Donate to the cause here: www.movementforhope.org Website: www.movementforhope.org Film and Audio Amber M. Hill, Bhaskar Muppana, Robert Evenden Director: Amber M. Hill Film Editor: Robert Evenden Featured dancer: Aviva Stoch, Sarah's Daughter (14 years old) - dance choreographed for her mother Special thanks to the University College London Slade School of Fine Arts Movement for Hope: Our mission is to encourage the advancement of art and science, unified by movement, to raise awareness for neurological diseases and multimedia art. Move Hope Project: This video features one of two diseases we are campaigning for in the Move Hope Project, MND. Motor Neurone Disease, also known as Amyotrophic Lateral Sclerosis and Lou Gehrig's Disease, is characteriszed by a inexorable degeneration of alpha motor neurons in the ventral horn of the spinal cord and brain stem (lower motor neurones) and of the motor neurones in the motor cortex of the brain (upper motor neurones) It progressively weakens the muscles to the point of wasting of skeletal muscles due to motor neurone involvement. It eventually takes away the ability to walk, eat, speak, and breathe. About 90-95% of MND cases are sporadic and only 5-10% genetic. The life expectancy is usually 2-5 years, but Sarah has beat the odds for nearly 12 years now (diagnosed in 2000)! She is an exceptional woman with a genuinely positive attitude and spirit of giving. please consider donating Facebook: www.facebook.com Twitter <b>...</b>

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At Johns Hopkins, researchers and doctors are working together to explore the impact of stem technology on ALS. The Robert Packard Center for ALS Research at Johns Hopkins has helped uncover new genes for familial ALS, researched nerve repair, worked actively on genetic risk factors, developed a variety of animal models for testing therapies, explored ALS biology, advanced stem cell therapy, and researched ways to counter muscle atrophy.

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Amyotrophic Lateral Sclerosis (Lou Gehrig's Disease

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Amyotrophic Lateral Sclerosis | ALS at UAMS

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Richard Smith is director of The Center for Neurologic Study (CNS), principal investigator at Coordinated Clinical Research and member of the honorary medical staff at Scripps Memorial Hospital, La Jolla, CA. He is also consultant at Isis Pharmaceutical Corporation and Eli Lily. As well, he is coauthor of the books: Interferon Treatment of Neurologic Disorders and Handbook of Amyotrophic Lateral Sclerosis. Smith holds a BS from Brandeis University and a MD from the University of Miami. Produced by New Media | UFM www.newmedia.ufm.edu http

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Hi again. I'm Jeannie aged 30, I first noticed ALS/MND in June 2000, diagnosed with ALS July 2001...this video is to show everyone how ALS affects you. I thought I'd make another video of me walking so you can see how I'm doing.

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Dr. Stan Appel, Director MDA/ALS Center at Methodist Neurological Institute in Houston, speaks about cognitive and behavioral changes in patients with ALS, amyotrophic lateral sclerosis or Lou Gehrig's disease.

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Amyotrophic lateral sclerosis (ALS), often called as "Lou Gehrig's Disease," is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. It is a form of motor neuron disease.

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North American investigators led by Dr. Rosa Rademakers, Ph.D. and other neuroscientists at Mayo Clinic in Florida have found a genetic abnormality they say is the most common cause of two different but related forms of neurodegenerative disease — frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease.

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My friend Kurt also has als and this video was sent to friends via email so we could all see how he's doing. Kurt was dxed 10 yrs ago but had symptoms 3 yrs prior.

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My Father with my son, special moments in hard time in our lives.The most important thing is be together and always trust in God- Because we believe in miracle.

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My Father, Don Anderson, died in 2010 from Amyotrophic lateral sclerosis (ALS) I made this video to show how awful his life was before he died. Recently in 2011 scientists discovered the cause of ALS but there is much more that we need to know for a cure It is a terrible disease and always fatal

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How I recovered from a terminal illness - Amyotrophic Lateral Sclerosis.

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Im Jeannie aged 29, I first noticed ALS/MND in June 2000, diagnosed with ALS July 2001...this video is to show everyone how ALS affects you.

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MDA's ALS Division Co-Chairperson and MDA National Vice President Augie Nieto was featured during hour three of the 2011 MDA Telethon. Augie, a prominent leader in the nation's fitness industry for nearly three decades, received a diagnosis of amyotrophic lateral sclerosis (ALS, or Lou Gehrig's disease) in March 2005. Augie approaches his role as co-chair of MDA's ALS Division with the same ironclad will and determination that catapulted him to entrepreneurial heights in the fitness world. To learn more about Augie, or how you can support "Augie's Quest," please visit augiesquest.org.

