Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Other Food Sensitivities


Jaxonthehuman

Recommended Posts

Jaxonthehuman Rookie

To those of you who flare up with things other than gluten..... how did you come to learn what they were? was it through elimination? or did you have some sort of test performed by an allergist? The reason I ask is because I have an appointment with an allergist on Friday, and if any of you had luck with a method that is commonly used in that field, I'd like to ask for the same test. I feel that my case is severe (in that I wake up with bloody sheets daily and I have at least a few hundred individual sores). I am in the process of transforming my home into a completely gluten-free home. I bought all new cookware and now have my dog on a gluten-free diet. My girlfriend is also gluten-free.

I am not responding to a gluten-free diet.

I tried Dapsone, Prednisone, and am now on Sulfapyridine.

I have not had any luck with any of these medications.

I cannot sleep for more than a few hours at a time because I wake up scratching. I take benedryll to sleep but it only helps a little. I have been living like this for a few years (since I first developed the rash) and it's exhausting, as I'm sure you all know.

I have checked all my meds, shampoo's, ect.

I also did an 18 day juice fast last summer which did not help.

Any suggestions? Anything I could ask my allergist for?

I am also established with a Dermatologist and see him regularly, but Friday will be my 1st time with an allergist.

I am aware it can take up to a few years on a gluten-free diet but it seems like I would have seen even just a little improvement with the meds and a gluten-free diet by now.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



mushroom Proficient

Are you making sure to limit your iodine intake, which aggravates DH? Iodine is found in, among other things, eggs, shellfish, iodized salt. A quick google will identify other sources. You need to minimize your iodine intake until the current flare stops. I have not had DH, but I understand it can be miserable. I have psoriasis, which isn't a lot better :) But psoriasis isn't affected by iodine :P

itchy Rookie

Jaxon, this probably sounds patronising, because you've been dealing with this for so long. It's not intended to be.

But given that your disease sounds like DH, it should be responding to a gluten free diet by now. I don't know if other conditions cause the bleeding and itching, but DH is certainly a very likely cause.

Given that, are you sure you've got all the gluten out? Did you try my earlier suggestion of finding a 'mentor' to have a look at what you are eating to try to spot if there is some risky food that you are still eating. All of us have missed things that came to cause us grief at some point.

Sorry, that's all I can come up with.

squirmingitch Veteran

Jason, are you SURE the dog is on a gluten free diet? I was feeding my dog Orijen Regional Red grain free (therefore gluten free) & she began having problems with it. Then I saw a YouTube video of the Gluten Free Fox doing an elisha (sp?) test for gluten on it & it turned up high positive. I finally turned to ZiwiPeak air dried raw. They don't make ANY food with grains in it so it shan't be cc. Also got her the ZiwiPeak jerky for treats. Costs like rip but can't cook for her at the moment with this tiny place we are renting. Also --- got some gluten free dog shampoo --- It's EO for Dogs. Besides the dog getting glutened; We can get glutened when we bathe the dog with shampoo containing gluten.

dilettantesteph Collaborator

I don't know what your gluten free diet is like. You may be one who reacts to the allowable amounts. Have you tried a diet of produce and unprocessed meat?

If it is DH, the blisters come from gluten antibodies and iodine. It won't flare up from other food intolerances.

Jaxonthehuman Rookie

Jaxon, this probably sounds patronising, because you've been dealing with this for so long. It's not intended to be.

But given that your disease sounds like DH, it should be responding to a gluten free diet by now. I don't know if other conditions cause the bleeding and itching, but DH is certainly a very likely cause.

Given that, are you sure you've got all the gluten out? Did you try my earlier suggestion of finding a 'mentor' to have a look at what you are eating to try to spot if there is some risky food that you are still eating. All of us have missed things that came to cause us grief at some point.

Sorry, that's all I can come up with.

Yes. I went to a support group and will continue to go (it's only once a month). I also met with a nutritionalist. I don't even eat packaged foods if they were made in the same facility as gluten. I feel like Im doing everything except I found the low iodine diet to be a challenge and didn't do it for much longer than a week. Maybe I should give it another shot.

Jaxonthehuman Rookie

Jason, are you SURE the dog is on a gluten free diet? I was feeding my dog Orijen Regional Red grain free (therefore gluten free) & she began having problems with it. Then I saw a YouTube video of the Gluten Free Fox doing an elisha (sp?) test for gluten on it & it turned up high positive. I finally turned to ZiwiPeak air dried raw. They don't make ANY food with grains in it so it shan't be cc. Also got her the ZiwiPeak jerky for treats. Costs like rip but can't cook for her at the moment with this tiny place we are renting. Also --- got some gluten free dog shampoo --- It's EO for Dogs. Besides the dog getting glutened; We can get glutened when we bathe the dog with shampoo containing gluten.

