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Brooke Eby shares her Lou Gehrig’s disease, or ALS, diagnosis at age 33 and details her outlook on life after getting a terminal prognosis in her 30s. I thought I was too young to have ALS. Then ...
Amyotrophic lateral sclerosis (ALS), also known as motor neuron disease (MND) or (in the United States) Lou Gehrig's disease (LGD), is a rare, terminal neurodegenerative disorder that results in the progressive loss of both upper and lower motor neurons that normally control voluntary muscle contraction. [3]
Symptoms of motor neuron diseases can be first seen at birth or can come on slowly later in life. Most of these diseases worsen over time; while some, such as ALS, shorten one's life expectancy, others do not. [2] Currently, there are no approved treatments for the majority of motor neuron disorders, and care is mostly symptomatic. [2]
At age 63, Mark’s diagnosis was official: He had ALS, a disease with which most people are only expected to live three to five years after symptoms develop. “It was a hard pill to swallow ...
Researchers identified a new biomarker for predicting the clinical outcome of patients with ALS, Amyotrophic Lateral Sclerosis, through brain imaging. Researchers Say This Test Can Predict ALS ...
Symptoms may include difficulty with balance, weakness and stiffness in the legs, and clumsiness. Other common symptoms are spasticity (involuntary muscle contraction due to the stretching of muscle, which depends on the velocity of the stretch) in the hands, feet, or legs, foot dragging , and speech and swallowing problems due to involvement ...
Excitotoxicity may be involved in cancers, spinal cord injury, stroke, traumatic brain injury, hearing loss (through noise overexposure or ototoxicity), and in neurodegenerative diseases of the central nervous system such as multiple sclerosis, Alzheimer's disease, amyotrophic lateral sclerosis (ALS), Parkinson's disease, alcoholism, alcohol ...
The patient's older brother, father, and paternal uncle had previously all died of ALS or an ALS type syndrome. The patient developed progressive bulbar palsy, became dependent on a respirator, and had two episodes of cardiac arrest. The patient died from pneumonia two years after the onset of the disease.