Reason #1 why I wrote Changing Fate: to spread the word about cystic fibrosis. I learned that my daughter's friend has CF and I wanted to do something. I didn't have money to donate and I wanted to help in some way. What I didn't know was that I was already helping in an unexpected way...
by being an organ donor.
Organ donations save lives. Hands down. In a sad event that we lose our life, what better way to go than to save another? It's that simple. One signature and a little logo on your drivers license.
There are people out there waiting for organs just so they can breathe easy and live to experience life a little longer. I'd like to tell you about 2 of them (even though I could probably come up with a really really really really long list of others).
The first is Katy Starck Monte. She has cystic fibrosis and is currently waiting for her second double lung transplant. You can learn more about her story here, and support her through #OOMPHforkaty on facebook and twitter.
|My shout out to Katy and the book I'm offering for the giveaway.|
Caleigh Haber also has CF and is fighting to breathe as she waits for her first lung transplant. You can learn more about her story here, and support her through Fight2Breathe on facebook and TeamCaleigh on twitter.
Both of these girls, and countless others, could benefit from spreading the word about becoming an organ donor. Not just people with CF, but many others as well, lose the battle every day.
Changing Fate might not match each individual story, but my hope is that it helps others realize the difference they can make just by learning to be so we can all become something greater together. Hopefully we can change the fate of those precious lives that are being lost.
Please spread the word and feel free to enter the giveaway below. There will be 4 winners!!! Two $10 giftcards to Amazon.com, the paperback copy of my book pictured above, and an e-book copy of the book.
Also, my e-book will be available for 99 cents for the duration of the contest. My purpose isn't to make this about my book, but to spread awareness through my book if it could teach one more person about CF. As always, half of all proceeds will go to the Cystic Fibrosis Foundation for the continuing research in finding a cure.