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At work, I was usually the one making jokes and people would tell me to be more serious. But I think it was instilled in me for a reason. When I was diagnosed with ALS, I took some time to be sad.
Amyotrophic lateral sclerosis (ALS), also known as motor neurone 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]
Lee Wilson discovered she has a "100%" chance of developing ALS, after losing her father and grandmother to the disease
ALS can manifest in people differently, but it usually starts with weakness that spreads or gets worse over time, according to the Mayo Clinic. Here are some of the symptoms of this fatal disease.
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]
Wallach was diagnosed with ALS in 2017 at the age of 37 on the same day he and his wife brought home their second daughter from the hospital. [3] Originally visiting the doctor for a persistent cough, Wallach had also mentioned experiencing muscle tremors and weakness in his left hand and was told he probably had a progressive neurodegenerative disease. [2]
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that typically affects adults around 54–67 [1] years of age, although anyone can be diagnosed with the disease. People diagnosed with ALS live on average 2–4 years after diagnosis due to the quick progression of the disease.
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