ALSTDF :: Home Dedicated to finding therapies for amyotrophic lateral sclerosis. Contains descriptions of the disease and the foundation. http://www.als.net/
Extractions: Last night all of us in the ALS community lost a dear friend and a personal hero of mine. Will Hubben, a true leader in the ALS world, passed away peacefully with his wife Mary, family, and friends. Will Hubben was the creator and editor of the ALS Research Digest, a leader, and a friend to everyone working to cure ALS. HIS BROTHER'S KEEPER: A STORY ABOUT ALSTDF'S FOUNDER
Extractions: Contact Us Members of the Group All Products Books Journal Article eBooks Alphabetical Listing Journals by Subject Advertising Customer Services ... eBooks Instructions for Authors: ***Note to Authors: please make sure your contact address information is clearly visible on the outside of all packages you are sending to Editors. Editorial policy Amyotrophic Lateral Sclerosis and other motor neuron diseases is a high-quality quarterly journal which will cover all aspects of ALS and related disorders. It will include: Original reports and reviews can be up to 10,000 words in length. Black-and-white illustrations are welcomed (see below). Please contact the Editor to discuss the suitability of topics. Case reports and other short reports should be approximately 1500 words long, with no more than 15 references. Correspondence items should be no more than 1000 words in length, with 1 figure or table. Point-counterpoint items and book reviews will normally be commissioned by the Editor, but suggestions are welcomed.
ALS - Lou Gehrig's Disease - 916.979.9265 A nonprofit organization dedicated to providing education, information and support services to ALS (Lou Gehrig's disease) patients and their families. http://www.alssac.org
Extractions: (advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Patient Education Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Emergency Medicine Neurology Last Updated: May 16, 2003 Rate this Article Email to a Colleague Synonyms and related keywords: ALS, Lou Gehrig disease, Lou Gehrig's disease, Charcot disease, Charcot's disease AUTHOR INFORMATION Section 1 of 11 Author Information Introduction Clinical Differentials ... Bibliography Author: Kathleen Clem, MD , Chief, Associate Professor, Department of Surgery, Division of Emergency Medicine, Duke University Medical Center Coauthor(s): Joel C Morgenlander, MD , Clinical Chief, Associate Professor, Department of Internal Medicine, Division of Neurology, Duke University Medical Center Kathleen Clem, MD, is a member of the following medical societies: American College of Emergency Physicians , and Society for Academic Emergency Medicine Editor(s): Roy Alson, MD, PhD, FACEP, FAAEM
Extractions: (advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Patient Education Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Neurology Neuromuscular Diseases Last Updated: March 3, 2004 Rate this Article Email to a Colleague Synonyms and related keywords: ALS, Lou Gehrig disease, Lou Gehrig's disease, Charcot disease, Charcot's disease, motor neuron disease AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography Author: Fernando Dangond, MD , Associate Neurologist, Brigham and Women's Hospital; Assistant Professor, Department of Neurology, Harvard Medical School Fernando Dangond, MD, is a member of the following medical societies: American Academy of Neurology American Association for the Advancement of Science American Association of Immunologists , and American Medical Association Editor(s): Donald B Sanders, MD , Laboratory Director, Professor of Medicine (Neurology), Division of Neurology, Duke University Medical Center;
Focus On ALS Information and inspiration related to amyotrophic lateral sclerosis. http://www.focusonals.com/
Extractions: Midi: "No Matter What" Home What Is ALS? Symptoms Diagnosis ... Search MEDLINEplus Welcome to Focus on ALS which is a website created to provide information about the disease Amyotrophic Lateral Sclerosis. It is also known as motor neuron disease (MND) or Lou Gehrig's disease named after the famous baseball player who died in 1941. To learn more about ALS, you can start with the What is ALS? or FAQ pages. My name is Debbie Tope. I live in Baltimore, Ohio and have been living with ALS for 10 years. I was officially diagnosed in September of 1995 but I started showing symptoms in late 1993. If you would like to read a more detailed history of my life with ALS, you can read My Story I started Focus on ALS in 1996 and have continued to add to it until it now has over 700 pages. So it is my hope that I have all the information that you are looking for. I update my News Center pages as often as news is released pertaining to ALS. I subscribe to many sources for news so that Focus on ALS can be your one source for the latest ALS news. I update the entire website at least weekly so check back often. I have added a new Guestbook and Message Board to my site. I am hosting both myself which means that I will have more control over them. There will no longer be popup ads, there will be no ads to clutter the page, loading times should be quicker, and hopefully I can eliminate the trash postings. So feel free to sign the
Extractions: Visit MDA's ALS Division Web site for more information. Facts About ALS Clinical Trials Are Focus of MDA ALS Conference ALS Meeting Continues With Nitty-Gritty of Clinical Trials as Focus How the MDA Clinic Can Make a Difference ... Respiratory Care and "With Strength and Courage" Listing of MDA ALS Research and Clinical Centers in U.S.
