- What race does ALS affect the most?
- Where does ALS usually start?
- What does ALS spasticity feel like?
- How fast does ALS progress after first symptoms?
- How do you rule out ALS?
- What are the 3 types of ALS?
- Why is ALS becoming more common?
- What was your first ALS symptom?
- Can als be slow progressing?
- Can als be misdiagnosed?
- What triggers ALS disease?
- How do most ALS patients die?
- Who typically gets ALS?
- What does muscle weakness in ALS feel like?
- How long can you have ALS before diagnosis?
- Does muscle weakness come and go with ALS?
- What part of the body is affected by ALS?
What race does ALS affect the most?
Less is known about how ALS affects people of different racial and ethnic backgrounds.
Some studies suggest that ALS rates are higher among non-Hispanic Caucasians (whites) in Western countries compared with those of African, Asian, and Hispanic descent (minorities) (9–13)..
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.
What does ALS spasticity feel like?
Spasticity is one of the major symptoms of the illness. This is defined as muscle stiffness triggered by strong involuntary contractions. These contractions are violent, painful, and debilitating.
How fast does ALS progress after first symptoms?
And you’re right; it takes on average about nine to 12 months for someone to be diagnosed with ALS, from the time they first began to notice symptoms. Getting the proper evaluation in a timely way is important, especially since we have a drug, Rilutek, which has been shown to help delay the progression of ALS.
How do you rule out ALS?
ALS is primarily diagnosed based on detailed history of the symptoms and signs observed by a physician during physical examination along with a series of tests to rule out other mimicking diseases. However, the presence of upper and lower motor neuron symptoms strongly suggests the presence of the disease.
What are the 3 types of ALS?
This breakdown occurs in all three forms of ALS: hereditary, which is called familial; ALS that is not hereditary, called sporadic; and ALS that targets the brain, ALS/dementia.
Why is ALS becoming more common?
ALS affects people in all racial, social, and economic groups. This condition is also becoming more common. This may be because the population is aging. It could also be due to increasing levels of an environmental risk factor that hasn’t been identified yet.
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.
Can als be slow progressing?
In summary, lower limb-onset ALS has the potential to be a slowly progressive condition whether there is initial spread to the contralateral limb (as described in the ‘flail leg’ phenotype) or spread to the ipsilateral arm.
Can als be misdiagnosed?
AUSTIN – Lack of upper motor neuron signs on examination, presence of sensory symptoms, and absence of tongue fasciculations are common causes of amyotrophic lateral sclerosis (ALS) misdiagnosis, according to an investigation presented at the annual meeting of the American Association of Neuromuscular and …
What triggers ALS disease?
Chemical imbalance. People with ALS generally have higher than normal levels of glutamate, a chemical messenger in the brain and in the spinal fluid around nerve cells. High levels of glutamate are toxic to some nerve cells and may cause ALS.
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.
Who typically gets ALS?
Most people who develop ALS are between the ages of 40 and 70, with an average age of 55 at the time of diagnosis. However, cases of the disease do occur in people in their twenties and thirties. ALS is 20 percent more common in men than in women.
What does muscle weakness in ALS feel like?
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.
How long can you have ALS before diagnosis?
Total diagnostic time, defined as the time from symptom onset to confirmed diagnosis, has been reported to range from eight to 15 months in ALS (1–8).
Does muscle weakness come and go with ALS?
ALS has a gradual onset that’s painless. Progressive muscle weakness is the most common symptom.
What part of the body is affected by ALS?
ALS, or amyotrophic lateral sclerosis, is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord.