This is a guest post by a special supporter because Johanna is in West Virginia at Camp Oasis, a summer camp for kids with Crohn’s and colitis. At intake, Johanna got a huge high-five from the medical team when they realized her medication list was… empty. … More “Really? No Meds? – High Five, Girl!”
Woah. It feels like just yesterday, I was sobbing because I thought I would never be a normal kid again. I know everyone says that “it feels like just yesterday” thing about every big achievement and everything, but it really does. And maybe it’s because I really haven’t changed that drastically. I mean I’ve grown … More Six Months!
Yesterday, my best Crohnie friend (who happens to be my dance teacher), Marnina Cowan, gave me two awesome new shirts; one for this summer, one that raises IBD awareness (though I can obviously wear them all the time!). They’re also really cute, and big enough for me to grow into them, so that’s a plus… … More New IBD Shirts!
Congratulations to Cindy and Caleb for finally making their website public. Go ahead, check it out. I’ll tell you why: Caleb, a 14 year old boy with Crohn’s disease, is on the SCD as well. He has been on the diet for a year, and a couple of months ago he realized that he wanted to … More Caleb’s Cooking Company Is Now Live!
This week, I decided to interview a new friend of mine, Addy. Addy is eleven years old, has Crohn’s disease, and is on the SCD, too. (And even though she was very seriously ill before, she’s now been in remission for more than a year–all without meds!) Even though she lives on the other side … More An Interview With Addy