Home Page Information about the organization as well as amyotrophic lateral sclerosis, ways to improve daily life with ALS, and an opportunity to donate to a worthy cause. http://als-curtisvancefoundation.org
Extractions: Memorial Orchard The Curtis R. Vance Foundation Donate Now The Curtis R. Vance Foundation is a nonprofit corporation, whose purposes include but are not limited to public education and funding of research for a cure for amyotrophic lateral sclerosis, ALS, commonly known as Lou Gehrigs disease, and providing assistance to the victims of the disease and their families. The Curtis R. Vance Foundation was created by Curtis Vance and his wife and caregiver, Heidi, in the winter of 1999. Diagnosed with familial ALS in December, 1998 at the age of 25, Curtis died in December 1999 as a result of respiratory failure. Throughout the time that Curtis lived with ALS, he remained positive that a cure would be found in his lifetime, and simultaneously lived each day as though it could be his last. He learned how to live while he prepared to die. His humor, love, and generosity flowed out of him and into every person who met him, both before and during his illness. Six months after the diagnosis, he questioned Heidi with a smile and a tear, "Why cant you find the cure?" And, during one of his last days, he declared to her, "I pray that no one else in my family, or in the world, will ever feel the way I do now." Although mentally strong and emotionally healthy, Curtis was physically exhausted. He could no longer move his legs and arms, breathe on his own, or eat and drink without the aid of a feeding tube. His voice was soft and slurred, and since his facial muscles had recently deteriorated, a smile was almost an impossible task. But, one could still sense his spirit in his eyes, and it is his spirit that has pushed 25-year-old Heidi forward since the day Curtis left his riddled body. When her days of physically caring for Curtis came to a halt, she began dedicating the hours to their foundation, and hopes that someday she can fulfill her husbands dreams.
Facts About ALS | MDA Publications Updated 10/03. Facts About amyotrophic lateral sclerosis (ALS) Muscular Dystrophy Association. WHAT IS amyotrophic lateral sclerosis? http://www.mdausa.org/publications/fa-als.html
Extractions: Muscular Dystrophy Association Introduction What is Amyotrophic Lateral Sclerosis? What Happens to Someone With ALS? What Happens to the Nervous System in ALS? ... MDA Is Here to Help You Dear Friends : When I learned in 1994 that I had amyotrophic lateral sclerosis, my world changed. I was in my early 50s, had a good career with the U.S. Small Business Administration, and was a husband and father. Suddenly, I faced a serious disease that would affect every aspect of my life. Glenn Harwood I decided my best weapon in this battle would be attitude. I've met every challenge ALS has presented with an approach that's unbeatable: I can do it, I will do it. With that conviction, I have a full and rewarding life with the help of a power wheelchair, a voice synthesizer and lots of e-mail. I've continued working, traveling and learning. I have wonderful allies in this fight: a fantastic family, including my wife, Fran, our two children and two beautiful grandchildren, who give me all the help I need and great joy and purpose. My faith in God never fails me, and helps me keep going with hope. I've also honed my sense of humor. I carry a page of jokes with me at all times and regularly e-mail friends across the country with "My Sunday Bulletin," a compendium of jokes I collect from my e-mail friends. My motto is "Can't Walk or Talk But Can Always Laugh."
ALS Links.com Internet Portal For The ALS Community. A Internet portal for the amyotrophic lateral sclerosis community. Includes the ALS Digest in web format for easy navigation with archives and search engine. http://www.alslinks.com
Extractions: var WebSiteBaseURL = "http://www.lef.org/protocols/prtcl-008.shtml" translation by SYSTRAN MEMBERSHIP PRODUCTS MAGAZINE ... CHECKOUT Health Concerns Selector Select Health Concern Acetaminophen (tylenol) Poi... Acne Adrenal Disease Age-associated Mental Impai... Alcohol Induced Hangover: P... Allergies Alzheimer's Disease Amnesia Amyotrophic Lateral Scleros... Anemia-thrombocytopenia-leu... Anesthesia And Surgical Pre... Anxiety And Stress Arrhythmia (cardiac) Arthritis Asthma Atherosclerosis Attention Deficit Disorder ... Autism Autoimmune Diseases Avoiding Vitamin - A Toxicity Bacterial Infections Balding Bell's Palsy Bladder Conditions Breast Cancer Bursitis Cancer - Overview Cancer Adjuvant Treatment Cancer Chemotherapy Cancer Clinics Cancer Gene Therapy Cancer Prevention Cancer Radiation Therapy Cancer Supplements Cancer Surgery Cancer Treatment: The Criti... Cancer Vaccines Candida (fungal, Yeast) Inf... Cardiovascular Disease: Co... Cardiovascular Disease: Ove... Carpal Tunnel Syndrome Catabolic Wasting Cataract Cerebral Vascular Disease Cervical Dysplasia Cholesterol Reduction Chronic Fatigue Syndrome (cfs) Cirrhosis Colitis (ulcerative) Colorectal Cancer Common Cold Congestive Heart Failure An...
