Jay Gironimi (rhymes with astronomy) is a man who can't eat and can't breathe. He wrote a book about how that's working out for him. Can't Eat, Can't Breathe and Other Ways Cystic Fibrosis Has F#$%*d Me is not an inspirational story of triumph over adversity. But if you like stories about poop and mucus, it just might be the audiobook for you.
©2013 Jason Gironimi (P)2013 Jason Gironimi
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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