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

Relapses And Complete Erradication Of Symptoms


brizzo

Recommended Posts

brizzo Contributor

just a question for all of those with dh. Question # 1...upon starting the gluten-free diet, how many "outbreaks" or relapses did you all have while on a 100% gluten-free diet. Question #2 ... how long where you gluten-free untill your skin symptoms where completely gone w/o relapse? Or will we always have occasional "outbreaks" here and there?

  • 4 weeks later...

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



Celiac.com Sponsor (A8-M):



SarahTorg Apprentice
just a question for all of those with dh. Question # 1...upon starting the gluten-free diet, how many "outbreaks" or relapses did you all have while on a 100% gluten-free diet. Question #2 ... how long where you gluten-free untill your skin symptoms where completely gone w/o relapse? Or will we always have occasional "outbreaks" here and there?

I'll be watching for responses, because I'd like to know too!

teebs in WV Apprentice

Well, I have to start off with the obligatory "everyone is different". I was diagnosed with DH last October and immediately changed my diet to gluten-free and also began taking dapsone. Although, as you know (and if you don't you will learn) it took a few months before I really understood how difficult the diet is at the beginning. There were many things that I ate that I thought was ok, but later found out they were not. I am now very carefuly and know what to look out for. I am now a nut about it and make sure there is no way any of my food is contaminated by gluten in our home (my own butter container, peanut butter container, toaster, jelly, lunch meath, cheese, etc.)

Anyway, here's my story pertaining to what you really asked. As I said above, I started taking Dapsone immediately after being diagnosed. Without it, my outbreaks would have continued (even following the gluten free diet). As a matter of fact, I still had intense itching for about 11 months (but did not have the blisters). It has just been within the past month that I haven't itched like crazy. My dermatologist increased my Dapsone dose about a month ago and that seemed to help tremendously.

I am afraid to stop taking it, or to even decrease it. I assume that if I eat anything with gluten I will have a reaction, but I have no intention of testing it to see what happens. I would NEVER want to go through that again!

Hope my ramble helped you in some way - I am sure others who have lived with the disease longer can provide some different points of view.

Take care,

Tracy

angmoore Newbie

Who should I get my daughter to see first - a dermatologist or an allergist? She can scratch herself and get welts - no rhyme or reason it seems to me for the breaking out in hives. We're 90 miles from her celiac disease and Diabetic doctors, but we have a diabetic appointment in a couple of weeks. It would be great if I could get something scheduled on the same day. I just have no idea right now who to see first. Thanks!

teebs in WV Apprentice

My dermatologist is the one that diagnosed me - he took one look at me and said he was very sure that was my problem (this was the first time I saw the guy - I was very lucky, I know). DH is not an allergy - so I would assume you should take her to a derm. They can do a biopsy if they think that is what it is. However, hives is not the same as a DH outbreak. DH is blisters - I mean oosy gross blisters that itch like crazy. After my DH started to get under control I did get hives, which isn't much better, except they don't leave the scars that the DH blisters did.

I hope you find her problem - I hate for anyone to go through it - especially little ones. I don't know what I would have done if my kids would have went through what I have.

Tracy

  • 2 weeks later...
Sophiekins Rookie

With the caveat that everyone is different, here's my story: I was diagnosed with celiac disease and DH in July 2000. By that time, I had lived with atypical presentation of acute DH all over my legs and arms (though not, thank god, on my face) for seven years - if I went out less than fully covered, throat to wrists to toes, people stared and whispered. I promptly cut ALL potential sources of gluten out of my diet - wheat rye oats barley spelt kamut millet buckwheat amaranth arrowroot, as well as corn and soy (1/3 of celiacs will have 'celiac' reaction to corn and/or soy. . .though they do not 'technically' contain gluten, they contain similar proteins that some celiac systems lump in with gluten). I thought I was pretty successful, as the digestive symptoms disappeared quite quickly, though I may have experienced some CC as I was living in a busy bread-loving house at the time. I couldn't take either of the standard drug therapies (liver problems), and so have not taken prednisone or dapsone, and can't speak to their success. A strict gluten-free diet eliminated the itch (I can now identify gluten contamination by the prickling in my skin after a meal) but to say that the skin lesions are slow to disappear is an understatement. From a pharma perspective, I did have limited success with a daily dose of antibiotic (the one they use commonly for staph infections was the most successful, it almost eliminated the fluid coming from the blisters - though they were tested for staph and were negative - and the skin started to heal) combined with a gluten-free vitamin B supplement. . .I believe it was a two week course of 50mg antibiotic and the standard otc oral vitamin B, rest for two weeks and repeat once (though this is not a long-term solution as the antibiotics are, on the whole, bad for your system).

In terms of relapses: The frequency of your relapses will depend on how strictly you adhere to the gluten-free diet - in my experience with DH sufferers, every time you slip, you will have a relapse, and the severity of your relapse may not be related to the severity of your slip. In my case, one tiny slip after a prolonged slip-free period provokes a dramatic relapse, but a series of further slips makes little difference to the intensity of the relapse, only to the duration.

