After the golf episode, the left toe dragging occurred when I played tennis and after a long walk.
Risk factors Here are some of the risk factors associated with MND. In the United States U. SMA is also known to be an inherited condition. After the age of 40 years, the risk rises significantly, although it is still very small. ALS is most likely to appear between the ages of 55 and 75 years.
Men are more likely to develop an MND. Some experts have linked military experience to a higher chance of developing the disease.
Studies have found that professional footballers are more likely to die from ALS, Alzheimer's diseaseand other neurodegenerative diseases, compared with other people. This implies a possible link with recurrent head trauma and neurological disease. Diagnosis The treatment of motor neuron diseases is mostly about managing symptoms and enabling comfortable living.
In the early stage, MND can be hard to diagnose, because the signs and symptoms are common to other conditions, such as multiple sclerosis MSan inflamed nerve, or Parkinson's disease. A primary care physician will normally refer the patient to a neurologist, a doctor specialized in the diagnosis and treatment of diseases and conditions of the nervous system.
The neurologist will start with a complete history and physical exam of the neurologic system. Other tests may be helpful. Blood and urine tests: These analyses can rule out other conditions and detect any rise in creatinine kinase.
This is produced when muscle breaks down, and it is sometimes be found in the blood of patients with MND. This cannot detect an MND, but it can help rule out other conditions, such as strokebrain tumorbrain circulation problems, or abnormal brain structure.
These are often performed together. An EMG tests the amount of electrical activity within muscles, while NCS tests the speed at which electricity moves through muscles. Spinal tap, or lumbar puncture: This analyzes the cerebrospinal fluid, the fluid that surrounds the brain and spinal cord.
If the doctor thinks the patient may have a muscle disease, rather than MND, a muscle biopsy may be performed.If at least one parent is a bearer of the disease, two out of four off the progeny will be a bearer of the disease. If both parents are bearers of the disease, one out of four kids will non be a bearer, two out of four of the kids will be a bearers of the disease, and on out of four of the kids will really hold the Tay-Sachs disease (www.
Purpose of Website: This website is created to inform people of Lou Gehrig's Disease also know as ALS. This disease is very dangerous and needs to be taken more seriously.
What is ALS What causes AlS Who gets AlS Statistics Discuss history,(you many share the story of Lou Gehrigs). You may add to this. 2nd the physical side of the health issue and include risk factors, symptoms/presentation, how it affects various systems of the body, and prognosis. Lou Gehrig was stricken with the spinal disease amyotrophic lateral sclerosis (ALS) and was forced to retire from baseball early in the season.
ALS has come to be known as Lou Gehrig's disease. Gehrig was elected into the Baseball Hall of Fame in and died from ALS in Lou Gehrigs Disease Essay Health: Disease (ALS) Brooke Palin ENC Amyotrophic lateral sclerosis; Motor neuron disorders are far from rare: Parkinson’s disease, multiple sclerosis, and a variety of lesser diseases all come under that heading.
Lou Gehrig's disease is also called amyotrophic lateral sclerosis, or ALS. Amyotrophic means that muscles have lost their nourishment. When this occurs, they become smaller and weaker/5(1).