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Fighting Duchenne Muscular Dystrophy: Dr. Benjy Seckler at TEDxBerkshires 

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Charley's Fund is named for Tracy and Benjy Seckler's son, Charley, who, to the casual observer, is simply a quirky little kid with irresistible curls and a mischievous sense of humor. Charley's devilish smile belies what is going on inside his body, for his muscles are deteriorating at an alarming pace. Unless a cure or treatment for Duchenne Muscular Dystrophy is found, Charley will lose his ability to walk by adolescence, and subsequently lose all muscle function. Like all boys with Duchenne, he will die from respiratory or heart failure in his late teens or early twenties. Charley's Fund was incorporated four months after the diagnosis. By refusing to surrender, the Seckler's turned a basic assumption on its head -- that the most complicated problems require a phd or an expert to come up with solutions. Their experience teaches us that in fact, it is determination and innovation that can drive toward a solution. And that determination and innovation can come from anyone.
In the spirit of ideas worth spreading, TEDx is a program of local, self-organized events that bring people together to share a TED-like experience. At a TEDx event, TEDTalks video and live speakers combine to spark deep discussion and connection in a small group. These local, self-organized events are branded TEDx, where x = independently organized TED event. The TED Conference provides general guidance for the TEDx program, but individual TEDx events are self-organized.* (*Subject to certain rules and regulations)

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6 июн 2024

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Комментарии : 13   
@MrJpm1989
@MrJpm1989 3 года назад
Today December 5th would have been my son's birthday but in 2009 he passed away from Duchenne Muscular dystrophy. My son Johnny was 19 years old when he died. A cure must be found for these wonderful sons and daughters. God bless everyone 🖤
@carinebejjani
@carinebejjani 10 лет назад
My brother has DMD he is turning 31 on March 1st. I relate to everything you said and salut your hope.
@TaraAGM
@TaraAGM 10 лет назад
Incredible. What a great way to approach improving research and treatment. I will be looking into Charlie's Fund.
@Ramcio1975
@Ramcio1975 10 лет назад
I am 38 years old and AND HAVE "Duchenne Muscular Dystrophy (DMD)".
@lisauncles6075
@lisauncles6075 3 года назад
Please my 17 year old son really needs help....he's healthy as far a DMD goes.....if there is support we'll be happy to get involved
@Barmorris
@Barmorris 10 лет назад
Dr. Benjy is a real hero
@mihaelnet
@mihaelnet 9 лет назад
Hi Ramcio1975, can you contact me about DMD? My wife's brother have DMD and we fight with this horrible diesiese, he is now 19 and on ventilation system.. Thanks
@mazenerksousi1596
@mazenerksousi1596 3 года назад
Exercise is useful and muscles will excrete protein. Please all families of patients who exercise and the patient will improve without any treatment or medication
@praveenjairam5887
@praveenjairam5887 6 лет назад
But still we don't have proper cure for the disease.I am waiting for the treatment.
@donniejon7961
@donniejon7961 4 года назад
I like ted talks
@frankkara7240
@frankkara7240 3 года назад
Is muscle dystrophy can cure ?
@meharkhatoon3038
@meharkhatoon3038 Год назад
no
@damianculhane
@damianculhane 10 лет назад
great work guys...keep raising the profile of DMD!!
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