Moms & Children Share Their Journey’s of Diet & Disease
The goal of this blog is to provide insight, tips, recipes and to answer as many questions as we can about Inflammatory Bowl Disease (IBD), the SCD diet and the role nutrition and food play in healing.
In addition, Caleb and other children will be blogging about their experiences not only living with their disease, but what it’s like as a kid to be on a special diet. So, Subscribe to get the latest of Caleb’s Blog.
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Find Out Why Johanna Had to Bring All Her Own Food to Camp Oasis
Johanna Lane writes for Caleb's Cooking Company, but is presently at Camp Oasis in West Virginia, hopefully having a blast! Her mom Catarina Bannier, who is also a contributing blogger, decided to update us in [...]
Amber’s Crohn’s Story, Part 2: There is a Smell to Death
Earlier this week, we shared Part 1 of Amber's Crohn's story, entitled Living With Crohn's: I Thought I was Watching My Son Die. Here is the dramatic ending to Amber's story. November 30, 2016 [...]
Living With Crohn’s: I Thought I Was Watching My Son Die
Amber Hixson is mom to 9-year-old Braxton, who is living with Crohn's and is on the SCD Diet. Amber's story is a heart breaking one. I sobbed when I read it, but unfortunately it [...]
I Turned 13 Last Week, 4 Years Since I Was Diagnosed With Crohn’s Disease
I turned 13 last week, 4 years since I was diagnosed with Crohn's Disease. I decided to look at my journal from this year, and my most recent entry was this poem, which I thought [...]