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Lou Gehrig's Disease
Lou Gehrig's disease is a fatal, progressive disease that affects the nerves that control a person’s voluntary muscle movement. Individuals afflicted with the disorder lose the capacity to control and initiate voluntary movements.
64 Questions
What happened to lou gehrig with als disease?
Lou Gehrig's diagnosis was confirmed on June 19, 1939. It was on his 36th birthday.
How fast does Lou gehrigs disease progress?
Between 3-5 years
Sometimes less depends on how serious it is.
Only 20% of people lived more than 5 years.
Some are still alive today such as Stephen Hawking (Similar disease)
Is Lou Gehrig's disease a genetic disorder?
It is caused by a prion. This an infectious protein not a virus.
Is there a difference between ALS and Lou Gehrig's disease?
Because Lou Gehrig (Yankee's baseball player) developed the disease and still managed to thank everybody for his great life he was given.
Does Lou Gehrig's Disease affect men only?
No, Parkinson's disease can affect both men and women. Although it is thought to have a higher incidence in men, Parkinson's is caused by an imbalance levels of neurotransmitters in the brain, which both men and women have.
What is the life expectancy of someone with Lou Gehrig's disease?
Approximately 5,600 people in the U.S. are diagnosed with ALS each year. The incidence of ALS is two per 100,000 people, and it is estimated that as many as 30,000 Americans may have the disease at any given time.
How did Stephen Hawking' s get Lou Gehrig's disease?
Scientists have not been able to find a cause for the disease although they believe it could be caused by a virus or defects to DNA, the immune system, or enzymes found in one's body. These defects may be caused by pesticides or other types of toxins/poisons. Much more research must be done before a true cause will be found.
Was Lou Gehrig the first person to be diagnosed with ALS?
In the year 1824 a scientist named Charles Bell published a paper discussing this previously unknown disease called Amyotrophic Lateral Sclerosis. In 1939, baseball player Lou Gehrig contracted this disease. Since he was so well known at the time, the disease was nicknamed the Lou Gehrig Disease.
What causes fingers to turn black?
Normally parts which are bruised turn black. You probably jammed your thumb somewhere. It is the blood inthe bruised tissue that makes it look black.
When Lou Gehrig began showing symptoms of the disease is not really known but his performance on the field started to drop off during the 1938 season and he also complained about being tired a lot. He was diagnosed with amyotrophic lateral sclerosis in June, 1939 and passed away on June 2, 1941. So he lived 2 years after being diagnosed with the disease and may have been showing symptoms a year before he was diagnosed.
Lou Gehrig was raised in a German Lutheran family, and his faith played a role in his upbringing. However, throughout his life, Gehrig was known to be more private about his religious beliefs and did not publicly emphasize his faith in the same way some other athletes did. His focus was primarily on baseball, family, and his legacy rather than on religious expression. After his diagnosis with ALS, he famously delivered a heartfelt farewell speech that reflected his character and resilience rather than religious themes.
What does Lou Gehrig's disease feel like?
The earliest sign of Lou Gehrig's disease is most often weakness in the arms or legs, at first usually more pronounced on one side than the other.
It is called ALS, which stands for "Amyotrophic Lateral Sclerosis." It is also known as "Lou Gehrig's Disease", and is sometimes called Maladie de Charcot.
You have to do a minute oral report on Lou gehrigs disease?
Click on the 'Lou Gehrig's Disease' link below to help you with your research.
How does Lou Gehrig's disease affect your daily life?
AFFECTING THE LATERAL COLUMNS OF SPINAL CORD AND MEDULLA OF BRAIN,IT CAUSES PROGRESSIVE MUSCULAR PARALYSIS, also affects arterial walls..
Expected lifespan with Lou garricks disease?
It would depend on the patient, but from my family experience 2-4 years after diagnosis.
Is Lou Gehrig's Disease Inherited?
"Familial", ALS suggests the disease is inherited, although no heredity pattern exists in the majority of ALS cases. About 5 to 10 percent of all ALS patients appear to have a genetic or inherited component. In those families, 50 percent of the all offspring are expected to have the disease.
Most who develop ALS are between the ages of 40 and 70. There have been many cases of the disease attacking teenagers, though generally, ALS occurs in greater percentages as men and women grow older.
It was once believed that men developed ALS more frequently than women. That no longer appears to be the case, and today both sexes are affected in nearly equal numbers.
Symptoms of Lou Gehrig's DiseaseEarly symptoms vary with each individual, but they usually include tripping, dropping things, abnormal fatigue of the arms and/or legs, slurred speech, muscle cramps and twitches, and involuntary periods of laughing or crying.With the hands and feet affected first, it causes difficulty in walking or using the hands for the activities of daily living, such as dressing, washing and buttoning clothes.
Since ALS affects only motor neurons, the senses of sight, touch, hearing, taste and smell, muscles of the eyes and bladder are generally not affected.
As the weakening and paralysis continues to spread to the muscles of the trunk of the body, it eventually affects swallowing, chewing and breathing. When the breathing muscles are affected, the patient may require permanent ventilatory support to survive. The mind is not impaired and remains sharp, despite the progressive degenerating condition of the body.
Diagnosis of Lou Gehrig's DiseaseElectromyography (electrical studies of muscle) is often performed to confirm the disease. A biopsy (removal of a small piece of tissue) of muscle tissue may also been performed if the diagnosis is in doubt. Treatment of Lou Gehrig's DiseaseAlthough there is no cure for ALS, much can be done to help patients live more productively and independently. Physical therapy and rehabilitation techniques can help patients learn how to work around the weakness and functional disability caused by the disease. Patients may benefit from braces or a walker to improve mobility.2 diseases of the system and how they affect the system?
polymyositis (directly effect muscle)
dematomyositis (directly effect muscle)
eaton-lambert syndrome (indirectly)
kennedy syndrome (indirectly)
myotonic dystrophy (indirectly)
tenaie solium infection (directly)
duchenne's muscular dystrophy
becker's muscular dystrophy
carnitine palmitoyl transferase deficiency
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