Blaise talks to Oprah About Prader Willi Syndrome

[talkin2ya]

thnx for sharing.

[sherr81]

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.

[renaycompere]

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.

[creamsodaistasty]

@renaycompere unfortuantly, at what cost.

[choforito4000]

This is a GENETIC condition, sadly there's no cure... you can't change the genetic information.

[ArtemisMS]

@choforito4000 stem cell research can perhaps one day help

[choforito4000]

@ArtemisMS I don't think anything can help this guys, maybe in the intrauterine life?

[katmobile59]

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!

[Buggie4Taz]

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

[kitihoku]

Great Job Blaise! My son who is now 4 years old also has Prader Willi. It is always a struggle to keep him off food. We love him so much that it breaks our heart when we see him trying to sneak out food from our fridge. Be safe and always remember that God always look after us.

[56785439]

@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.

[Zwi1122]

Great video!!! Your son is absolutely adorable! My friend at work has Prader-Willi. I think this idea is WONDERFUL; and I'll keep watching and supporting- I hope we can catch Oprah's attention. God bless.

[Zwi1122]

Thank-you for this video! He's adorable. A girl I work with has Prader-Willi. I love her dearly. Keep up the good work- I'll keep watching, and hoping that Oprah gets the message!!!

[BigGriff1000]

cute video. My son Graisen has PWS also, he will be 3 in june..funny enough they dance exactly the same way..LOL..hope this video works!!

[plantgirl14]

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 :-)

[doughtyone]

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.

[ronsmithx1]

Prader-Willi syndrome (PWS) is a genetic disorder that causes (among other things) unregulated appetite, so that little guys like BLAISE (in this compelling video) are hungry all-day, every day -- no matter HOW MUCH they eat.

[hands4health2]

We love you Blaise. We are praying for a cure and praying that Oprah features your cause on her show.