Hi Everyone!!
The Children's book that I wrote received a high rating from the editor...which is GREAT!!! It really really looks like the book will be published!! I know this is going to have such a positive outcome for children with PFFD and other limb/extremity differences. The publisher is actually talking about 'The next book!!"
With that, I'll need more photos! I have no idea what this "next book" will be...maybe more stories, maybe another young children's book, like this first one. At anyrate, if you are interested in being apart of this "mission," email me privately. I will need a picture of your child doing something he/she loves doing despite the pffd. Something that you never thought he/she would be able to do. Pictures that just have kids showing that they are "normal everyday kids" are great! It's about awareness. Just make sure your child looks happy.
A few things...1. I really want this book to reach all cultures. I can't imagine turning any child away...I haven't yet, so far. But, I do know that I would love to see more of a balance of children with darker skin. I want all children to be able to "see themselves" in this book
2. I'm not profiting from this book...any money made is going to be donated to organizations that help children w/limb & extremity differences and to make more books for our children! My publisher is going to give me a waiver of fees for the pictures. So, please keep that in mind.
My Publisher is Halo Publishing...It's a self publisher, so it does cost me money to do this. Halo Publishing has helped self publishers publish many books including: "Zollie Goes West."
Libbi
Yeah!!
That's terrific news. I can't wait to buy multiple copies.
Beth
Book
Beth, you're so sweet...but remember, with Olivia in the book, you get one free book!! Thanks for all your encouragement through this whole process!!
Libbi
I want to know
My daughter has PFFD and I am interested in your book. What can you tell me????
Being in the book!
Hi!
Thanks for showing interest in being in the book. I am also beginning to work on book #2. Here's all you have to do...
photograph your daughter doing something she loves doing despite having pffd. The picture should show either the limb difference or, if she's wearing a prosthetic, then just make sure that it's obvious that she's wearing on. Then, email the picture to me. It's that simple. I will send a release form that allows your child to be photographed in a published book. I include the child's 1st name only, age at time of picture and the state in which they live.
Thank you soo much! I hope to hear from others, too!!
Libbi
New to the Group
I just found the group and was surprised to find so many of us out there. I am approaching 50 and things have really chaged over the years. I was born with PFFD bilateral with coxa vera of the right hip. I have an identical twin who is "normal". If there is anything I can can do for you, please let me know.
Susie
Buying your Book
I would love to get more info on how to purchase your book, when it is coming out, etc.. Please let me know how.
April