Emory ALS Center: What is ALS?
BlogMetaFinder Search for als diseaseEmory ALS Center: What is ALS?Amyotrophic Lateral Sclerosis (ALS) is also known as Motor Neuron Disease, Lou Gehrig's Disease, and Charcot's Disease (in Europe). ALS is a disease of "motor neurons", the cells ... Mon, 28 Emory ALS Center: ALS ResearchNine members of the Emory ALS Center Team are attending the International Motor Neuron Disease Association meeting in Toronto, Canada, where the latest developments in clinical ... Mon, 28
Related QuestionsWhat Is ALS?
Patient Services Frequently Asked Questions - The ALS Associ...Amyotrophic Lateral Sclerosis (ALS) is a motor neuron disease, first identified in 1869 by the noted French neurologist Jean-Martin Charcot. Although the cause of ALS is not completely understood, the 1990's have brought a wealth of new scientific understanding about the physiology of this disease.
Related QuestionsWhat Is ALS/MND?
Frequently Asked QuestionsAmyotrophic Lateral Sclerosis, a.k.a Motor Neuron Disease-is a rapidly progressive, fatal neuromuscular disease. It attacks motor neurons in the spinal cord and lower brain which transmit signals from the brain to the voluntary muscles throughout the body. When motor neurons die as a result of ALS, the ability of the brain to control muscle movement is lost. When muscles fail to receive messages, they weaken, atrophy, and die. There is no known cure.
Related QuestionsHow Is ALS Diagnosed?
Frequently Asked Questionspresent there is no definitive means of diagnosis of ALS/MND. Most diagnoses are made by eliminating all other possibilities--ailments whose symptoms resemble those of ALS/MND. Neurologists use a number of clinical tests to establish a profile, including blood testing, EMG, MRI, etc;
Related QuestionsIs ALS painful?
Frequently Asked QuestionsSome of the pain ALS may cause are pressure sores, muscle aches or cramps, swelling feet, and muscle contractions.
Related QuestionsWhat is ALS - ALS Descriptioncurren; back to top ¤ALS stands for Amyotrophic Lateral Sclerosis, sometimes called Lou Gehrig's disease. It is a rapidly progressive and fatal neuromuscular disease that is characterized by degeneration of a select group of nerve cells and pathways (motor neurons) in the brain and spinal cord. This loss of motor neurons leads to progressive paralysis of the voluntary muscles. The heart is not a voluntary muscle, and therefore, remains unaffected by the disease.Related Questions
What services are available at the Carolinas ALS Center?
ALS Frequently Asked Questions - - Brain And Spine - Carolin...The Carolinas ALS Center provides a full spectrum of medical, therapeutic and support specialists in a hospital-based outpatient setting. It is also a leading resource for patient and family education materials. Patient support groups throughout the region are invited to affiliate with Carolinas ALS Center to consolidate efforts for improving patient services. Patients can sample or borrow devices capable of synthesizing or augmenting speech from the center's Communication Laboratory.
Related QuestionsHow do I make an appointment at the Emory Clinic Ambulatory Surgery Center?
STRONG>Ambulatory Surgery Center - Frequently Asked Question...Your physician or surgeon will schedule your procedure at the Emory Clinic Ambulatory Surgery Center.
Related QuestionsAmyotrophic Lateral Sclerosis ALS: rockin for a cureAmyotrophic Lateral Sclerosis (ALS) is a fatal neuromuscular condition characterized by progressive muscle weakness, muscle wasting, fasciculations and increased reflexes, resulting in total paralysis of all voluntary muscles. ALS is a rapidly progressive, fatal neuromuscular disease that attacks motor neurons in the spinal cord and lower brain, which transmit signals from the brain to the voluntary muscles throughout the body.Related Questions
Patient Services What Is ALS?
Patient Services Frequently Asked Questions - The ALS Associ...Amyotrophic Lateral Sclerosis (ALS) is a motor neuron disease, first identified in 1869 by the noted French neurologist Jean-Martin Charcot. Although the cause of ALS is not completely understood, the 1990's have brought a wealth of new scientific understanding about the physiology of this disease.