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On Friday, November 4, 2011, the ALS Society of Manitoba held its 6th Annual Conference on ALS at Canad Inns Polo Park, Winnipeg. The event was attended by health care professionals, as well as ALS clients, their families and caregivers. The nearly 100 attendees were treated to a continental breakfast and a buffet lunch, as well as learning about what has been happening in ALS research and about what it is like to live with and care for someone living with Amyotrophic Lateral Sclerosis. Guest speakers included Denise Figlewicz Ph.D, Dr. Colleen O'Connell MD FRCPC, Fred Nelson MSW RSW and a person living with ALS. There were also displays relating to health care support set up in the foyer. Thank you to everyone who made this event possible. We look forward to seeing you all again next year.

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The underlying disease process of amyotrophic lateral sclerosis (ALS and Lou Gehrig's disease), a fatal neurodegenerative disease that paralyzes its victims, has long eluded scientists and prevented development of effective therapies. Scientists weren't even sure all its forms actually converged into a common disease process. But a new Northwestern Medicine study for the first time has identified a common cause of all forms of ALS. Read more at Futurity: www.futurity.org

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Go to www.ericiswinning.com for more information on ALS. This is a trailer to a documentary on people who have slowed and even stopped the progression of their ALS.

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We have fun too you know, there are some perks of having als lol

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A documentary about life with Amyotrophic lateral sclerosis

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MDA Vice President of Research Sanjay Bidichandani, MBBS, Ph.D., explains the significance of new ALS research that has identified a "repeat expansion" mutation as the most common known genetic cause of familial ALS. The mutation also accounts for some cases of sporadic ALS. (For more on this finding, see C9ORF72 Mutation Most Common Cause of ALS, FTD. alsn.mda.org

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Video Project for Anatomy about ALS

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By Zacharias Vamvakousis. A free and open source project. More info: theeyeharp.blogspot.com The main goal of the EyeHarp project is to allow people with paralysis resulting from Amyotrophic Lateral Sclerosis to play music using only their eyes. To build this, I was inspired by the EyeWriter open source initiative: "...a low-cost eye-tracking apparatus & custom software that allows graffiti writers and artists with paralysis resulting from Amyotrophic lateral sclerosis to draw using only their eyes". (www.eyewriter.org) Alternatively, the instrument can be controlled using the mouse pointer (MouseHarp version). Then the free software camera mouse (http can be used to control the instrument with head movements. Any technology that can take control of the mouse pointer can be used in order to control the instrument. That way the mouseHarp could be an appropriate instrument for many cases of people with physical disabilities. The mouseHarp version is completely independent from the eyeWriter project. Combining the mouseHarp source with the source of the eyeWriter project, we get the eyeHarp! A low-cost gaze controlled musical instrument! Both versions are free and open source. The main contribution of this project is the design of an appropriate interface to play music using any eye tracing device. In order to evaluate the interface, a low-cost eye tracking device was constructed using the instructions of the EyeWriter Project. I am grateful to the EyeWriter team. Without <b>...</b>

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Recently published studies by a researcher in the Faculty of Medicine & Dentistry demonstrate that ALS -- known as Lou Gehrig's disease -- damages neurons in parts of the brain responsible for cognition and behaviour. ALS, which stands for amyotrophic lateral sclerosis, is a fatal neurodegenerative disease that eventually leaves patients unable to move, breathe or swallow. Previous research has shown about 50 per cent of patients with ALS also have mild cognitive and behavioural changes, but between five and 15 per cent of patients can have severe changes resulting in dementia. In Canada, between 2500 and 3000 people live with the disease. Most die within two to five years of diagnosis. Sanjay Kalra, a researcher in the faculty's Division of Neurology and a practising neurologist, has published two papers this year in the American Journal of Neuroradiology providing evidence that ALS affects more than just the motor cortex, the part of the brain responsible for motor function.

