I Live With Lou Gehrig’s Disease—Here’s What I Want You to Know
Tell your healthcare provider right away or go to the nearest emergency room if you have any of the following symptoms: hives; swelling of the lips, tongue, or face; fainting; breathing problems; ...
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How you can help ‘Sharon’s Songbirds’ as we ‘Walk to Defeat ALS’
Several years ago our WJXT family was personally touched by ALS, also known as Lou Gehrig’s disease, when our beloved ...
This Startup Lets Paralyzed People Use Computers–Without A Chip In Their Head
Startup Cognixion, which has developed a noninvasive brain-computer interface, has begun a clinical trial for patients with ...
NeuroSense’s ALS drug PrimeC shows success in phase 2b, eyes final trial
PrimeC has been given an ‘Orphan Drug’ status by the FDA (Food and Drug Administration) and EMA (European Medicines Agency).
Progress spurred by ALS Ice Bucket Challenge — and what remains to be done 10 years later
The brainchild of two ALS sufferers, the Ice Bucket Challenge took off in August 2014 — and the initiative is still having an impact on the disease.
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Love Like Lou gala raises over $5,400 for ALS research
Emporia State fraternity Phi Delta Theta hosted the Love Like Lou Gala at the Bowyer Building to raise funds for ALS research. The fraternity has hosted the ...
ALS drug failures and why COYA 302 is different
ALS, which is also known as Lou Gehrig's Disease, is a rare neurological disease that affects motor neurons — the nerve cells ...
Inaugural Phi Delta Theta fundraiser nets nearly $10,000
Assembled by Arkansas Beta chapter of Phi Delta Theta, the event brought together 175 participants and raised close to ...
Registration underway to support Walk to Defeat ALS Sarasota at Payne Park
Sarasota-Manatee partnership offers free hearing support; job fairs in Bradenton, Sarasota; Goodwill opens LWR outlet; arts ...