ALS And Associated Web Sites Links to sites about amyotrophic lateral sclerosis including chat rooms and message boards. http://www.geocities.com/sweekes99/ALStitle.html
Amyotrophic Lateral Sclerosis / Family Village Library Library A B. amyotrophic lateral sclerosis. ALS Discuss A forum to discuss amyotrophic lateral sclerosis (Lou Gehrig s Disease). http://www.familyvillage.wisc.edu/lib_als.htm
Extractions: Web: http://www.alsa.org/ The ALS Association seeks to promote awareness and understanding of ALS and the work of The ALS Association by providing up-to-date information and education materials to the ALS community ALS patients and families, caregivers, researchers and members in the health care fields. The ALSA website is another component in the delivery of information specific to ALS. Our purpose is to provide accurate and timely information as well as a resource directory pointing to sources of information. ALS Informer This list was created to permit the exchange of information between persons with ALS, family members of PALS, caregivers, researchers, or anyone interested in finding out more about this horrible disease. The sharing of information is to create awareness, provoke thought, and stimulate research about amyotrophic lateral sclerosis (ALS) or Lou Gehrigs disease. ALS Discuss
Welcome To The Angel Fund Dedicated to increasing awareness of amyotrophic lateral sclerosis (ALS) and based at Massachusetts General Hospital. http://www.theangelfund.org
Extractions: The Angel Fund recently held its 4th annual Dinner and Silent Auction at the Boston Park Plaza Hotel, an event that raised over $135,000 for ALS (Amyotrophic Lateral Sclerosis) research at the Cecil B. Day Neuromuscular Research Lab at Massachusetts General Hospital. Among those who were instrumental in the success of the event and the three-day international research symposium that preceded the event were (from left) Richard P. Kennedy, President of the Angel Fund; Dr. Robert H. Brown, Jr., Director of the Cecil B. Day Neuromuscular Research Center at Mass General; Janice Nigro, Angel Fund Director and symposium coordinator; and Eugene Nigro, Founding Director of the Angel Fund. Words of Inspiration
Extractions: Amyotrophic lateral sclerosis (also called ALS or "Lou Gehrig's disease") is a classic motor neuron disease. Motor neuron diseases are progressive chronic diseases of the nerves that come from the spinal cord responsible for supplying electrical stimulation to the muscles. This stimulation is necessary for the movement of body parts. ALS is progressive and fatal. The usual causes of death of patients with motor neuron diseases are not directly related to the disease, but result from simultaneous additional illnesses which ultimately occur because of weakness of the body. These illnesses are often infections. ALS occurs most often in adults in the fifth through seventh decades of life. It progressively leads to death in 2 to 7 years. The cause is unknown.
Amyotrophic Lateral Sclerosis amyotrophic lateral sclerosis (ALS). Overview. Ross MA. Toward earlier diagnosis of amyotrophic lateral sclerosis revised criteria. rhCNTF ALS Study Group. http://neuroland.com/deg/als.htm
Extractions: Neuro Med Amyotrophic Lateral Sclerosis (ALS) Overview Also known as: Motor neuron disease, Lou Gehrig's disease a number of overlapping syndromes such as pseudobulbar palsy, progressive bulbar palsy, progressive muscular atrophy and primary lateral sclerosis. Annual incidence is approximately 1/100,000 population Pockets of high incidence in Guam (ALS-Parkinson-dementia complex), the Kii peninsula of Japan, and western New Guinea. 95% of cases in the US are of the sporadic variety, but a few families have several members with the typical clinical picture of sporadic ALS arising in an autosomal dominant pattern. Onset of the disease can be as early as the third decade of life, most cases begin after age 40, and the incidence increases into the eighth decade. Etiology: unknown Male = Female Symptoms Slowly progressive muscle weakness involving the limbs, trunk, respiratory muscles, throat, and tongue. Onset is insidious, and initial symptoms may be confined to a single limb, especially the distal muscles.
