Als: Frequently Asked Questions
What is ALS?
Administrative Licence Suspension (also known as administrative licence revocation) is the temporary and almost immediate removal of the licence, if the driver refuses to provide a breath sample for an alcohol test, or if the test shows they have a BAC in excess of 80 mg%. This sanction is applied independent of a Criminal Code conviction, which also carries with it prohibitions from driving. Source: Beirness et al., 1997. Evaluation of the administrative licence suspension and vehicle impoundment programs in Manitoba. ...
Source: www.trafficinjuryresearch.com
Amyotrophic Lateral Sclerosis, also known as Lou Gehrig’s Disease, is a fatal, rapidly-progressing neuromuscular disease that affects hundreds of thousands of people worldwide. There is no known cause, no treatment, no cure and life expectancy is 2-5 years from time of diagnosis. It affects men and women equally, regardless of ethnicity, genetics or behavior. ...
Source: www.indestructiblefilm.com
ALS is the software used to program the APB-2400. ALS is Windows based calendar software that allows the user to set the schedule of lock & unlock times. The schedule is saved to a mini SD card to be inserted in the APB-2400 to implement the schedule
Source: www.automatedlock.com
Amyotrophic lateral sclerosis is a rapidly progressive disease that attacks the nerve cells responsible for controlling voluntary muscles. Eventually, patients lose their strength and ability to move their arms, legs and body. When muscles in the diaphragm and chest wall fail, patients cannot breathe without ventilatory support. Most people with ALS die from respiratory failure, usually within three to five years. The average survival time is 24-36 months. About 10 percent of patients survive for 10 years or more.
Source: www.rideforlife.com
Is ALS hereditary?
At least 10% of ALS cases are hereditary. This is called familial ALS. Generally, we define familial ALS as two or more cases in the same bloodline. In familial ALS, the disease is autosomal dominant, meaning that if a parent has ALS, their children have a 50% chance of inheriting the defective gene. While the risk of inheriting the defective gene is 50% for each child of an affected person, not all people with the defective gene will develop the disorder. ...
Source: www.rockinforacure.org
Is ALS painful?
Some of the pain ALS may cause are pressure sores, muscle aches or cramps, swelling feet, and muscle contractions.
Source: www.focusonals.com
Does The ALS Association fund ALS research?
The ALS Association is the largest private source of funding for ALS-specific research in the world. Over the last decade, we have committed close to $48 million to ALS research, seeking to identify the cause, means of prevention, and cure for ALS. The Association is currently overseeing approximately 100 different and diverse research projects. Through its world-class research program , The ALS Association is leading the search for a cure for ALS.
Source: www.alsa.org
Why ALS Consulting and not ALS Translations?
While translations make up the bulk of ALSC's business, ALSC also consults clients with respect to scientific endeavors and offers assistance in writing grant proposals, research papers, and patents.
Source: www.cyberg8t.com
Does ALS affect the mind?
There are many mixed opinions on this subject. Especially in current discussions. It is now known that some ALS patients do experience dementia, but it is unknown whether ALS was the cause of the dementia. Past ALS literature describes the mind as being "completely unaffected. "
Many current ALS specialists are starting to take a much closer look at this statement. Many are reconsidering.
Source: www.rockinforacure.org
What causes ALS?
The cause of ALS is unknown. Researchers know that an excess of a neurotransmitter called glutamate clogs the synapse of the nerve cell preventing transmission of neural impulses. The cause of this neurotransmitter problem remains a mystery.
Source: www.rockinforacure.org
Who gets ALS?
ALS occurs in both sexes and all races. Men are much more likely to get ALS than women. Older people are more likely to get ALS than younger people.
Source: www.rockinforacure.org
ALS usually strikes in late middle age; the late 50s is average or later in person’s life. Although, there have been cases of ALS in young adults and even in children. It was also happening as well as in very elderly people. Some genetic forms of ALS have their onset in youth as well. The truth is that men are somewhat more likely to develop ALS than are women. Studies suggest an overall ratio of about 1.2 men to every woman who develops the disorder of ALS. ...
Source: www.steadyhealth.com
What are the effects of ALS?
Because ALS frequently takes its toll before being positively diagnosed, many patients are debilitated before learning they have contracted ALS. The disease usually does not affect the senses - taste, touch, sight, smell, and hearing - or the mind. ALS wreaks a devastating effect on patients as well as their families. As they cope with the prospect of advancing disability and eventually death, it consumes their financial and emotional reserves. ...
Source: www.als.ca
Is there hope for people with ALS?
At the moment, there is a drug trial being conducted that may prolong life minimally. Research is looking to find not only the cause of the disease so that a cure can be developed but also other medications or treatments that can help until a cure is found. With improved knowledge about ALS, healthcare providers and families can help people living with ALS live life more fully. The services offered by the ALS Societies of Canada help improve the quality of life for those who live with ALS and their families.
