Gluten Free Cheerios ~ YUM!

I was skeptical. I get very sick on gluten and it can put me down for 3 days. It's horrible and I do anything to avoid it. So when I heard about Gluten Free Cheerios I had mixed feelings. Could it be true??? Could I trust it?

If you go to the Cheerios website, you'll see detailed videos about how they make Cheerios gluten free. They test to keep it under 20 ppm as according to the FDA.
It was interesting but I still wasn't sold. So I turned to the Celiac community for insight.

Gluten Free Watchdog  wasn't too keen on the safety of Gluten Free Cheerios.

Gluten Dude was a little more forthcoming but not exactly positive.

So I reached out to a friend from Sea Shore Celiacs, a support group in my area. One member, a very sensitive Celiac, did a Cheerio Challenge. She ate 3 Cheerios one day, a few more the next, and built up to a whole bowl without getting sick. Then my daughter tried a bowl and was fine.

I've had them for dinner for the past two nights and I'm feeling fine, too.

Like any processed food we try, there is always a chance of the labeling not being exactly honest or the fact that 20 ppm is way too much for Celiacs. How do we know for sure?

eh, I'm eating my Cheerios!

5 Reasons Celiacs Need Other Celiacs

Whether you're newly diagnosed or have known you had Celiac Disease for years, the support of others who understand will make all the difference in your life. It's important to your mental and physical well being.

1. You will keep up on the latest Gluten news. New Gluten Free products will become available or you might learn of something that is no longer considered gluten free.

2. The Celiac community will share tips for keeping your kitchen gluten free and safe. Things like having a new gluten free toaster or electric can opener aren't always apparent to newly diagnosed Celiacs, but are a big cross contamination issues. Tips like this can be learned at in-person and online support groups.

3. Other Celiacs are the best way to find doctors with the knowledge to properly advise you. Not all doctors know enough about Celiac Disease to help you through from diagnosis to wellness. You're going to want the best.

4. Many newly diagnosed Celiacs are completely lost and have no idea what to eat. It's easy to say fruits and vegetables are gluten free, but there is so much more to a healthy diet. You'll want to know how people deal with everything from daily eating to eating out.

5. Aside from the facts of what to eat and what not to eat, a newly diagnosed Celiac will do better if they can connect with someone who's gone through it all. From shopping to parties, the Celiac Community can offer suggestions, recipes and most of all emotional support. These people know what it was like to be blindsided by a diagnosis and then have to cope with family members and coworkers. They can tell you how they handled situations, rude comments, or the confusion that came with their own diagnosis.

Bottom line, don't fear a support group. You just may find new friends to share dinner with, swap Gluten Free recipes with, or just some information that will help you cope. Go ahead, Google a support group in your area.  You'll be glad you did.