New CF Book, AImed at young children with CF

rcq925

New member
JUst wanted to let you all know that another CF mom I know from another board has written and finally gotten published a book about CF aimed at very young children with CF.

Here is a copy of her post on another board:

Yay! It's been a very long and involved process but I am very, very
happy to report that Cadberry's Letters is finally available! Eeeee!
For those that don't know, over a year ago I started writing a
children's book about CF for my daughter. We own almost all of the
books that are out there, but most were aimed at children older than
Cassidy.

Cadberry's Letters uses simple, easy to understand language to
explain CF & treatments in a way that young kids can understand. The
book features beautiful full-page and full-color art showing some of
the medications and equipment that are a part of our children's
lives.

You can see a preview of the book and order it at the following URL:
<a target=_blank class=ftalternatingbarlinklarge href="http://www.lulu.com/content/1648046
">http://www.lulu.com/content/1648046
</a>
Eventually the book will be available on Amazon.com, Barnes &
Noble.com and Borders.com among others. That process will take a
couple weeks however. 100% of all author and artist royalties from
the book will be donated to the CFF.

Also, I'd like to encourage anyone that can to donate a copy to
their local CF center and/or library so that Cadberry can reach as
many families as possible.

If you have any questions about the book, please email me at
jennracek@gmail.com. Feel free to repost any part of this message
whereever you like, I don't mind. I'm going to try to post notices
at some of the major CF boards but I'm certain to miss a lot of
them.

Thanks,

Jenn
Mom to Cassidy, 3yrs w/CF & G-tube


THe book likes fantastic and I cannot wait to get it!!
 

rcq925

New member
JUst wanted to let you all know that another CF mom I know from another board has written and finally gotten published a book about CF aimed at very young children with CF.

Here is a copy of her post on another board:

Yay! It's been a very long and involved process but I am very, very
happy to report that Cadberry's Letters is finally available! Eeeee!
For those that don't know, over a year ago I started writing a
children's book about CF for my daughter. We own almost all of the
books that are out there, but most were aimed at children older than
Cassidy.

Cadberry's Letters uses simple, easy to understand language to
explain CF & treatments in a way that young kids can understand. The
book features beautiful full-page and full-color art showing some of
the medications and equipment that are a part of our children's
lives.

You can see a preview of the book and order it at the following URL:
<a target=_blank class=ftalternatingbarlinklarge href="http://www.lulu.com/content/1648046
">http://www.lulu.com/content/1648046
</a>
Eventually the book will be available on Amazon.com, Barnes &
Noble.com and Borders.com among others. That process will take a
couple weeks however. 100% of all author and artist royalties from
the book will be donated to the CFF.

Also, I'd like to encourage anyone that can to donate a copy to
their local CF center and/or library so that Cadberry can reach as
many families as possible.

If you have any questions about the book, please email me at
jennracek@gmail.com. Feel free to repost any part of this message
whereever you like, I don't mind. I'm going to try to post notices
at some of the major CF boards but I'm certain to miss a lot of
them.

Thanks,

Jenn
Mom to Cassidy, 3yrs w/CF & G-tube


THe book likes fantastic and I cannot wait to get it!!
 

rcq925

New member
JUst wanted to let you all know that another CF mom I know from another board has written and finally gotten published a book about CF aimed at very young children with CF.

Here is a copy of her post on another board:

Yay! It's been a very long and involved process but I am very, very
happy to report that Cadberry's Letters is finally available! Eeeee!
For those that don't know, over a year ago I started writing a
children's book about CF for my daughter. We own almost all of the
books that are out there, but most were aimed at children older than
Cassidy.

Cadberry's Letters uses simple, easy to understand language to
explain CF & treatments in a way that young kids can understand. The
book features beautiful full-page and full-color art showing some of
the medications and equipment that are a part of our children's
lives.

You can see a preview of the book and order it at the following URL:
<a target=_blank class=ftalternatingbarlinklarge href="http://www.lulu.com/content/1648046
">http://www.lulu.com/content/1648046
</a>
Eventually the book will be available on Amazon.com, Barnes &
Noble.com and Borders.com among others. That process will take a
couple weeks however. 100% of all author and artist royalties from
the book will be donated to the CFF.

