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This book was basically me telling me about my life just in a different voice, with a different name, and with different experiences. Also being held hostage by my lungs everyday of my life, I found that there were a ton of feelings that Jay and I had in common. What an amazing representation of just how many times I want to say "fuck it, or fuck them" when dealing with certain aspects of my CF. I've recommended this book to just about everyone I know over social media and face to face. I've done so because like Jay had mentioned, I am also horrible at expressing my feelings towards this Swamp Thing of a disease in a healthy way with friends and family. This book could do a much better job than me just bitching about my day with Shit-stic Fibrosis. Thank you Jay.
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