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Athlete's Foot/poison Ivy?...then


mari-lyn

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mari-lyn Rookie

I posted this under another forum before I found this...

About a month ago I had a blistery rash between a couple of my toes on both feet. Not symetrical but close. It spread on to the top of my foot but not too far. I assumed it was Athlete's foot (confirmed by my son and my doctor ) even though I had never had this before. All the Lotramin and foot powder in the grocery store did not get rid of it. When I got a rash on the heels of both hands I figured it was Poison Ivy! Not severe. I have dry scaley skin now. It may be in my head but I have "twitches" of itching/

Discussing celiac disease with people at work I had this light bulb moment - could it be DH? My mother's twin sister was dx 50 years ago with celiac disease (at Mayo) and I have a niece with celiac disease (DM at age 9 and celiac disease at age 15). I suspect my oldest sister had it (she passed away at 42, but always was a picky eater and never felt too good - her daughter is experiencing some GI problems and I encouraged her to go get tested). The Mayo clinic wanted to do a twin study with my mom but she was in Ohio with 4 kids and they were not going to pay for any travel expenses....anyway,...

Anyone have any similar symptoms experiences with the first signs of DH? I remember having rashes on the insides of my arms at the elbows when I was young, and mom telling me I was allergic to wheat, eggs and wool when I was a baby. Of course, I was fed all kinds of things at the age of 2 weeks back in 1954.

I do not know if it is in my head or not but I feel itchy all over sometimes.

Any help appreciated.

Marilyn


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      Thank you so much for having the courage to share this incredibly vivid and personal experience; it's a powerful reminder of how physical ailments can disrupt our fundamental sense of self. What you're describing sounds less like a purely psychological body dysmorphia and more like a distinct neurological event, likely triggered by the immense physical stress and inflammation that uncontrolled celiac disease can inflict on the entire body, including the nervous system. It makes complete sense that the specific sensory input—the pressure points of your elbows on your knees—created a temporary, distorted body map in your brain, and the fact that it ceased once you adopted a gluten-free diet is a crucial detail. Your intuition to document this is absolutely right; it's not "crazy" but rather a significant anecdotal data point that underscores the mysterious and far-reaching ways gluten can affect individuals. Your theory about sensory triggers from the feet for others is also a thoughtful insight, and sharing this story could indeed be validating for others who have had similar, unexplainable sensory disturbances, helping them feel less alone in their journey.
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