hypertrophic cardiomyopathy youtube video

<iframe allowfullscreen="" frameborder="0" height="315" src="http://www.youtube.com/embed/tmlTHfVaU9o" width="420"></iframe>


<iframe allowfullscreen="" frameborder="0" height="315" src="http://www.youtube.com/embed/a4LSEXsvRAI" width="420"></iframe></div>

Austin, Texas teen Ben Breedlove, who died Christmas Day, this video touches on the left behind the health problems of your life - a video gone viral on YouTube.Bere has been growing year on YouTube, dating from their date of birth of children, wit and wisdom of man, now 18 years that have passed his SATs to get more advice than that.But before Christmas, Ben made a different type of video, funny - but also very sad. Ben's life in danger in the world to share their personal struggles with heart disease, and asked how is your life every day.Ben was viewed more than a million video views YouTube, CBS 'Anna Werner reports.Deanne Breedlove, Ben's mother, told CBS News, "was made 13 months ago. We were under a cardiologist, and some tests and found to have a condition called hypertrophic cardiomyopathy."Hypertrophic cardiomyopathy, the heart muscle of the heart pump blood more difficult - and chest pain, hypertension, and ultimately cause heart failure. His YouTube video, Ben in detail how "cheated death" three times, four of age and again at the beginning of this month before the paramedics revived her school.Ally Breedlove, Ben's sister, said, "I found him to our home port, and is happy just sitting alone and asked him if he woke and said:" I think. "And he, therefore, happy to be back in our family, he said, but he did not want to just be back in this room."Shortly afterwards, Ben, who had returned to peace. He died on Christmas yard, playing with his younger brother. His family did not see the video until the next day. Christmas was his last gift to them."I'm very proud of him and decided to share with you something that it was weak and, therefore, be personal," says Deanne Breedlove.Ben and his followers and the world with a message of hope.And, at least, it seems that YouTube, the world's last

Hypertrophic Cardiomyopathy Association and a draft law to help prevent sudden cardiac arrest (SCA) in children and adolescents

Last year, a meeting between Salberg a chance to Lisa, Founder and Executive Director of the Association of cardiac hypertrophic (HCMA), and Congressman Frank Pallone, Jr., (Dem., NJ) a key role in the drafting of heart health education and awareness, risk assessment, and training in schools (hearts) , introduced a bill to Congress today a balloon.Call the awareness of sudden cardiac arrest is one of the main pillars of the HCMA, and national resources for patients with cardiac hypertrophic (HCM), and the most common genetic disease of the heart. HCM, which results in a thickening of the heart muscle is the main cause of sudden cardiac arrest (SCA) in children and young adults.Hearts of the Act states SCA awareness in schools and child care centers and requires preventive measures best to save the lives of young people. It requires the Minister of Health and Human Services to coordinate with the Centers for Disease Control and patient advocacy and health organizations and professional development and distribution of materials for Supply Commodities Authority. It also requires guidelines on the development of defibrillators automated external saving lives in schools and information on cardiopulmonary resuscitation (CPR) training.In the United States there are 600,000 people with HCM, and there are nearly a million of other genetic diseases that can cause in the form of goods ration of young people. With a better knowledge of the warning signs and symptoms of heart disease in young people, can save thousands of lives every year."Most people find their way to me and the HCMA too late to save the life of a family member," said Salberg. "Most tragically when I pity the parents who lost children and adolescents healthy.""Pleased HCMA that have been submitted to the law of Hearts to help ensure that families have the opportunity to get treatment for HCM and other causes of the commodities in the young, and if we save one person from suffering cardiac arrest and its aftermath, this legislation pays for itself within a year."On hypertrophic cardiomyopathy Association (HCMA)Founded in 1996 by Lisa Salberg, and HCMA is a non-profit 501 (c) (3) organization that provides comprehensive information on hypertrophic cardiomyopathy (HCM), a hereditary disease that causes thickening of the heart muscle. And HCMA provides support and advocacy for patients with HCM and their families and medical providers to help prevent premature death and to enhance understanding of the world about this crippling disease