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 start a business for himself and other kids, providing food that looks (and possibly tastes, though I haven’t been able to try any of it yet) like the normal food every other kid his age is eating. Kudos to him for thinking of something so creative, I only came up with a blog :).
Caleb is now working together with his mom, Cindy, to make his dream a reality. In addition to his website, Caleb also has a YouTube channel where he’s been posting recipe tutorials, different explanations and pretty much vlogs about his experiences on the diet, and even one pretty cool video about my story, which you can see on none other my “My Story” page. And even if none of that convinced you to check out their new site, they post both Caleb’s and my blogs on there, so there’s already something familiar on the page! Best of both worlds, right? 🙂 I always love hearing other people’s stories on Crohn’s and the SCD, and so does Caleb, so he added a section of his website called Caleb’s Club where kids on the diet can talk to each other all the time. I’m excited to read what Caleb has to say and become a part of his club as well. Congrats to both of you!