VECTTOR has not yet been cleared by the FDA For more information please visit 2STIM.com or call (361) 992-9433.
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BrainPOP's beloved animated duo, Tim and Moby, present the topic of Duchenne in this short, animated movie. Produced in partnership with Parent Project Muscular Dystrophy, this four minute video strives to provide kids of all ages with a clear understanding of Duchenne.
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This story documents Ryan Benton's most recent trip from his home in Wichita, Kansas to the Stem Cell Institute in Panama City, Panama to receive stem cell therapy for muscular dystrophy. Follow Ryan as he lands at Tocumen International airport, receives treatment and returns home. Listen to interviews from Ryan, his family and friends after his return home.
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As an 8-year-old boy becomes the first US gene therapy patient for muscular dystrophy, one of the researchers behind the therapy talks about the 20 years it took to get there, and what lies in the future. Watch this ScienCentral video for more. www.sciencentral.com
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Researchers have discovered a potential drug for the most common kind of muscular dystrophy and they're using a protein already found in the human body to combat muscle damage. www.sciencentral.com
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Dr. Maurice Swanson talks about what muscular dystrophy is and how it affects the body.
Bryan Arnold of Anchorage, Alaska, educates people about his degenerative disease, Duchenne muscular dystrophy (DMD). During his junior year of high school, he produced this movie about living with DMD. It is now shown in schools statewide and Bryan hopes to extend his advocacy reach beyond Alaska to the rest of the country. Because of his work, Bryan received a 2009 Yes I Can! Award (self-advocacy category) from the Council for Exceptional Children. The award was presented to him on April 3 at the CEC 2009 Convention & Expo in Seattle.
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This short documentary on Muscular Dystrophy takes a look at how people that have this rare and mysterious disease live with it and all they have is hope as there is no cure. Please comment on the video to show your support. Produced by Michael Kaneff. www.Kaneffprods.com and MDA.
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Limb-Girdle Muscular Dystrophy 2A individual displaying the course of muscular dystrophy through the activity of rolling over in b Limb-Girdle Muscular Dystrophy 2A individual displaying the course of muscular dystrophy through the activity of climbing the stairs in April 2008. To learn more about LGMD2A mobility visit www.beyondlabelslimitations.com
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Duchenne Muscular Dystrophy is a deadly disease . For more information watch the video .
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In the PSA, called "Have You Seen This Boy," Ms. Dukakis helps visitors understand the initial symptoms of Duchenne "If you see a boy who struggles to walk or climb stairs, who has enlarged calves, who pulls himself up in a different way and can't seem to keep up with his peers, you could be noticing symptoms of Duchenne muscular dystrophy."
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Steve Dale interviews Joe Kornegay, DVM, PhD, DACVIM (Neurology) at the 2009 ACVIM Forum & Canadian VMA Convention in Montreal. For the past 25 years, Dr. Kornegay has studied a spontaneous canine disease termed golden retriever muscular dystrophy (GRMD), which serves as an animal model for Duchenne muscular dystrophy (DMD) of humans. Both conditions are X-linked, occurring due to mutations in the dystrophin gene. His research group has defined key clinical and pathologic features of GRMD to both better understand disease pathogenesis and to also utilize these parameters in assessing treatment efficacy. In recent years, working with collaborators, Dr. Kornegay and his colleagues have studied various treatments (cell, molecular, and pharmacologic approaches) in affected dogs. Results of these preclinical studies should guide use of similar treatment strategies in DMD patients. For more information, please visit www.ACVIM.org.
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Meet Aidan, a cheeky, happy and typical 6 year old boy (7 in August) who is living with Duchenne Muscular Dystrophy, a cruel and unforgiving muscle wasting disease that will cut short his life if a treatment does not come in time. Like 35% of cases, Aidan DID NOT inherit DMD, it is his body's own spontaneous mutation, meaning there will always be boys born with Duchenne. Please watch his video and help us end Duchenne. ********************************************************************************************************************** Aidan could be described as your typical six year old boy. He's in to all manner of critters and creepy crawlies, slugs and bugs, but his absloute favourites are all things slimy...yuck! He loves riding his bike and his scooter when his energy levels permit, and is best mates with hi younger brother, Owen. He adores his baby brother, Ethan, who was born in November 2009, and helps care for him in every possible way. He is a popular member of his class at school, where he excels at reading, mathematics, art and computers. He spends his playtimes doing his best to keep up with his friends on his mobility scooter, playing on the adventure playground, and rugby with his mates - who always make sure Aidan gets a kick! If he is too tired to play, he makes his way over to the Special Needs Unit where he plays computer games, or selects a dvd and a big beanbag and will "chillax" until playtime is over. When he is full of energy he spends his <b>...</b>
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Help stop the chaos and destruction caused by the Steve Way. Donate to the Muscular Dystrophy Association and help find a cure.
