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

Newbie Just Investigating The Possiblility Of Dm


boysmom

Recommended Posts

boysmom Explorer

I have only recently learned enough about celiac/gluten intolerance/dermatitis herpetiformis to begin to suspect that it may explain a lot of the issues I've dealt with over the last (at least) 10 years. I have only begun the testing process and have an appointment with a gastroenterologist in about a month, but if you don't mind I have a few questions for you while I wait.

I have had a recurring rash over the last 10 years that seems to me like it *could* be DM and I'd like to see if it sounds right to you who have lived through it.

1. Rash first appeared about halfway through my 5th pregnancy (4th pregnancy ended in miscarriage 2 mos before this conception). While it started on my lower abdomen, over the course of 4-6 weeks (and many attempts with creams, ointments, and benadryl) it spread to cover me from the neck down and was beginning to move up the back of my scalp when they finally prescribed a course of prednisone which finally put it at bay. I've read a lot about another drug, but does DM respond to prednisone?

It was excruciatingly itchy and not scratching was NOT an option. Scratching left me sore and bruised feeling, but even that was an improvement.

2. It returned shortly after delivery and seemed to run a course of breaking out for 8 weeks, then slowly improving for 8 weeks, never completely healing, before breaking out again. Each breakout seemed a little milder than the one before and my husband was making some career changes (thus insurance changes), followed by 3 moves in 2 years, which caused me to decide to just wait it out for a while. By the time we'd settled it just quit coming back.

3. It has come back a few times since, but never as severely. Usually it's been just the lower belly area and upper thighs, or only on my elbows or knees. Usually in the heat of summer or the coldest part of winter when I'm spending a lot of time dressed warmly or under heavy blankets.

Another aspect of my rash: Does DM behave somewhat like hives, in that it seems to itch more or spread more when it's warm or constricted? Does it seem to flare when you develop another, unrelated rash? I've had a few times now when I got a light rash similar to poison ivy when I'd been out pulling weeds (NOT poison ivy, because I know what that looks like and don't touch it), but then I proceeded to break out over the next 3 weeks in places that I know had no way to come in contact with the weeds (again, my lower belly, upper thigh area or buttocks). I do wash thoroughly and change clothes when I've been in weeds because I know I am prone to rashes.

I appreciate any insight you can give me, so I can go to my Dr appointment well armed with information and, hopefully, find some answers I can do something about so I can get to feeling better again.


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



Celiac.com Sponsor (A8-M):



boysmom Explorer

And that subject should be that I'm investigating DH... that's what I get for trying to do too many things at once. Sorry :blink:

ravenwoodglass Mentor

If you want to know for sure if it is DH you should go to a dermatologist while the rash is active and ask them to biopsy looking specifically for DH. The biopsy will be done on an area next to the rash not on the rash itself. A diagnosis of DH is a diagnosis of celiac.

You might want to take a printout of this from the NIH with you to show the derm if needed.

Open Original Shared Link

ChemistMama Contributor

ravenwoodglass is correct, do not go gluten free, and go directly to a dermatologist for a biopsy (and do not pass go and collect $200). ;)

DH can be resolved temporarily with steroids, but in my experience (and my dermatologists), the rash just comes back worse later if you're not gluten-free. It itches like a bear and can get worse if you have 'prior skin trauma'. Go here and search "minor trauma to the skin"

Open Original Shared Link

Yes, there is a drug for DH called dapsone. If you're interested, search the forums for 'dapsone' and you'll get a lot of posts. It works great but can also be a nasty drug with unpleasant side effects.

Good luck!

boysmom Explorer

I typed out a nice long reply to this a couple of days ago, then just as I was about to send we had a power surge and my laptop (that doesn't have a battery) shut down and I lost it all :(

I do not currently have a rash. We do not eat a typical American diet, so it's not unusual for us not to eat bread for several weeks, then eat a lot of sandwiches during a busy time, and I'm suspecting that this is why my rash comes and goes more than some? My last outbreak was when we'd made a trip to see the grandmas and had been eating sandwiches all week long. Since the whole idea of watching gluten is brand new to me I don't have any way to measure exactly how the rash and my diet corresponded in the past. This has been going on (off and on) over 10 years. LOL I thought I was doing the healthy thing by grinding my own whole wheat flour and making our home totally white flour free.

I posted a more complete explanation under the Prediagnosis area titled Esophageal Spasms which, I hope, explains why I'm unwilling to subject myself to weeks of eating high-gluten foods to get a diagnosis. As if the simple misery of the rash itself weren't enough to make that an unappealing option ;)

I'm really not expecting anyone here to make a diagnosis, but I would like to pull enough information together to show my doctor and/or the Gi doc so they will take me seriously and help me find the help I need. If the description of my rash does NOT sound to you like DH for some reason, please tell me and explain why so I don't confuse the issue with my doctors by including symptoms that don't apply. While it seems on the surface that nearly every medical issue I've had can be explained by celiac/gluten intolerance, I recognize that in the real world there is often more than one thing going on at a time. I just really appreciate the advice of those who have gone before and can help me navigate these murky waters.

mouse Enthusiast

I had a blistery watery and horrible itchy rash on my fingers since I was a teenager. Once I went gluten free, I have never had the rash again, unless I got accidently glutened. If you see a dermatologist while you have the rash, he can take biopsies and then you would have your diagnosis of Celiac. You can only have DH if you are a Celiac. Just make sure that they do the biopsies on the areas beside the rash and not directly on the blister themselves. I went to dermatologists for years, but they only tested the blisters and not the surrounding areas.

I really think you need a definate answer as it is too easy to go back on gluten, when you begin to doubt your self diagnosis.

Good luck and it is really great not to itch like that anymore.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,962
    • Most Online (within 30 mins)
      7,748

    AlissaW
    Newest Member
    AlissaW
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.