Skip to main content

Eat Like Us

May 24th marks the 5th annual "Eat Like Us For a Day" Challenge, an event sponsored by GAEOS (Georgia Eosinophilic Disorder community) that aims to raise awareness of Eosinophilic Gastrointestinal Diseases (EGIDs).  Even if you've never heard of an EGID before, I highly recommend taking part in this one-day event.

So, what's an EGID?  

EGIDs are chronic conditions of the digestive system that are caused by too many of a certain white blood cell, the eosinophil, congregating in a certain area of the system. These white blood cells respond to some sort of environmental trigger, usually food, and attack it.  Please note that EGIDs are not the same thing as a food allergy, which is caused by a different reaction from the immune system.


The most common place for battle seems to be the esophagus, resulting in eosinophilic esophagitis, but the stomach, small, and large intestine can also be affected.  The symptoms reflect the part of the GI tract affected, and include abdominal pain, reflux, nausea, vomiting, and diarrhea.  Patients also report that they experience other symptoms outside the digestive tract like joint pains, fatigue, and eczema. 

In eosinophilic esophagitis, the esophagus can be damaged pretty severely which can lead to significant narrowing, sometimes even to the point its opening is the size of a straw.  Swallowed food will get stuck and a doctor, usually in the emergency room, will need to go in and remove it.  There are procedures to stretch the opening again, but these are invasive and risky.

Normal Esophagus
Eosinophilic Esophagitis
EGIDs are pretty poorly understood by the medical community, but are getting more attention in recent years.  The number of people newly diagnosed with these conditions is exploding all over the world (Around 1 in 2000 now), and a condition that was once considered one of childhood has shown up repeatedly in adults.  

Treatments for EGIDs are limited and include steroids, either topical (e.g. swallowed Flovent) or systemic (e.g prednisone), and allergy medications (e.g. Singulair). Unfortunately there is an ongoing problem of even the best physicians not having heard much about EGIDs and not being able to identify them when patients come in with symptoms.  It can take years to get an accurate diagnosis, which is something we see in many chronic conditions, but frustrating nonetheless.  

Uh, doc....doc....hello?
Another potential treatment for a person living with an EGID is changing their diet and eliminating the foods that cause those eosinophils to attack.  The top 8 offending foods are:  dairy, eggs, wheat, soy, peanuts, tree nuts, fish, and shellfish.  No problem, right?  There are lots of people who are lactose intolerant or who have Celiac disease.  

Unfortunately, for a lot of people with an EGID, it's not just dairy or wheat or soy, but a combination of several if not all 8 of those foods.  For others, their list expands beyond the top 8 to include anything from lettuce to beef to blueberries to sweet potatoes.  It can take months, or even years, to pinpoint the exact trigger foods through elaborate elimination diets that include removing all food from your diet and living on formula for a while to let things in your system calm down.  


For some, they find out they can only eat a handful of foods without getting sick. 

Imagine the impact that this has on a person's quality of life, no matter what age.  You can experience the EGID diet first hand by taking part in the Eat Like Us day on May 14th, which wraps up National Eosinophil Awareness week.  Check out their Facebook page and join in on the cause.  

Just be sure to read your food labels - dairy, wheat and soy is in just about everything!

For more information about EGIDs please visit two great patient advocacy groups

Best,
Dr. T.

Popular posts from this blog

So You Have IBD During a Pandemic

Hey! What's going on? Been pretty boring over here in Chicago. Ok I don't need to elaborate on what the hell is going on in the world. We are being bombarded with information - some accurate, a lot inaccurate - about this pandemic. It's very easy to become completely overwhelmed by it all. We've been forced, pretty damn quickly, to completely overhaul our way of life for the greater good. To reduce the strain on our healthcare system of the sick and dying. And us humans are generally bad with rapid, monumental change that we really don't have a lot of say in. Our little reptilian brains do what they're supposed to do (prime us for fight or flight or freeze) but our advanced "thinking" parts of our brain have to interject with all sorts of unhelpful thoughts, thereby sending some of us off the rails. Before we start, turn off the news. Seriously. In the days following 9-11 we found people who consumed more 24-hour news channel information were mor

Psychosocial aspects of having an ostomy

This past Saturday, Tiffany and I had the honor of speaking at the United Ostomy Associations of America's Regional Midwest conference. I was assigned the task of speaking to the patients, and Tiffany addressed the partners or caregivers. I wanted to share with you some of the highlights from my talk. I only had an hour for my session, and with about 100 people in the room, it was not nearly enough time. I love bullet points, so here you go: We are all different! Every ostomate is different and not one size fits all for the emotional/mental aspect either. Who had months to talk about an ostomy and weigh pros/cons? Who was this a more sudden decision for? Who had cancer? Who had IBD? Something else? Who had an ileostomy? colostomy? urostomy? Who has a temporary? Permanent? Multiple temporaries? What age where you when you got your ostomy? Under 20, 20s, 30s, 40s, 50s, 60+ Who was single when they got their ostomy? With a serious partner when they had it? Some find a stom

IBD & Medical Trauma

Medical trauma is such an under-recognized issue for the chronnically ill. It's a hard topic to talk about because it can seem like we are pointing fingers at healthcare workers. Maybe that's why there are only, now, 4 studies on the topic in patients with inflammatory bowel disease (IBD). If you are someone who treats people with IBD please know I am not here to demonize or criticize. I am both a patient and a GI psychologist. I know the medical system from both sides. I know how messed up and broken it is. But ignoring this or rationalizing it away as only affecting a few folks is wrong. So let's talk about it. Post-traumatic stress (PTS) is the term we use for medical trauma due to technicalities in the Diagnostic and Statistical Manual for Mental Disorders (DSM-5) for post-traumatic stress disorder (PTSD). PTS can be less severe that full on PTSD, or it can be full on PTSD. Regardless, the symptoms are identical: Feeling hypervigilant/on-edge (increased