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see www.cellmedicine.com
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A regular stretching regime to keep muscles and tendons supple should be part of a young man's daily routine in order to help prevent the development of contractures. Contractures are a tightening of the muscle and tendons, which limit the full range of movement in a joint. They are inevitable if a regular stretching program is not part of a boy's daily regime. This tightness occurs because not all muscles lose strength at the same time or pace, and boys with DMD develop irregular postures to compensate for this uneven weakness. This CD walks you through different types of stretches for DMD. To obtain a copy of our stretching cd, please visit www.parentprojectmd.org Contact information can be found at the bottom of the page. www.parentprojectmd.org www.duchenneconnect.org
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Reflex Sympathetic Dystrophy (RSD) is a chronic, painful, and progressive neurological condition that affects skin, muscles, joints, and bones. For more information on this disorder, please visit www.rsds.org
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This presentation is still true of many boys and youths affected by Duchenne around the world. Through improved treatment, many of our youths and men are living into their 20's and 30's. Parent Projects worldwide have played a large part in improving longevity and quality of life, but more research is needed to test many viable treatments to preserve muscle strength. Parent Project Australia is now known as Duchenne Foundation or TheBlueBall but we'll always be a member of United Parent Projects Muscular Dystrophy.
www.nucleusinc.com This 3D medical animation describes how this chronic condition causes persistent burning, swelling, and pain in one or more of your limbs. This animation compares the normal inflammation response to the abnormal response that is caused by CRPS/RSD.
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We can all help raise awareness for this devastating degenerating muscular problem by passing this video on. Duchenne Muscular Dystrophy is a terminal, non curable disorder that affects mainly boys. Will you help?
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NOTE: Check out the 1 Year Journey Video also. This is 22 year old Todd Harrison's Becker Muscular Dystrophy VECTTOR treatment progress...Find us on facebook also @ Defying Muscular Dystrophy
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VECTTOR has not yet been cleared by the FDA A patient discusses his success with Dr. Donald Rhodes' VECTTOR treatment to improve walking and balance in Becker Muscular Dystrophy. For more information visit on South Texas Innovative Medicine visit 2STIM.com or call (361) 992-9433.
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Short documentary on Muscular Dystrophy on how children with the rare disease, Muscular Dystrophy, go to summer camp each year and interact with others who have the same disease. Produced by Mike Kaneff. www.Kaneffprods.com
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Limb-Girdle Muscular Dystrophy 2A individual displaying the course of muscular dystrophy through the activity of rolling over in bed in April 2008. To learn more about LGMD2A mobility visit www.beyondlabelslimitations.com
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www.medra.com - Breakthrough Stem Cell Treatment for Muscular Dystrophy.
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This is my one year journey of defeating Becker Muscular Dystrophy with the VECTTOR treatment. How is it possible to regain strength with MD? VECTTOR is the answer just watch!
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This video guides you for treatment through yoga, ayurveda, acupressure and domestic remedies for diseases like Cerebral Palsy, Muscular Dystrophy, Mongolism, Multiple Sclerosis and Thalassemia. Click www.rajshri.com to watch more Baba Ramdev Videos
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A short documentary on Muscular Dystrophy and the people with the disease. Produced by:Michael Kaneff when I was 17 years old. www.Kaneffprods.com
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Short Video about the people who live with the rare disease, Muscular Dystrophy, and how it sadly affects their everyday life. The 2009 MD Video link is www.youtube.com and the most recent 2010 Video link is www.youtube.com Produced By Mike Kaneff. www.Kaneffprods.com
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