juliesdreamteam
New member
Guys,
For the past 20 years, I've had CF be a part of my life. Reading this forum, while helpful will never lead to a cure.
It's going to take money for research....and you know we're close to CF standing for Cure Found.
For goodness sakes...pick up a copy of my Julie's story: Julie: The Courage to Breathe.
100% of the proceeds are going to the CF Foundation. I could give two shits less about money (excuse the language). I want a cure.
One and a half years ago, we launched juliesdreamteam.com. The idea was so simple it was ridiculous. Ask people to have a beer and help those with CF live. $250,000 has gone directly from companies like Buffalo Wild Wings to the CF Foundation to help all of those that need a cure live longer. Why? Because they see increased market share while helping do something good within their communities. The passion of our CF families is throwing our cause to the forefront. Businesses are equating CF with increased revenues thereby picking our CF Foundation over others that simply ask for a check. And equally as important, these businesses are learning about what CF is....we don't have to tell them that it's a genetic disease...that it comes from your parents....that it's mucus....that there is no cure.
I have poured my heart and soul into helping find a cure. I did it because of my wife's dream of a cure for your children. She has CF and she lived to tell about it.
You all really need to pick up a copy. I promise you that her story will resonate with you but more importantly, you'll learn how to beat it by NEVER GIVING UP!
Julie's story is available in 31 countries...in their language. I'm serious about finding a cure and I'm willing to give every single dime of the profits away. "Alex. The Life of a Child" raised millions for a cure. Millions that allowed a lot of you to be able to read this post. Julie: The Courage to Breathe will allow us to end it.
$6.36 of every paperback goes to the CF Foundation.
$14.53 of every hardback goes to the CF Foundation.
$5.40 of every Kindle and ePub (iBook) reader goes to the CF Foundation.
Julie's amazing story of courage is available at:
www.Lulu.com/spotlight/curecf
www.barnesandnoble.com
www.amazon.com
I'm serious about finding the cure. I hope you all are as well.
God Bless...CURECF!!!
Roy E. Ice
www.juliesdreamteam.com
For the past 20 years, I've had CF be a part of my life. Reading this forum, while helpful will never lead to a cure.
It's going to take money for research....and you know we're close to CF standing for Cure Found.
For goodness sakes...pick up a copy of my Julie's story: Julie: The Courage to Breathe.
100% of the proceeds are going to the CF Foundation. I could give two shits less about money (excuse the language). I want a cure.
One and a half years ago, we launched juliesdreamteam.com. The idea was so simple it was ridiculous. Ask people to have a beer and help those with CF live. $250,000 has gone directly from companies like Buffalo Wild Wings to the CF Foundation to help all of those that need a cure live longer. Why? Because they see increased market share while helping do something good within their communities. The passion of our CF families is throwing our cause to the forefront. Businesses are equating CF with increased revenues thereby picking our CF Foundation over others that simply ask for a check. And equally as important, these businesses are learning about what CF is....we don't have to tell them that it's a genetic disease...that it comes from your parents....that it's mucus....that there is no cure.
I have poured my heart and soul into helping find a cure. I did it because of my wife's dream of a cure for your children. She has CF and she lived to tell about it.
You all really need to pick up a copy. I promise you that her story will resonate with you but more importantly, you'll learn how to beat it by NEVER GIVING UP!
Julie's story is available in 31 countries...in their language. I'm serious about finding a cure and I'm willing to give every single dime of the profits away. "Alex. The Life of a Child" raised millions for a cure. Millions that allowed a lot of you to be able to read this post. Julie: The Courage to Breathe will allow us to end it.
$6.36 of every paperback goes to the CF Foundation.
$14.53 of every hardback goes to the CF Foundation.
$5.40 of every Kindle and ePub (iBook) reader goes to the CF Foundation.
Julie's amazing story of courage is available at:
www.Lulu.com/spotlight/curecf
www.barnesandnoble.com
www.amazon.com
I'm serious about finding the cure. I hope you all are as well.
God Bless...CURECF!!!
Roy E. Ice
www.juliesdreamteam.com