Amyotrophic lateral sclerosis (ALS; also known as Lou Gehrig's disease in Canada and the United States, as motor neurone disease (MND) in Australia, Ireland, New Zealand, South Africa, and the United Kingdom, and Charcot disease in francophone countries) is a neurodegenerative neuromuscular disease that results in the progressive loss of motor neurons that control voluntary muscles.

In my late teens I began experiencing muscle twitching in lower extremities (calf muscles) by my mid twenties I happend to read an article on ALS and was horrified to learn I had symptoms of the disease, so i went to my family doctor and had blood work done, after that he refered me to a neurologist and and was tested using electromyography over the course of three months, the conductivity

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It's one of the biggest differences between als and Kennedys Disease. (Which also accounted to my +1 reflexes in both legs. ) I do not have ALS. THIS IS NOT A PLACE FOR UNDIAGNOSED INDIVIDUALS WITH BFS!!!! ALS IS A RARE DISEASE! I do knave facial (atrophy and weakness) ,and arm and leg weakness.

Today, that problem is gone—but the compan Reddit AMAs are "Ask me anything" forums where one user hosts the forum and others ask any question of the host.

This is what will happen eventually to all ALS patients if they don’t die from a non-ALS cause. What kills the ALS patient is the inability to take breaths. Mechanical ventilation can extend survival, but even that will eventually fail. According to one study, the extension averaged 14.9 months.

Healthy and active. Started having heavy night sweats and strong fasiculations (mostly on my back). Also noticed a balance problem when closing my eyes while in the shower.

6 dec. 2013 — Infektionen ger olika symptom beroende på vilka nervbanor som störs av bakterien. – En inflammation runt spinalnerverna kan kännas som 

And want to know what symptom or symptoms led to you getting tested. I'm sorry if this post is inappropriate but I also want to emphasize that I'm not self-diagnosing. Symptoms may begin for no reason and have no explanation other than stress and anxiety. You don't even have to feel stressed for it to begin. ALS weakness would mean clinical weakness (inability to do something) not the feeling of weakness, twitching occurs after clinical weakness has begun, usually starts in one area, never has good/bad days, and pain does not set in until later stages.

And want to know what symptom or symptoms led to you getting tested. I'm sorry if this post is inappropriate but I also want to emphasize that I'm not self-diagnosing. Symptoms may begin for no reason and have no explanation other than stress and anxiety. You don't even have to feel stressed for it to begin. ALS weakness would mean clinical weakness (inability to do something) not the feeling of weakness, twitching occurs after clinical weakness has begun, usually starts in one area, never has good/bad days, and pain does not set in until later stages.
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People wrote to us to tell us of their loved ones who fought this disease and PALS took the time to let us know their personal stories and how they live with ALS every day.

He said to me that I was standing in front of him with fairly normal reflexes, no muscle atrophy, no weakness etc. and from what I was telling him he was not concerned or thinking of ALS. Se hela listan på rehabmart.com ALS, better known as Lou Gehrig’s disease, Symptoms must be mitigated through equipment or therapy: Today, York uses a motorized wheelchair, although she can’t drive it on her own. Gallegos' ALS symptoms began with weakness in his hands. Benjamin Rasmussen / for NBC News At the nursing facility, Gallegos didn’t get the around-the-clock care he was used to.
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Though ALS currently has no cure, that doesn’t mean that there is no hope. In at least a few cases, people with ALS live for decades after their diagnosis. Some such patients find that the disease eventually stabilizes; though the symptoms they’ve experienced remain, no new symptoms develop.

Some people with I Sverige har cirka 750–850 personer diagnosen ALS. Det uppstår cirka 2–4 nya fall per 100 000 invånare varje år. Dubbelt så många män insjuknar i ALS upp till 65-årsåldern jämfört med kvinnor. Efter 70 års ålder finns ingen tydlig könsskillnad.