After Megan was diagnosed with idiopathic gastroparesis in 2016, her physical and mental health began to spiral. She was very sick and very scared as she constantly scoured the internet for answers as to why this had happened to her and how she could fix it.

Five years later, Megan still has gastroparesis but her experience of it is totally different. She's now eating things she never thought she'd eat again, but far more importantly, she's free of the fear that used to consume her. In our chat, Megan talks about how she got to this place and shares her advice for those who are currently struggling.
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If this discussion resonates with you, I highly encourage you to check out The Little School of Big Change. It's a 6-week live, interactive course that dives deep into the "inside out" way that our experience really works. I recently wrote about why this is the resource that I wish I'd had when I was diagnosed 16 years ago: https://bit.ly/3NcsGms
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Find my books on Amazon!
Living (Well!) with Gastroparesis: http://bit.ly/gastroparesisbook
Eating for Gastroparesis: http://bit.ly/eatingforgp

Hi, I'm Crystal. I was diagnosed with idiopathic gastroparesis in 2004 at the age of 23. My experience with gastroparesis has run the gamut, from being malnourished, anxious, and all but hopeless to being a healthy, happy wife, mom, and dual-certified coach, truly living WELL!

I really believe that this kind of freedom from the suffering around gastroparesis is possible for -- and available to -- everyone... regardless of the severity of symptoms or how long you've had the condition. I hope you'll come along as we explore what the inside-out approach to living WELL with gastroparesis is and where freedom really comes from.

Join the mailing list at: http://bit.ly/crystalsemail