I give the dog Wellness Core dog food which was reccommended by someone from this forum and her treats are human food. He same thing I eat. Turkey breast and such.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Jaxonthehuman Rookie

I don't know what your gluten free diet is like. You may be one who reacts to the allowable amounts. Have you tried a diet of produce and unprocessed meat?

If it is DH, the blisters come from gluten antibodies and iodine. It won't flare up from other food intolerances.

I though DH was "most often" related to gluten antibodies but sometimes triggered by something else? I'm looking for that. Something else.

Hopeful1950 Explorer

After getting the run around from 3 dermatologists, I consulted an allergist because I was sure something I was eating was causing my rash. The allergist helped me figure out it was DH. He did skin testing where they test for common allergens. They look at everything: pollens,molds,animal dander,foods. They asked me to bring in small amounts of things that I suspected were causing the problem and they included them in the testing. They also did some bloodwork and a 24 hour histamine test(urine). As it turns out, I didn't have an allergic reaction to anything and that, combined with other symptoms I was having, led us to the diagnosis of DH.

I have been strictly gluten free for about 16 months and I am still having flares. When I first started the diet, I was unaware of the iodine connection. I was relying on eggs, especially when travelling, and my rash was getting worse and worse. Then I discovered the iodine connection. When I eliminated it, things got better, but still have not resolved. In your case I'd definitely go ahead and do the allergy testing, but also eliminate iodine. Eggs, asparagus, seafood, vitamins, some medications (both oral and topical).

If you have DH/celiac the antibodies that were formed when you were consuming gluten can remain in your skin for up to 10 years. It seems most people are able to heal their rash in about 24 months, but there are some unlucky people who suffer longer.

FYI, in addition to the skin, blood and urine allergy testing they also might do patch testing where they test for contact allergies. A note on contact allergies: One thing I have discovered is that I can't use preparations with pramoxine in them. Things like Neosporin+Pain or Sarna lotion. They really work to kill the itching/pain, but they make my lesions and the skin around them blister more. Take a careful look at what you are using to get relief from your discomfort. Change it up. Another thing that made things worse was the Aveeno bath soak that one dermatologist recommended. No, No, No. Don't do it!

pricklypear1971 Community Regular

I though DH was "most often" related to gluten antibodies but sometimes triggered by something else? I'm looking for that. Something else.

Salicylates. Bromines. Those are the two things I've heard are related to DH and can be triggers.

Google them and see if one rings a bell. Sals are seemingly in everything, and seem to be cumulative.

I know the low iodine diet is restrictive, but if its part of the problem you've GOT to reduce it. It made me flare by itself. No gluten cc required. You won't always have to be li, just until it calms down.

Bubba's Mom Enthusiast

After going gluten-free I found I was reacting to soy, and maybe dairy?

I went to my allergist, who was treating me for seasonal allergies, and asked about food allergy testing. He did a panel for 90+ allergens via skin prick tests. I didn't react to anything. Then, he did the blood ELISA test for the 8 most common allergens. I got negative results on those too.

I asked him how that could be, since I clearly react to gluten and soy? He said there are NO reliable tests for intolerances, other than removing them from your diet and see how you do. Then, at a later date try them again and see if you get a reaction. If you do, you've discovered your intolerance.

I learned what I was reacting to by keeping a log of everything I ate and noting any symptoms I had. Many reactions are delayed, sometimes by an hour or as much as a day or two! Having a way to go back and figure out what's getting you is very helpful.

Good luck to you. You've been having a rough time for a long while. I hope you can get some relief.

Jaxonthehuman Rookie

Thanks for your input everyone. I think the best thing for me to do is eat a paleo diet of unprocessed meats and fruits and veggies. I know spinach and potatoe skins and asparagus are high in iodine so I will avoid those. I will also avoid dairy of course. And soy. And I will only eat at home so that I can know for sure that my seasonings are iodine free. Perhaps I will post a few pictures later today so you can see the rash I'm talking about. I sure hope this helps. Thanks again.

ciamarie Rookie

It looks like I found this thread a bit late, and the paleo diet may be very helpful. I've discovered that MSG causes my DH to flare. I knew it wasn't from gluten (different symptoms) and I didn't think it was iodine since I'd been pretty low-iodine for weeks, but eating whole eggs didn't cause a reaction. Here's a thread where someone mentioned a flare-up after eating something with MSG, and I mentioned my theory:

pricklypear1971 Community Regular

It looks like I found this thread a bit late, and the paleo diet may be very helpful. I've discovered that MSG causes my DH to flare. I knew it wasn't from gluten (different symptoms) and I didn't think it was iodine since I'd been pretty low-iodine for weeks, but eating whole eggs didn't cause a reaction. Here's a thread where someone mentioned a flare-up after eating something with MSG, and I mentioned my theory:

Yes, I second (or third) the MSG. I ate some stuff with an MSG-type additive in it (there's a group of them) and it was ugly.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,547
    • Most Online (within 30 mins)
      7,748

    gizmo1jazz2
    Newest Member
    gizmo1jazz2
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.