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Finding meaning together in life after 16 years with ALS. My husband, Todd, and I celebrated our 23rd wedding anniversary this week. We’ve spent 16 of those years with ALS since Todd’s diagnosis in 2010.
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Finding meaning together in life after 16 years with ALS
My husband, Todd, and I celebrated our 23rd wedding anniversary this week. We've spent 16 of those years with ALS since Todd's diagnosis in 2010. I've been thinking recently about how we have found meaning within this difficult life we've been living for
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ALS Nexus 2026: Speaker shares hope navigating mom's ALS
For Emmy award-winning host and New York Times bestselling author Tabitha Brown, joy, gratitude, and hope have guided her through life since losing her mother to amyotrophic lateral sclerosis (ALS) in 2007. Speaking this week at the ALS Nexus conference i
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ALS Nexus 2026: Implantable device decodes patients' brain signals
An experimental implantable device from Precision Neuroscience enabled computers to decode brain signals to predict movement and speech, which could eventually help create assistive devices for people with amyotrophic lateral sclerosis (ALS). That's accor
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ALS Nexus 2026: People with diabetes may have lower ALS risk, study says
People with diabetes may be less likely to develop amyotrophic lateral sclerosis (ALS) than those without diabetes, according to findings detailed in a poster presented at the ALS Nexus conference. The study also found that people with a longer reported d
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$1 million grant supports trial of experimental treatment for ALS
The ALS Association has awarded Mitochon Pharmaceuticals a $1 million grant to support a Phase 2 clinical trial testing the company's experimental therapy MP-101 in people with amyotrophic lateral sclerosis (ALS). The study is still in the planning stages
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