With regards to the complete eradication of symptoms, I have bad news and good news.

The bad news: the DH-causing protein remains active in your bloodstream, causing immune problems for up to thirty days after ingestion. This means that every time you eat a tiny bit of gluten, your non-gluten-free status gets reset for thirty days. Slip once a month, and you may never be truly gluten free. This is why so many DH sufferers find themselves stuck on Dapsone and unable (or too terrified) to go off it.

More bad news: DH sufferers typically react not only to injested gluten, but also to aspirated gluten (breathed in) and contact gluten (proteins in detergents, lotions, etc). So check your shampoos, cosmetics, soaps, deoderants, perfumes, colognes, lip glosses/balms, shaving creams, air fresheners, toothpastes, mouthwash, prescription drugs, otc medicines, laundry soap, fabric softeners, lotions, sunscreens, tanning creams, bug repellants, hand soaps (watch out in particular for ones that are vitamin enhanced - these are BAD), eyedrops, contact lens solutions, nasal sprays, and anything else that you put on any part of your skin or mucal membranes. Next, look for potential sources of aspirated gluten: avoid bakeries that produce non-gluten-free breads, skip the aisle in the grocery store with open shelves of baked goods, stay out of those quaint authentic pizzerias where they toss dough around. . .anywhere you might find flour in the air. Then go through your workspace (since you spend much of your day here, this is a worthwhile thing to do, although it may make you uncomfortable and your coworkers may not understand how serious this is): you need to separate the items you use regularly from people who regularly handle gluten - and this means most of your coworkers and cleaning staff. If a third of people don't wash their hands after using the toilet, how many people wash their hands after eating a sandwich? I recommend getting your own keyboard and mouse (and phone, if you use this for more than a third of your day) and being absolutely anal about not letting ANYONE but you use them - this includes coworkers who just want to show you something for a second, and tech support guys coming to fix your computer. Ask people to talk you through the task instead, and if they ask for an explanation, explain that you have a serious medical condition that is triggered by contact with common substances and that they could make you seriously ill. It's the truth. Also make sure that your managers (and coworkers) are aware that your workspace is off limits to others when you aren't using it - I've found that the simple expedient of locking up my keyboard when I leave the office is enough to keep my workspace empty.

The Really Bad News: your skin takes seven years to completely replace itself, flesh to surface. This means that there could be up to seven years of damage under the worst of your skin lesions. 'Nuff said.

The GOOD News: I have lived largely gluten free for the last six years. I have the occasional significant relapse - usually about once or twice a year, and usually accidental - and minor ones about once a month (when minor relapse is defined as existing lesions oozing and reddening for a few days). Six months ago I took the opportunity to eliminate gluten entirely from my living environment (bye bye bread-eating roommates), and my skin improved so much that it looked better each day when I got up than it had the night before when I went to bed. Hard? Definitely. But on the sixth anniversary of my diagnosis, my partner and I went out to dinner (at a restaurant where the chef is married to a celiac) and I wore a short dress with no sleeves - baring smooth clear skin (bar a handful of scars from the worst of my DH lesions) on my arms and legs.

The End Result: eliminating ingested gluten from your diet SHOULD prevent further damage from happening. The good news is that this isn't so hard once you get the hang of it. Eliminating contact gluten from your life will clear up the existing problems and prevent future ones from occurring. Unfortunately, this requires dedication and constant vigilance. My best guess: eliminate ingested and contact gluten, educate your family, friends and coworkers, hydrate, get plenty of sleep and vitamins (you are rebuilding your body, after all) and you could be all clear in as little as six months or a year. Maybe sooner, if Dapsone works for you, though I would talk carefully to your doctor and your pharmacist - it has NASTY side effects.

Good luck! (And apologies for the length of the post!)

ravenwoodglass Mentor
I promptly cut ALL potential sources of gluten out of my diet - wheat rye oats barley spelt kamut millet buckwheat amaranth arrowroot, as well as corn and soy (1/3 of celiacs will have 'celiac' reaction to corn and/or soy. . .

You have given some excellent info here. I also have DH and know it can take a very long time for an outbreak to heal. Some of mine have taken up to 5 months.

I do want to ask if you can tell me why buckwheat is included in the foods to avoid list. It has been my understanding that buckwheat is actually a grass. I consume it all the time with no gluten reaction. Have I been glutening myself without knowing it?


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



Celiac.com Sponsor (A8-M):



Michi8 Contributor
You have given some excellent info here. I also have DH and know it can take a very long time for an outbreak to heal. Some of mine have taken up to 5 months.

I do want to ask if you can tell me why buckwheat is included in the foods to avoid list. It has been my understanding that buckwheat is actually a grass. I consume it all the time with no gluten reaction. Have I been glutening myself without knowing it?

Buckwheat is not a grain, and is on the safe list. You can keep on eating it! :)

However, it is on the "avoid" list for those who have dermatitis that is related to nickel allergy...in that case, it may need to be eliminated from the diet for awhile and then introduced once symptoms have disappeared.

Michelle

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.