Lou Gehrig Disease
Lou Gehrig disease has no cure, but treatments for the disease can help control the symptoms. A diagnosis can be confirmed through muscle biopsy and nerve biopsy. Although the disease has no cure, medications and treatments can help control symptoms and slow down the progression of the disease. If you are concerned about your chances of surviving Lou Gehrig’s disease, you should consult your doctor.
How does someone get Lou Gehrig’s disease?
Lou Gehrig’s disease affects the nerves that control muscle movement. Symptoms of this disease may include difficulty swallowing, choking, and respiratory problems. If left untreated, this condition can progress to the point where people cannot function normally. The disease can also affect communication and balance. It is not known how Lou Gehrig’s disease develops, but treatment may slow down the symptoms and delay the disease’s progression.
ALS starts with motor neurons dying off in the brain and spinal cord. Once these nerve cells die, the muscles can no longer receive messages from the brain and therefore become paralyzed. Even though someone with this condition may lose their ability to move, they still have the ability to hear, smell, and feel touch. This disease is not caused by a stroke or other serious illness. Symptoms of ALS vary from person to person, but usually start out with muscle weakness and twitching. As the disease progresses, breathing becomes increasingly difficult.
How long can someone live with Lou Gehrig disease?
Lou Gehrig’s disease (ALS) is a degenerative disorder that deteriorates motor neurons, which control muscles. This leads to paralysis. Most people who suffer from ALS do not have obvious symptoms at first. Instead, they may begin to experience slurred speech, muscle weakness, and twitching. Although there is no cure for ALS, treatment options can help control symptoms and slow its progression.
Currently, the average life expectancy for ALS patients is between three and five years. However, some patients may live longer. About 10 percent of people with the disease live more than 10 years, and around five percent live for over 20 years. Stephen Hawking, a famous ALS patient, lived for 55 years after being diagnosed. The disease can also progress more slowly in younger patients.
Is ALS always fatal?
Amyotrophic lateral sclerosis (ALS) is a devastating neurological disease that attacks the motor neurons that control voluntary muscle movement. The disease affects both the upper and lower motor neurons of the brain and spinal cord. Without these nerves, muscles can’t move, which ultimately leads to paralysis. Although there is no cure for ALS, treatment may slow its progression and improve overall function.
The symptoms of ALS vary from person to person. Often, patients will notice a gradual deterioration of their motor function in the upper and lower extremities. They may also notice twitches or weakness in a specific arm or leg and slurred speech. Ultimately, the disease is fatal.
Can Lou Gehrig’s disease be cured?
There is no cure for Lou Gehrig’s disease, but there are several therapies to slow down the progression. One of these therapies is called a combination therapy. The combination therapy is a combination of therapy and medication that can slow down the disease’s progression. The rate of progression can vary from person to person. If you’re concerned that you have the disease, your doctor will perform several tests, including blood tests and neurological tests.
Research is a key to developing treatments for the disease. Researchers at Oregon State University have been able to stop the progression of ALS in mice for almost two years. Their results are encouraging, since the mice with the disease now live close to normal lifespans. While a cure for ALS is still years away, recent advances in science have opened up many avenues for treatments.
How can you avoid getting ALS?
While there is no known cause of ALS, studies have linked certain genetic mutations to the disease, including the C9orf72 gene. This gene has also been linked to frontotemporal dementia. Some scientists believe the two disorders are related. It is not known whether environmental factors can trigger the disease.
There are several ways to protect your immune system. A good diet and adequate sleep are recommended. These can help prevent or minimize the symptoms of ALS. In addition, it is important to discuss your personal values, your life goals, and any advanced medical directives with your healthcare team. You do not have to make all decisions at once; you can discuss these issues with your medical team as you experience symptoms of the disease. You should also know the side effects of any new medicines or treatment options.
ALS is a degenerative disease that affects millions of people around the world. While most people develop the disease during their late fifties or early sixties, it can also develop at any age. While men are slightly more susceptible than women, ALS can affect people of all races and ethnicities. In the United States, the disease is more common in Caucasians and non-Hispanics.