Also, I'd like to encourage anyone that can to donate a copy to
their local CF center and/or library so that Cadberry can reach as
many families as possible.

If you have any questions about the book, please email me at
jennracek@gmail.com. Feel free to repost any part of this message
whereever you like, I don't mind. I'm going to try to post notices
at some of the major CF boards but I'm certain to miss a lot of
them.

Thanks,

Jenn
Mom to Cassidy, 3yrs w/CF & G-tube


THe book likes fantastic and I cannot wait to get it!!
 

rcq925

New member
JUst wanted to let you all know that another CF mom I know from another board has written and finally gotten published a book about CF aimed at very young children with CF.

Here is a copy of her post on another board:

Yay! It's been a very long and involved process but I am very, very
happy to report that Cadberry's Letters is finally available! Eeeee!
For those that don't know, over a year ago I started writing a
children's book about CF for my daughter. We own almost all of the
books that are out there, but most were aimed at children older than
Cassidy.

Cadberry's Letters uses simple, easy to understand language to
explain CF & treatments in a way that young kids can understand. The
book features beautiful full-page and full-color art showing some of
the medications and equipment that are a part of our children's
lives.

You can see a preview of the book and order it at the following URL:
<a target=_blank class=ftalternatingbarlinklarge href="http://www.lulu.com/content/1648046
">http://www.lulu.com/content/1648046
</a>
Eventually the book will be available on Amazon.com, Barnes &
Noble.com and Borders.com among others. That process will take a
couple weeks however. 100% of all author and artist royalties from
the book will be donated to the CFF.

Also, I'd like to encourage anyone that can to donate a copy to
their local CF center and/or library so that Cadberry can reach as
many families as possible.

If you have any questions about the book, please email me at
jennracek@gmail.com. Feel free to repost any part of this message
whereever you like, I don't mind. I'm going to try to post notices
at some of the major CF boards but I'm certain to miss a lot of
them.

Thanks,

Jenn
Mom to Cassidy, 3yrs w/CF & G-tube


THe book likes fantastic and I cannot wait to get it!!
 

rcq925

New member
JUst wanted to let you all know that another CF mom I know from another board has written and finally gotten published a book about CF aimed at very young children with CF.
<br />
<br />Here is a copy of her post on another board:
<br />
<br />Yay! It's been a very long and involved process but I am very, very
<br />happy to report that Cadberry's Letters is finally available! Eeeee!
<br />For those that don't know, over a year ago I started writing a
<br />children's book about CF for my daughter. We own almost all of the
<br />books that are out there, but most were aimed at children older than
<br />Cassidy.
<br />
<br />Cadberry's Letters uses simple, easy to understand language to
<br />explain CF & treatments in a way that young kids can understand. The
<br />book features beautiful full-page and full-color art showing some of
<br />the medications and equipment that are a part of our children's
<br />lives.
<br />
<br />You can see a preview of the book and order it at the following URL:
<br /><a target=_blank class=ftalternatingbarlinklarge href="http://www.lulu.com/content/1648046
">http://www.lulu.com/content/1648046
</a><br />
<br />Eventually the book will be available on Amazon.com, Barnes &
<br />Noble.com and Borders.com among others. That process will take a
<br />couple weeks however. 100% of all author and artist royalties from
<br />the book will be donated to the CFF.
<br />
<br />Also, I'd like to encourage anyone that can to donate a copy to
<br />their local CF center and/or library so that Cadberry can reach as
<br />many families as possible.
<br />
<br />If you have any questions about the book, please email me at
<br />jennracek@gmail.com. Feel free to repost any part of this message
<br />whereever you like, I don't mind. I'm going to try to post notices
<br />at some of the major CF boards but I'm certain to miss a lot of
<br />them.
<br />
<br />Thanks,
<br />
<br />Jenn
<br />Mom to Cassidy, 3yrs w/CF & G-tube
<br />
<br />
<br />THe book likes fantastic and I cannot wait to get it!!
 
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