We all come with a little extra baggage.
Mine happens to be a bit more literal. This is my life documented as I struggle with Ulcerative Colitis, an ileostomy and a JPouch. I’m going to be as genuine and authentic as possible, without holding back any details. I believe in the power of sharing our stories in an effort to build compassion, understanding and empathy.
Hey cool blog, love what your doing! just started my own blog after being diagnosed with UC this year.
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Yay for you! Im sure your openness will be helpful to many of us. I am a newbie and mine is suppose to be reversible, but who knows??
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Nice BLOG! Being almost one year post op, I bet you finally have all your energy back. I’m very happy for you! I struggled with UC and had an ileostomy for 11 years so I know the challenges you are facing and will continue to work through.
I’m an advocate for an alternative surgery that has had a very positive impact on my life (bag free for 2 years now)! I highly encourage you to email me for more information, if interested.
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Thank you for taking this step to help raise awareness Stacey, I know it can’t be easy but you are definitely going to help others!
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I am so impressed by your candour. God bless you, always.
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So proud of you! Love you. .. tons of prayers and support are headed your way!
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