About this project
WHO?
The five million (plus) Americans who have been diagnosed with gastroparesis..
WHAT?
One book to educate, inspire, and empower those people to become their own advocates and lead healthier, happier lives.
WHY?
Gastroparesis (GP) is a poorly understood digestive condition in which the stomach does not empty food properly. There are very few treatments available and, as of right now, no cure. Sadly, patients are typically provided very little information or guidance upon diagnosis.
I was diagnosed with gastroparesis 7 years ago at the age of 23. In 2009, frustrated by the lack of information available to patients, I started a blog called Living With Gastroparesis. Since then my humble little blog has attracted visitors from over 60(!) countries and I've received hundreds of emails saying things like:.
"I've been looking for this kind of information for years. Thank you!"
"I learned more about my condition on your Facebook page than I did from my doctor."
"Finding your blog has truly kept me sane!" .
Clearly the need for an honest, comprehensive resource about living with gastroparesis is huge, yet there is not a single book available for GP patients. So...I'm going to write one..
HOW?
With your help.
The money being raised here on Kickstarter goes toward the costs of publishing and marketing this book. Basically, you're helping me get this book into the hands of the people who need it and do it as soon as possible. The more funding this project receives, the wider the reach will be.
**PLEASE NOTE** Kickstarter projects are "all or nothing." You will not be charged for your pledge unless the fundraising goal is met.
FAQ
Have a question? If the info above doesn't help, you can ask the project creator directly.
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Funding Successful
This project successfully raised its funding goal on January 19, 2011.
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The gratitude of all of the people worldwide who are waiting for this kind of resource!
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Your name in a special acknowledgement section of the book.
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Your name in the acknowledgement section, plus a DIGITAL copy of the book.
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FRIENDS & FAMILY: Have a loved one with gastroparesis? Your name, their name, and a short personal message will be listed in a special section of the book. They'll also receive a personalized card by mail, letting them know that you supported this project in their honor.
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Your name in the acknowledgement section, plus a softcover copy of the book -- OR -- a "Gastroparesis-Friendly" T-shirt.
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Your name in the acknowledgement section, plus a softcover copy of the book AND a "Gastroparesis-Friendly" T-shirt.
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GASTROPARESIS PATIENT'S PACK: One 50-minute Health Counseling session by phone, plus a digital copy of Eating For Gastroparesis:Guidelines, Tips & Recipes, and a softcover copy of this book when it's published. Your name will also appear in the Dedication section of the book. {Limited number available!}
Project By
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Hi, there. I'm Crystal. I was diagnosed with idiopathic gastroparesis, a poorly understood digestive condition, at the age of 23. The day a doctor looked me in the eye and said "come back when you need a feeding tube," was the day I realized I had no choice but to become my own advocate.
I immediately started to educate myself, not just about gastroparesis but about all aspects of health and wellness. This eventually led to a career as a Certified Health Counselor, educating and empowering other gastroparesis patients to become their own advocates.
