- Can someone be misdiagnosed with ALS?
- What can mimic ALS?
- How quickly does ALS progress?
- Can ALS progress very slowly?
- What triggers ALS disease?
- When should I worry about muscle twitching?
- What does ALS feel like in the beginning?
- Can ALS affect all limbs at once?
- Where does ALS usually start?
- How do most ALS patients die?
- Does ALS start with muscle twitching?
- What are my odds of getting ALS?
- Does ALS show up on blood work?
- Does ALS come on suddenly?
- What was your first ALS symptom?
- What does ALS muscle weakness feel like?
- Do early ALS symptoms come and go?
- What does ALS in hands feel like?
- Does ALS make you tired?
- How long does early stage ALS last?
- Do ALS patients sleep a lot?
Can someone be misdiagnosed with ALS?
Yes, up to 40% of patients are initially told they have another disease, and then it turns out they have ALS.
Many conditions can mimic ALS.
This type of a diagnostic error is called a false-negative error of diagnosis..
What can mimic ALS?
A number of disorders may mimic ALS; examples include:Myasthenia gravis.Lambert-Eaton myasthenic syndrome.Lyme disease.Poliomyelitis and post-poliomyelitis.Heavy metal intoxication.Kennedy syndrome.Adult-onset Tay-Sachs disease.Hereditary spastic paraplegia.More items…
How quickly does ALS progress?
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.
Can ALS progress very slowly?
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.
What triggers ALS disease?
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.
When should I worry about muscle twitching?
You should see a doctor for muscle spasms if you encounter any of the following situations: Any muscle spasms that are occurring regularly. Muscle spasms that are not resolving on their own with rest, hydration, and proper nutrition. Any pain or injury that you have as a result of a muscle spasm, especially back spasms.
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.
Can ALS affect all limbs at once?
One of the first signs of ALS is weakness on one limb, the face or the tongue. Eventually the weakness spreads to all of the limbs and then the other muscles in the body that control functions important for survival.
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.
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.
Does ALS start with muscle twitching?
The onset of ALS may be so subtle that the symptoms are overlooked. The earliest symptoms may include fasciculations (muscle twitches), cramps, tight and stiff muscles (spasticity), muscle weakness affecting a hand, arm, leg, or foot, slurred and nasal speech, or difficulty chewing or swallowing.
What are my odds of getting ALS?
It’s rare, affecting about 5.2 people per 100,000 in the U.S. population, according to the National ALS Registry. Because of the seemingly random nature of the condition, it’s hard for researchers to pinpoint who might have a greater chance of getting it.
Does ALS show up on blood work?
Blood and Urine Tests These won’t detect ALS, but common lab tests can be used to rule out other diseases that have the same kinds of symptoms.
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.
What was your first ALS symptom?
Initial Symptoms of ALS Bulbar onset usually affects voice and swallowing first. The majority of ALS patients have limb onset. For these individuals, early symptoms may include dropping things, tripping, fatigue of the arms and legs, slurred speech and muscle cramps and twitches.
What does ALS muscle weakness feel like?
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 early ALS symptoms come and go?
ALS symptoms are progressive meaning the symptoms get worse over time and often develop very quickly. That said there are some cases in which symptoms, such as difficulty swallowing, can get better for a period of time.
What does ALS in hands feel like?
If you or a loved one are experiencing any of the classic signs of ALS – muscle twitches, decrease in grip strength, or weakness in the upper limbs – you may already be combing the Internet for information, worried that ALS is the cause.
Does ALS make you tired?
Although the course of ALS is unpredictable, fatigue is one outcome that is predictable, resulting from muscle weakness and spasticity. Fatigue can range from mild lassitude to extreme exhaustion. People often complain of tiredness, dwindling strength, and lack of energy.
How long does early stage ALS last?
Most people with ALS die from respiratory failure, usually within 3 to 5 years from when the symptoms first appear. However, about 10 percent of people with ALS survive for 10 or more years.
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.