- How quickly does ALS progress?
- Does ALS come on suddenly?
- Can ALS patients gain weight?
- What was your first ALS symptom?
- How long does early stage ALS last?
- Does anyone survive ALS?
- Does ALS cause rapid weight loss?
- What does weakness feel like in ALS?
- Do ALS patients sleep a lot?
- What are the last days of ALS like?
- Why do ALS patients lose their voice?
- What does ALS feel like in the beginning?
- Where does ALS usually start?
- How do most ALS patients die?
- Do ALS patients lose weight?
How quickly does ALS progress?
The rate at which ALS progresses can be quite variable from one person to another.
Although the mean survival time with ALS is three to five years, some people live five, 10 or more years.
Symptoms can begin in the muscles that control speech and swallowing or in the hands, arms, legs or feet..
Does ALS come on suddenly?
Marked weakness of the ED with relatively mild weakness of the other muscles in the affected limb was a characteristic finding in both cases. It is unlikely that the disease process of ALS actually began suddenly.
Can ALS patients gain weight?
Based on the available literature, it is not clear whether patients with ALS should gain weight during their follow-up. It is likely that this recommendation should be adapted to the patient’s nutritional status, respiratory function, and physical abilities.
What was your first ALS symptom?
Typical early symptoms include tripping and falling; painless weakness in the legs, feet (also called foot drop), or ankles; hand weakness; slurred speech or trouble swallowing; muscle twitching or cramps in the arms, shoulders, or tongue; and difficulty holding the head up or maintaining good posture.
How long does early stage ALS last?
Gradually all muscles under voluntary control are affected, and individuals lose their strength and the ability to speak, eat, move, and even breathe. Most people with ALS die from respiratory failure, usually within 3 to 5 years from when the symptoms first appear.
Does anyone survive ALS?
ALS is fatal. The average life expectancy after diagnosis is two to five years, but some patients may live for years or even decades. (The famous physicist Stephen Hawking, for example, lived for more than 50 years after he was diagnosed.) There is no known cure to stop or reverse ALS.
Does ALS cause rapid weight loss?
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease resulting from the progressive degeneration of upper and lower motor neurons of the spinal cord, the brainstem and the cerebral cortex. In the course of the disease, 15-55% of patients suffer from clinically severe weight loss [1-4].
What does weakness feel like in ALS?
Muscle weakness (which is often only on one side of the body, such as one arm or one leg) as well as changes in the character of the individual’s voice (especially slurred words or slowness of speech).
Do ALS patients sleep a lot?
Strong feelings of being sleepy during daytime hours are much more common in amyotrophic lateral sclerosis (ALS) patients than the general public, and appear to be associated with poorer cognitive skills and greater behavioral problems, a study from China reports.
What are the last days of ALS like?
Caregivers reported that the most common symptoms in the last month of life included difficulty communicating (62%), dyspnea (56%), insomnia (42%), and discomfort other than pain (48%). Pain was both frequent and severe. One-third of caregivers were dissatisfied with some aspect of symptom management.
Why do ALS patients lose their voice?
As nerves are lost to the disease, the muscles they control become weak and tight. This causes dysarthria – the term used to describe slow, effortful, slurred speech, and breathy or hoarse voice. Weakening lung muscles affect speech as well.
What does ALS feel like in the beginning?
Early symptoms of ALS are usually characterized by muscle weakness, tightness (spasticity), cramping, or twitching (fasciculations). This stage is also associated with muscle loss or atrophy.
Where does ALS usually start?
ALS often starts in the hands, feet or limbs, and then spreads to other parts of your body. As the disease advances and nerve cells are destroyed, your muscles get weaker. This eventually affects chewing, swallowing, speaking and breathing.
How do most ALS patients die?
Most people with ALS die from respiratory failure, which occurs when people cannot get enough oxygen from their lungs into their blood; or when they cannot properly remove carbon dioxide from their blood, according to NINDS.
Do ALS patients lose weight?
ALS patients typically lose a significant amount of weight, both because their muscles atrophy from disuse and because they are physically unable to consume enough calories to maintain weight. Recent studies suggest that reduced appetite and an elevated metabolic level may also contribute to weight loss.