juliesdreamteam
New member
All,
Over a year ago, I became a member of CysticFibrosis.com. I shared the creation of Julie's Dream Team with you all. A team that does nothing but drink beer and eat pizza/wings. To date, our methods of asking those to "Live life...help others live theirs" has generated over $250,000 for CF research. This website was a crucial to providing me with the knowledge I needed as a CF husband. To this community, I am eternally grateful.
One year ago, my Julie was inches away from death. Today, she's doing wonderfully after a double-lung transplant. She's returned to full-time work and she's living life to its fullest, honoring her donor each day.
I wrote her story. I have directed the publisher to send payments to the CF Foundation for research. 100% of the proceeds from the sale of Julie: The Courage to Breathe will go towards finding a cure. I don't need money....I need a cure to realize my Julie's dream and the dream of thousands of others.
My hope is that you all will visit our site: www.juliesdreamteam.com and join the thousands across America (we have a FaceBook group) that have answered the call to live life, helping all of us find the cure that is desperately needed by so many. If you buy the book (and you should), know that we'll never profit from this venture. I know you don't know me from Adam but I know that her story will help inspire others to never give up. It will help others that are married to a cystic (fyi....the editor and I fought over the term "cystic". He said it's not a word. I agreed and told him it's a way of life. We won!) cope and understand that WE CAN BEAT CF!
NEVER GIVE UP! We can cure it. I believe it in my soul.
God Bless...CURECF!!!
Roy E. Ice
www.juliesdreamteam.com
Over a year ago, I became a member of CysticFibrosis.com. I shared the creation of Julie's Dream Team with you all. A team that does nothing but drink beer and eat pizza/wings. To date, our methods of asking those to "Live life...help others live theirs" has generated over $250,000 for CF research. This website was a crucial to providing me with the knowledge I needed as a CF husband. To this community, I am eternally grateful.
One year ago, my Julie was inches away from death. Today, she's doing wonderfully after a double-lung transplant. She's returned to full-time work and she's living life to its fullest, honoring her donor each day.
I wrote her story. I have directed the publisher to send payments to the CF Foundation for research. 100% of the proceeds from the sale of Julie: The Courage to Breathe will go towards finding a cure. I don't need money....I need a cure to realize my Julie's dream and the dream of thousands of others.
My hope is that you all will visit our site: www.juliesdreamteam.com and join the thousands across America (we have a FaceBook group) that have answered the call to live life, helping all of us find the cure that is desperately needed by so many. If you buy the book (and you should), know that we'll never profit from this venture. I know you don't know me from Adam but I know that her story will help inspire others to never give up. It will help others that are married to a cystic (fyi....the editor and I fought over the term "cystic". He said it's not a word. I agreed and told him it's a way of life. We won!) cope and understand that WE CAN BEAT CF!
NEVER GIVE UP! We can cure it. I believe it in my soul.
God Bless...CURECF!!!
Roy E. Ice
www.juliesdreamteam.com