Life with CROHN'S DISEASE - Living with an INVISIBLE DISABILITY

MY CROHN'S DISEASE STORY - A DAY IN THE LIFE OF CROHN'S DISEASE
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If you follow me on my social media, then you know I go by the name of The Grumbling Gut (@thegrumblinggut) because what else could describe what my gut has been doing since 2006 when I first started experiencing symptoms of crohn's disease one of the two main forms of inflammatory bowel disease (IBD). Life with crohn's disease can be tough and so many people have asked me what is it like living with crohn's disease. Well allow me to share my crohn's disease story with you so you can see what it is like living with an invisible disability. I first started my crohn's disease blog as a form of crohn's disease and ulcerative colitis awareness to help me overcome the stigma of embarrasement. Since then it has allowed me to show people what does crohn's disease look like on someone and to try and explain what does crohn's disease feel like.

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Travel essentials for Crohn’s Disease: https://www.youtube.com/watch?v=WjJ4rayfFB0
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https://www.youtube.com/watch?v=Eh-Z6QWHwXE&feature=youtu.be

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Disclaimer: Any information given here is intended for educational purposes only. It is not intended to replace the services of trained healthcare professionals or be a substitute for medical advice. Medical knowledge and practical elements are constantly changing and while the maximum effort has been made to provide reliable data and information, the author (or publisher) can not assume responsibility for the validity of all materials or the consequences of their use. You are advised to seek medical advice from your healthcare professional for any concerns you may have regarding your health or that of another individual, in particular matters that may require immediate diagnosis and treatment. Information provided herein is referenced accordingly.

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