 1 clinical trial of ACE-2223, an experimental treatment for ALS.
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Geneuro received a European patent for GNK-301, an ALS therapy candidate targeting a viral protein thought to contribute to the disease.
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A brain-computer interface enabled a woman with a motor neuron disease to generate her own words in real time, according to its developer.
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Columnist Kristin Neva pauses to reflect on the uncertainty of living with ALS, even as she commits to making memories with her husband.
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Keynote speaker Mindy Henderson redefines "impossible" ahead of MDA Engage: Chicago, taking place Sept. 25-26 at the Westin Chicago Lombard.
When “How are you feeling?” is always a complicated question as a patient or caregiver. 😅
Living with ALS or caring for someone who is? Connect with others who get it: https://bit.ly/4rcO8vI
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A fitness routine columnist Dagmar Munn developed for a wellness project became a core part of her own exercise regimen after her diagnosis.
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The 100th participant has been enrolled in a Phase 2/3 clinical trial testing COYA 302, Coya Therapeutics’ experimental therapy for ALS.