Por: CBS News Tech July 13, 2023
New York City — Brian Jeansonne talks to the world about his journey with ALS through TikTok videos, which the 46-year-old makes with his family and caregivers. He began recording them when he was still able to speak on his own.I'm married for almost 18 years, have five kids, Jeansonne said in one such video. , Jeansonne has been able to keep his ability to speak through a process called voice preservation. Imagine having no way to... + full article
ABC News USA Health September 25, 2023
WASHINGTON -- The Food and Drug Administration meets this week to consider approval of an experimental treatment for Lou Gehrig’s disease, the culmination of a yearslong lobbying effort by patients with the fatal neurodegenerative disease.Those advocates still face one giant... + más
What is ALS? Experts explain symptoms to look out for, causes and treatments | CBS News
Experimental treatment pushed by ALS patients gets day before FDA, but agency unconvinced it works | WPLG Local 10
WPLG Local 10 USA Politics September 25, 2023
WASHINGTON – The Food and Drug Administration meets this week to consider approval of an experimental treatment for Lou Gehrig’s disease, the culmination of a by patients with the fatal neurodegenerative disease.Those advocates still face one giant hurdle: FDA regulators say... + más
Experimental treatment pushed by ALS patients gets day before FDA, but agency unconvinced it works | ABC News
CBS News USA Health August 08, 2023
Sandra Bullock's longtime partner at age 57 after privately battling ALS, or Amyotrophic Lateral Sclerosis, for three years, his family said. The news brought new attention to the disease and prompted questions about what the diagnosis means.ALS is a progressive... + más
NFL Playoff Scenarios | ABC News
Le Krewe du Roi celebrates the state at 58th annual Mardi Gras Ball | The Advocate
ABC7 USA World April 26, 2023
a new drug Tuesday to treat a rare form of amyotrophic lateral sclerosis, or ALS.The drug Qalsody (tofersen) is expected to help people with a very specific mutation, SOD1, which applies to only 2% of the ALS population.In a statement, the FDA said it estimates there are fewer... + más
FDA gives OK to new drug to treat rare form of ALS | ABC7
FDA approves new drug for rare form of ALS | ABC News
ABC News USA Health April 25, 2023
The U.S. Food and Drug Administration a new drug Tuesday to treat a rare form of amyotrophic lateral sclerosis, or ALS.The drug Qalsody (tofersen) is expected to help people with a very specific mutation, SOD1, which applies to only 2% of the ALS population.In a statement, the... + más
WPTV USA Nation October 04, 2022
Imagine being trapped in a paralyzed body. That's how the describes the progression of a neurological disease called ALS, which 31,000 people in the United States are living with.Thankfully, there is hope for a better quality of life thanks to a drug that the Food and Drug... + más
FDA approves ALS drug partly funded by Ice Bucket Challenge | 10 WBNS
Highly debated Amylyx Pharmaceuticals ALS drug wins FDA approval | New York Post
About iurex | Privacy Policy | Disclaimer |