Source: www.als.ca
Does ALS run in families?
ALS runs in families, because it shows a family history about 10 percent of the time. Several genes associated with ALS identify or at least mapped to a specific region of a chromosome.
Source: www.steadyhealth.com
Where is The ALS Association located?
The ALS Association's National Office is headquartered in Calabasas Hills, California. The Association has a nation-wide network of chapters and several dozen free standing support groups located throughout the United States carrying out the mission and activities of the organization at the local level. The ALS Association has representation in over 50 of the major markets in the United States.
Source: www.alsa.org
What is The ALS Association?
The ALS Association is the only national not-for-profit health agency dedicated solely to the fight against ALS. The mission of The ALS Association is to lead the fight to cure and treat ALS through global, cutting-edge research, and to empower people with Lou Gehrig’s disease and their families to live fuller lives by providing them with compassionate care and support.
Source: www.alsa.org
Is BFS related to ALS?
No, although exhibiting some of the same symptoms, ALS and BFS are two distinctly separate illnesses.
Source: www.nextination.com
What does "ALS" mean?
Alternate Line Service. This service provides you with an additional phone number for your phone so that you may separate charges for business and personal calls.
Source: nextel.andlogistix.com
Why choose ALS?
Our treatments are performed by medically licensed professionals in accordance with the Ohio State Medical Board’s regulations. Hair removal is what we do best. Our technicians have over 7 yrs combined experience and have performed over 12,000 treatments. We perform Hair Removal with one of the industries most trusted lasers. The Candela GentleLASE is an Alexandrite laser that is extremely effective for permanent hair reduction. ...
Source: www.als-laser.com
How Is ALS Diagnosed?
At present 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;
Source: www.focusonals.com
ALS is a very difficult disease to diagnose. To date, there is no one test or procedure to ultimately establish the diagnosis of ALS. It is through a clinical examination and series of diagnostic tests, often ruling out other diseases that mimic ALS, that a diagnosis can be established. ...
Source: www.gwdocs.com
When Was ALS First Discovered?
ALS/MND was first described in 1869 by Jean-Martin Charcot , a trail- blazing French neurologist.
Source: www.focusonals.com
What Is ALS/MND?
Amyotrophic 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. ...
Source: www.focusonals.com
Amyotrophic Lateral Sclerosis or Motor Neurone Disease is a progressive, usually fatal neuromuscular disease. It attacks motor neurones in the spinal cord and lower brain which transmit signals from the brain to the voluntary muscles throughout the body. When motor neurones die as a result of ALS/MND, the ability of the brain to control muscle movement is lost. When muscles fail to receive messages, they weaken and waste away (atrophy). ...
Source: www.zazangels.com
HOW IS ALS/MND DIAGNOSED?
At present there is no definitive means of diagnosis of ALS/MND. Most diagnoses are made by eliminating all other possibilities - ailments with symptoms resembling those of ALS/MND. Neurologists use a number of clinical tests to establish a profile, including blood testing, MRI (Magnetic Resonance Imaging) scans and EMGs (Electro Myographs).
Source: www.zazangels.com
What is ALS Film Fund?
Through creative and accessible means, ALS Film Fund is committed to educating, inspiring and invoking change for the future benefit of ALS patients worldwide. It was started by Ben Byer and his sister Rebeccah Rush in 2007 as the production company for Indestructible , as well as future projects that will further our mission. Our goal for the company is to create more film, works of art, books, theatrical productions and any other creative vehicle for raising awareness for ALS until a cure has been found. ...
Source: www.indestructiblefilm.com
What are the forms of ALS?
Three classifications of ALS have been described: Sporadic - the most common form of ALS in the United States - 90 to 95% of all cases. Familial - occurring more than once in a family lineage (genetic dominant inheritance) accounts for a very small number of cases in the United States - 5 to 10% of all cases. Guamanian - an extremely high incidence of ALS was observed in Guam and the Trust Territories of the Pacific in the 1950's. The most common form of ALS in the United States is "sporadic" ALS. ...
Source: www.gwdocs.com
How is ALS treated?
Present treatment of ALS includes one drug, riluzole (Rilutek©) and is aimed at symptomatic relief, prevention of complications and maintenance of maximum optimal function and optimal quality of life. Most of this, in the later stages, requires substantial physical caregiving. Click here for more information on Rilutek. ...
Source: www.gwdocs.com
How can people get more information about ALS and The ALS Association?
The ALS Association has a toll-free information and referral service available to patients, caregivers and family members, staffed by The ALS Association Patient Service Coordinators. The ALS Association Information and Referral number is 1-800-782-4747. To reach The ALS Association's Patient Services department by e-mail, contact alsinfo@alsa-national.org . All media inquiries should be directed to The ALS Association's Media Relations department, 818-880-9007, x241 ( mediarelations@alsa-national.org ).
Source: www.alsa.org
