It’s been a long couple of weeks. We’ve been busily trying to get the homeschool classroom put together, since Jed has announced that he can only go to school IN a classroom. (Love opinionated kiddos!) Really our classroom is just half of our office cleaned out and dedicated to school … Continue reading →
The end of the year was so busy around here I didn’t write much. Just to keep the story-telling flow going, I figured I’d fill in the gaps for the last few weeks. When I last updated about the boys, Zac had vomited and we didn’t know why. We still … Continue reading →
My son Jed is four and a half years old. He’s bright, funny, charming, sweet, helpful, brave, and all around a very cool kid. He also has Fructose Malabsorption and Salicylate Sensitivity (among other food issues). Two Saturdays ago I made all sorts of yummy treats for him to take to a … Continue reading →
Even though Zac hadn’t returned to 100% baseline, on Saturday, we started re-trialing bananas. He’d gotten increasingly picky, and I was worried about his weight. Hey, it worked for quinoa, right? So far, okay. Saturday he had a good diaper, and no acute FPIES signs. Sunday he was a tad … Continue reading →
This weekend, Zac reached another milestone: sweet potatos are safe!! I. Am. Ecstatic! Sweet potatos are SO yummy and nutritious! After slightly over a week of sweet potatos, Zac’s weekly weigh in was a stupendous 28 pounds!! Plus, this week he’s done his usual “new food developmental leap”. He’s trying … Continue reading →
I’m going to say something that will probably really raise the hackles of Food Allergy Mama’s everywhere: in a straight comparison, I love food allergies and I hate food intolerances. Of course I’d rather not deal with ANY of them, but let’s face it: allergies are easy in comparison. This … Continue reading →
One thing about living with FPIES (and MSPI, Fructose Malabsorption, and IgE allergies), is that often your kids don’t really get to BE kids. Either you can’t go to things that most kids do, like playdates, parties, and activities, or they wind up so restricted by all the food concerns … Continue reading →
Well, it’s official. There are no restaurants at which it is safe for my family to eat. We can never eat out again. (At least, not unless my kids suddenly outgrow at least half of their food allergies.) Last Friday we took the kids to the park. When everyone had … Continue reading →
Last week I was inspired to try something new for Zac. On one of the message boards, someone had mentioned making meringue and piping it into shapes for a safe Easter “cookie” for their FPIES kiddo, and that sounded intriguing to me. We don’t have sugar or vanilla as safe … Continue reading →
Jed, as you may know, has fructose malabsorption. Trying to find foods that are safe for him is quite a challenge – particularly things like sausages, hot dogs, bacon…and condiments. All of those things are typically chock-full of fructose, not to mention fun things like “natural flavors” and “seasonings”. We … Continue reading →
FPIES stands for Food Protein Induced Enterocolitis Syndrome. It is a rare food allergy that affects the gastrointestinal system. Reactions are delayed onset, usually 2-4 hours after a trigger food is eaten, but sometimes even longer than that.
Children with FPIES have symptoms that range from severe (violent vomiting to bile and hypovolemic shock) to mild (bloody diarrhea, sleep disturbances).
There is no test for FPIES. It is diagnosed by clinical observation and ruling out other possibilities.
There also are no tests to determine trigger foods. FPIES parents must simply feed their child a food, then wait to see if they react.
Find out more: Click on "FPIES Links" at the top!
Thanks for stopping by! My name is Carrie. This is where I talk about all things FPIES, Fructose Malabsorption, Food Allergies, Real Food, Recipes, and MCAD. Click on the photo for more on my family and what this blog is about, and thank you for visiting! Be sure to subscribe so you never miss a recipe! (Don't worry, your email is safe with me.)