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ALS affects an estimated 7.7 out of every 100,000 people in the U.S., according to the Muscular Dystrophy Association, which says between 15,000 and 20,000 Americans currently live with the ...
ALS is a neurological disorder that affects nerve cells in the brain and spinal cord that control voluntary muscle movement and breathing. As the nerve cells -- called motor neurons -- degenerate ...
A man with amyotrophic lateral sclerosis (ALS) who had lost his ability to speak has been able to communicate with a Blackrock Neurotech text-to-speech brain implant, researchers said in one of ...
AAC is used by those with a wide range of speech and language impairments, including congenital impairments such as cerebral palsy, intellectual impairment and autism, and acquired conditions such as amyotrophic lateral sclerosis and Parkinson's disease. AAC can be a permanent addition to a person's communication or a temporary aid.
The institute has raised and spent more than $100 million on research into effective treatments for ALS and practices open-source science. [19] After the discovery that the multiple sclerosis drug Gilenya might also be a treatment for ALS, the Institute enrolled 30 people in a Phase 2A clinical trial the drug in 2013, though it did not progress further.
Non-invasive ventilation (NIV) is the primary treatment for respiratory failure in ALS [10] and was the first treatment shown to improve both survival and quality of life. [5] NIV uses a face or nasal mask connected to a ventilator that provides intermittent positive pressure to support breathing.
The ALS Association is an American nonprofit organization that funds global amyotrophic lateral sclerosis (ALS) research, provides care services and programs to people affected by ALS through its nationwide network of clinical care centers, and works with ALS advocates around the country for state and federal policies that serve people living with amyotrophic lateral sclerosis (ALS), also ...
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