ALS Center At MCP Hahnemann University The ALS Center of MCP Hahnemann University, Philadelphia, PA, provides compassionate,complete, multidisciplinary, state of the art care and access to the newest, most promising clinical trials in amyotrophic lateral sclerosis ALS, muscular dystrophy MD and neuromuscular disease. http://www.mcphu.edu/medschool/depts/neurology/alsctr/alshome.htm
Taylor & Francis Group - Publication amyotrophic lateral sclerosis amyotrophic lateral sclerosis. amyotrophic lateral sclerosis Association of America www.alsa.org; Center for Neurologic Study www.cnsonline.org; http://taylorandfrancis.metapress.com/openurl.asp?genre=journal&issn=1466-0822
Index The personal story of Warren Lee Stickney, who had amyotrophic lateral sclerosis. Also links for further reading. http://www.geocities.com/HotSprings/4340
Extractions: View Page 1 Guestbook PICTURESQUE PALS P eople with A myotrophic L ateral S clerosis Honoring PALS Everywhere My dad with some of his grandchildren,1998. My dear father, Warren Lee Stickney, lost his battle with ALS on January 16, 1999. I wanted to do something to honor his memory and to celebrate his life, so I thought of dedicating a web page to him. Then I deceided that there were far too many PALS in this world who have loved ones that would like to do the same, so this page is dedicated to all PALS everywhere. If you have a story and/or pictures of a PALS you would like to honor please e-mail me at wlsals@yahoo.com ALS(also known as Lou Gehrig's Disease) is a neurological disease affecting the nerves that supply all voluntary muscles. It is one of the most devastating diseases there is. There is no cure. ALS affects the muscles of the arms, legs, face, tongue, speech, swallowing and breathing- eventually leading to paralysis. ALS does not affect thinking or intelligence. Feb. 1999 - This is my story of my dad, I will just write what I am thinking at the time so I may sound like I am rambling but please forgive me. I just want people to know what kind of person the world has lost. I have heard it said that PALS are the nicest people you could ever meet and this was true of my dad. A little about him. Warren Lee Stickney was born in June 1932, he was the youngest of several children. Grandpa (I started calling him Grandpa almost 20 years ago when my nephew Daniel was born) used to always tell us kids of his adventures as a child (and I am still lucky enough to have his older brother, Bert, come and visit and tell these tales to me and my kids). Grandpa grew up in Michigan and lived on the lake. He spent his boyhood camping, fishing, swimming,etc.
Amyotrophic Lateral Sclerosis: A Challenge For Speech-Language Pathology amyotrophic lateral sclerosis. A Challenge for SpeechLanguage Pathology By Pamela Mathy. amyotrophic lateral sclerosis. Seminars in Neurology, 18 (1), 27-39. http://www.asha.org/public/speech/disorders/als-amyotrophic-Lateral-Sclerosis.ht
Extractions: @import url( /styles/importmenuP.css ); Skip to: content navigation Our site's pages are optimized for Web browsing software that supports current Web standards, as established by the World Wide Web Consortium (http://www.w3c.org/) . Content is accessible from older or less standards-compliant technologies, but its presentation will not be identical to visitors with standards-compliant software. Read more on our site's changes and accessiblity. My Account Find a Professional Shop Logged in as: Guest Login Search for: ADVANCED SEARCH Home For the Public Speech Language and Swallowing ... Disorders and Diseases A Challenge for Speech-Language Pathology By Pamela Mathy A myotrophic Lateral Sclerosis (ALS), first identified in 1869 by the French neurologist, Jean-Martin Charcot, is a relentlessly progressive degenerative motor neuron disease that primarily affects the motor neurons of the brain and spinal cord. Lou Gehrig, with whom the disease is often associated, brought international attention to ALS in 1939, when it caused him to retire from baseball. More recently, a variety of public figures from actors (Michael Zaslow) to physicists (Stephen W. Hawking) to retired university professors interviewed on Nightline (Morrie Schwartz) to senators (Jacob Javits) have focused attention on this-devastating disease. Symptoms The early symptoms of ALS are varied. For some it begins with speech slurring, difficulties with swallowing, and/or hoarseness. Others may experience uncharacteristic clumsiness or tripping. Difficulty lifting may be the initial symptom for others. Clinically, the signs and symptoms are divided into two areas-spinal functions and bulbar functions. Three-quarters of people report initial spinal symptoms (weakness in the upper and/or lower extremities) and about one-quarter present with bulbar symptoms (weakness with changes in both speech and swallowing). Both upper and lower motor neurons characteristically become involved as the disease progresses.