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The Crazy Creole Mommy Chronicles
The Crazy Creole Mommy Chronicles

Tackling Mommyhood One Tantrum & Flareup at a Time

Tag: education

Some Heroes Wear Colostomy Bags

Posted on July 3, 2014July 3, 2014 By Brooke Abbott Abron

Whether you are apart of the Inflammatory Bowel Disease community or not, by now you’ve probably heard of Bethany Townsend, the former model who bared her two colostomy bags at the encouragement of her husband while on vacation. Her picture came across my timeline from The Colitis & Crohn’s UK…

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Tricky Business of Feeding The Baby

Posted on June 30, 2014 By Brooke Abbott Abron

The first time someone brought up feeding Hippo solids, it felt like a needle scratching the album. Cereal! Puree! Breastmilk! Allergies! Formula! Ounces! Spoonfuls! AAAAAHHHH!!! Feeding your child from your breast or going along the instructions they give you when you leave the hospital about creating formula bottles, is pretty…

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Life As I Know It

Posted on June 28, 2014 By Brooke Abbott Abron

It’s been weeks since you’ve heard from me. Mostly because it’s been weeks that I have functioned without some sort of challenge. Let’s see the last you heard from me I had received my first Remicade infusion treatment. That is when it all got rather…nutty, as Hippo would say. Within…

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Infusion Madness

Posted on June 3, 2014June 3, 2014 By Brooke Abbott Abron

June 3rd, 2014, 3:30am: I look at the clock on my computer, that’s what it reads. It’s late…or rather it’s early. But I smile because I can finally feel my eye lids starting to droop. Once again it’s been a night of chronic pain and no sleep. It’s also the…

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Living To Fight, Fighting To Live

Posted on May 14, 2014June 3, 2014 By Brooke Abbott Abron

I was just about to go bed. I had put on my pajamas and was drinking my last sips of water when I checked Facebook for the last time. It’s World IBD Day, so I was just looking for some more updates from people in the community and some of my…

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5 Things You Shouldn’t Say To An IBD Patient

Posted on April 11, 2014 By Brooke Abbott Abron

The experience of living with a chronic illness doesn’t just effect the patient, but also their parents, spouses, friends, family, caregivers and children. Everyone is trying to figure it all out and wanna help. And for the most part, the patient is grateful for the support. But with the everyday…

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