Blaise talks to Oprah About Prader Willi Syndrome
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thnx for sharing.
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@renaycompere unfortuantly, at what cost.
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I am doing a report for one of my elementary education classes, and I would like to be able to put this video in my ppt. Can you forward this video to me so that I may add it to my presentation. I thought that it was a really cute video and I would like to educate my classmates through first hand experience. Thank you.
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I love this video. Of course there are things that can help. There are treatments and medications, that will eventually be discovered that will end the hunger. Researchers around the world are working on developing things that will not only help those living with PWS but also people who struggle with obesity. Keep going mom! This is awesome.
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@ArtemisMS I don't think anything can help this guys, maybe in the intrauterine life?
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@choforito4000 stem cell research can perhaps one day help
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This is a GENETIC condition, sadly there's no cure... you can't change the genetic information.
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my 14 week old grandson has pws. I pray all the time for God to heal him. You are a sweetiepie Blaise! All my love and prayers go out to you and your family!
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@kitihoku Hey I have it to but i have type 1 though im a girl and my name is Jessica and im 14 years old and struggle with pws each day. just keep your preciouse angle healthy so he would not be in my place right now that i weigh 265.4 pounds my family and i need help to keep the food lock up all the time but they just can't do it alone i need help. please.
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I knew that they were always hungry my sister had PWS but for some reason this was like a big SLAP in the face. Maybe because its a child holding this sign that makes it more sad. Because when my sister was a child I was too, and helping my mom, so it was natural for me, I pray for Blaise as well as all the others out there with PWS
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What a cute kid. Thanks for the video. All the best to Blaise and his parents. I hope a remedy is found for this problem, and Blaise can live a normal life.
doughtyone 2 years ago 6
Terrific video, Blaise! My son Nolan has PWS too and knows the struggle of being hungry every minute of every day. Thanks to you and your family for helping to raise awareness. Love the moves, too, you are one little cutie :-)
plantgirl14 2 years ago 5