Related QuestionsWhat Are The Symptoms Of ALS/MND?
Frequently Asked QuestionsThe groups of muscles affected and the order in which they are affected varies from one person to another. Early symptoms usually include tripping, dropping things, abnormal fatigue of the arms and/or legs, slurred speech, muscle cramps and twitches and uncontrollable periods of laughing or crying. The hands and feet may be affected first, causing difficulty in walking or using the hands for the activities of daily living such as dressing, washing and buttoning clothes.
Related QuestionsWho Is Liable To Get ALS/MND?
Frequently Asked QuestionsAnyone can get ALS/MND. Most who develop ALS/MND are between the ages of 40 and 70. There are, however, cases of the disease attacking persons in their twenties and thirties. Generally though, ALS/MND occurs in greater percentages as men and women grow older. ALS/MND strikes men slightly more frequently than women. About one in 800 adult men, and one in 1,200 adult women die of ALS/MND. ALS/MND occurs throughout the world with no racial, ethnic or socioeconomic boundaries.
Related QuestionsAre There Different Types Of ALS/MND?
Frequently Asked QuestionsThere are three common classifications, and numerous sub-categories: Sporadic: the most common form of ALS/MND Familial: less than 10% of ALS/MND cases suggest genetic inheritance Guamanian: a high number of cases of ALS/MND occur in Guam and the Trust Territories of the Pacific
Related QuestionsWhat Causes ALS/MND?
Frequently Asked QuestionsThe cause of ALS/MND is not yet known. While many theories are being researched, at present neither a cure nor a means of prevention is known. In 1993, scientists announced in a paper published in the British journal "Nature" that they had isolated the gene associated with about 20% of the cases of the inherited form of the disease.
Related QuestionsCan You "Catch" ALS/MND?
Frequently Asked QuestionsALS/MND cannot be "caught" - it is not contagious. Though some scientists believe it is possible that ALS/MND is caused by a slow-acting or latent "virus", there is absolutely no fear that it is contagious: there is no increased incidence among medical personnel who deal with ALS/MND patients.
Related QuestionsIs There Hope For People With ALS/MND?
Frequently Asked QuestionsALS/MND wreaks a devastating effect on patients as well as their families. As they struggle to cope with the prospect of advancing disability and death, it consumes their emotional and financial reserves. It is a costly disease in its later stages, demanding both extensive nursing care and expensive equipment. But there is always hope. Recent medical discoveries have led to new drugs which seem to slow the progression of the disease.
Related QuestionsAmyotrophic Lateral Sclerosis (ALS) and Soccer: Is there a Connection?
NetofCare E-Newsletter - October 2003Early this year, there was a media report of a suspected cluster of ALS among Italian soccer players. This important scientific observation requires scientific study although, at this time, it is not clear exactly what the possible association between ALS and soccer playing may be. The Miami Herald and the National Italian American Foundation have announced and published story updates.
Related QuestionsWhat about the use of minocycline in other diseases like stroke and ALS?
Multiple Sclerosis Society of Canada - Minocycline FAQ, Octo...Minocycline has been tested to treat other diseases like stroke and ALS with varied results. In MS, researchers are looking at minocycline to influence a target that is very specific to MS. Preliminary research has demonstrated that minocycline has great potential to slow down the progression of MS. This work has led to the development of a new $4 million phase III clinical trial involving 200 people and funded by the MS Society of Canada’s related MS Scientific Research Foundation.
Related QuestionsCan creatine help people with ALS and what are the potential side effects?
Patient Services Frequently Asked Questions - The ALS Associ...with any medication or dietary supplement, it is important to check with the physician managing your ALS care to discuss the pros and cons of adding any new drug or supplement. Creatine is a dietary supplement and is sold in most health food stores. A variety of companies produce creatine. Because it is not a drug, creatine does not fall under the control of the FDA for product claims or manufacturing purity.
Related QuestionsHow many people have ALS?
FRONTLINE: so much so fast: what's als? | PBSIt is estimated that 30,000 people in the U.S. have ALS at any given time, with approximately 5,600 new cases diagnosed annually. More than 5,000 people die from the disease each year.
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