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Episode 33 : "Variety of Awareness" — In 30 days the community hosted three Often Awesome benefit shows in order to help spread awareness and help share Tim's message of how this is America's best kept secret disease. Scott Avett of The Avett Brothers intros this episode. Often Awesome The Series is a web series about Tim and Kaylan's battle with ALS (Lou Gehrig's Disease). Its a story about love, friends, strength and courage. Join us every month for a new chapter in this amazing adventure. For more information about Tim and Kaylan's fight and to help them please visit : oftenawesome.org Do you want to help support this series? Info here allacesmedia.com Often Awesome The Series on Facebook: facebook.com Often Awesome The Series Website: oftenawesome.com For more information about the filmmakers visit allacesmedia.com

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My attempt to raise awareness on the dreadful disease that is Amyotrophic Lateral Sclerosis (ALS), otherwise known as Lou Gehrig's Disease.

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Now is the time to put your muscle, your strength and your commitment behind MDA. Be the next to flex, the next to join in the fight. Make a Muscle, Make a Difference! Be sure to tune in for an all-new Telethon experience!

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Episode 32 : "A Day in the Life" — This episode focuses on the daily routine that Tim lives with. The care that he receives from his wife, friends and nurses. If you ever wanted to know what living with ALS is...this is the one episode to watch. Often Awesome The Series is a web series about Tim and Kaylan's battle with ALS (Lou Gehrig's Disease). Its a story about love, friends, strength and courage. Join us every month for a new chapter in this amazing adventure. For more information about Tim and Kaylan's fight and to help them please visit : oftenawesome.org Do you want to help support this series? Info here allacesmedia.com Often Awesome The Series on Facebook: facebook.com Often Awesome The Series Website: oftenawesome.com For more information about the filmmakers visit allacesmedia.com

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Doug spoke to his teammates after a day of racing and a special Sport Systems MountainTop Cycling organization recognition. This clip was captured after the 2011 Sandia Peak MTB Championship race, during our profiling Champion New Mexico Mountain Bike Racer Doug Schneebeck. Part of theView-Trend* More Than Digital Multimedia contribution to the Knight Wilder ALS Documentary Compilation. another View-Trend More Than Digital Multimedia production **Any and all of the audio and video including musical selections or edited multimedia clips content used or included in this video are used here under the fair-use provisions of the copyright.** Produced by Glynn David Harris using HP Computers, Sony Vegas Pro and the Adobe Creative Suite for a View-Trend* More Than Digital Multimedia client. To make a Tax Deductible donation or, for More Information: Please visit the Oso High Endurance Sports web site: www.osohigh.com and Sport Systems MountainTop Cycling www.mountaintopcycling.com To request all or part of this or related program event clips from the associated View-Trend* Cinematic Stock Footage Archives or, for on-location video production assignment pricing and availability for your upcoming event, email your request with your contact info to: viewtrend.mtd@gmail.com

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(Part 5 of 8) Martin Marsala MD spoke at the "Spotlight on Disease Team Awards: ALS," an educational event presented at the CIRM Governing Board meeting on June 23, 2010. Marsala is a professor of anesthesiology in UC San Diego School of Medicine. To view the other videos in this playlists, go to: www.youtube.com

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Public Service announcement about Amyotrophic Lateral Sclerosis.

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(Part 4 of 8) Mark Bonyhadi, Ph.D. spoke at the "Spotlight on Disease Team Awards: ALS," an educational event presented at the CIRM Governing Board meeting on June 23, 2010. Bonyhadi is director of clinical business development for cell therapy in the Cell Therapy Systems group at Invitrogen, part of Life Technologies. To view the other videos in this playlists, go to: www.youtube.com

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(Part 1 of 8) Robert Klein, JD and Larry Goldstein, Ph.D. spoke at the "Spotlight on Disease Team Awards: ALS," an educational event presented at the CIRM Governing Board meeting on June 23, 2010. Klein and Goldstein introduced the CIRM ALS Disease Team. Klein is chair of the CIRM Governing Board. Goldstein is the principle investigator of the CIRM ALS Disease Team and director of the UC San Diego Stem Cell Program. He is also a Howard Hughes Medical Institute investigator and professor in the department of Cellular & Molecular Medicine in the UC San Diego School of Medicine. To view the other videos in this playlists, go to: www.youtube.com

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(Part 3 of 8) Don Cleveland, Ph.D. spoke at the "Spotlight on Disease Team Awards: ALS," an educational event presented at the CIRM Governing Board meeting on June 23, 2010. Goldstein is a co-principle investigator of the CIRM ALS Disease Team and member of The Ludwig Institute. He is also chair of the department of Cellular and Molecular Medicine at the UC San Diego School of Medicine. Cleveland was introduced by Larry Goldstein, Ph.D. To view the other videos in this playlists, go to: www.youtube.com

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