Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Possibly DH?


Assumption

Recommended Posts

Assumption Newbie

Hi all,

 

I just got a call from my (mildly) autistic son's pediatrician, telling me that the follow-up bloods to check his low iron levels show that not only is he still low on iron, he had high levels of all 3 markers for celiac disease. So he'll be referred to get a biopsy.

This kinda got me thinking though. After doing a little googling, I've discovered the existence of DH. Might I have it? If my son has celiac disease then it's entirely possible I have it too, given our shared genes. And I have some skin problems that have plagued me about 20 years...

Since about age 12 (ish), I've suffered from something I simply refer to as "The Itchies." It has come to dominate my life. Some days it persists for hours, but most days it's hanging round the corner waiting to be triggered. Clothes too tight? Itchy legs. Clothes too loose? Itchy legs. A few drips of water on my legs? Itchy legs. A single crumb or grain of sand on the bedsheets? You get it. Just about anything sets them off. In fact, I've gone months at a time without showering, in the past for fear of getting the Ichies. I don't get to go swimming with my family because it's not worth the almost-guaranteed itchiness that'll result.

Once it starts, it tends to get worse and worse, reaching a crescendo of pain and itchiness that at best makes me intolerable to be around. I can't be reasonable when itchy. All I can do is sit and suffer. Generally I'll itch it, and try and find something distracting to do like play a computer game, though sometimes the itchiness makes it impossible to even play a computer game. In the past, it has left me curled up on the ground whimpering. Eventually (after about 45 minutes) it'll start to subside and I'll be able to function again.

This really curtails my options on a day-to-day basis. Not only is it extremely unpleasant, but I feel like I'm missing out on things in life because of it.

When my skin starts to get itchy, I'll often end up picking at particularly itchy spots, often to the point of breaking the skin. I thought I was just getting ingrown hairs on my forearms, biceps and thighs but perhaps it's DH? I have accumulated a fair few scabs that I cannot leave alone and let heal, and have a few pretty visible scars too as a result.

I should mention that I don't really have much of a "rash." Looking at my skin, you'd just see a bunch of scars and sores/scabs - the unhealed ones do sometimes get quite inflamed if I don't leave them alone, but the red inflamed patch of skin would generally be less than 2cm in diameter. I don't get a huge patch of red, just the sores. Which lead me to assume that the sores were due to compulsive picking and that if only I stopped picking and scratching, my skin would LOOK fine (even though it felt itchy).

Anyway, does this sound like it might be caused by celiac disease? It seems like a good fit in that the itchiness is very intense, and that I "scratch the lesions off" (assuming they're lesions). However, I'm not sure if DH ever occurs without a "red patch"?

Any help at all most appreciated. Either way I'm thinking I'll be getting myself a blood test. The only real question is whether to wait to check if my son is diagnosed beforehand or to do it right away before confirming that he actually suffers from celiac disease.

 

 


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



Celiac.com Sponsor (A8-M):



captaincrab55 Collaborator

Sounds like you should visit a Dermatologist.        You could try an Iodine patch test, but it's not accepted as the Gold Standard here n the USA.      I suffered with that itch for over 50 years.

Assumption Newbie

Thanks for the quick reply cc55!

I thought I should probably provide some pics, which I just took now.

back

Open Original Shared Link

arm

Open Original Shared Link

leg

Open Original Shared Link

As you can see there's more scars than actual inflamed areas at the moment.

 

squirmingitch Veteran

I would say you need to get the celiac blood panel. This is it:

Anti-Gliadin (AGA) IgA
Anti-Gliadin (AGA) IgG
Anti-Endomysial (EMA) IgA
Anti-Tissue Transglutaminase (tTG) IgA
Deamidated Gliadin Peptide (DGP) IgA and IgG
Total Serum IgA 


Also can be termed this way:

Endomysial Antibody IgA
Tissue Transglutaminase IgA 
GLIADIN IgG
GLIADIN IgA
Total Serum IgA 
Deamidated Gliadin Peptide (DGP) IgA and IgG

Keep eating a regular gluten diet until all testing is complete. That goes for your son too until he his endoscopy is completed. You need to tell the doc about your son. All 1st degree relatives of celiacs should be tested every 2 yrs even if they have no symptoms. If they do present with symptoms prior to 2 years then they should be tested right away. 

DH presents bilaterally 99% of the time -- appearing on both sides of the body ie: both elbows, both knees, both sides of the back in the same places etc... It is terribly itchy; a bone deep itch, generally worsening (if that's possible) at night, keeping you from sleeping or waking you up. It stings, burns, itches or any combo. It generally does not quit itching in 45 minutes. It itches all the time.

You may or may not have dh. 60% of people with dh test negative on the blood panel. They have to have a dh biopsy of the skin. This is done ADJACENT to NOT ON an active lesion, there is a special staining process. for the biopsy. 

Having said that, celiacs are prone to many skin issues. Your son got the celiac gene from either you, or his mother, or both of you. That does not automatically mean whomever he got the gene(s) from presently has celiac but it's certainly possible and certainly possible that parent will present with celiac at some point in their life. 

A primary care doc can order the celiac blood panel. For that matter, your son's pediatrician could order it for you if he was willing. 

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,171
    • Most Online (within 30 mins)
      7,748

    kyle68j
    Newest Member
    kyle68j
    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

    • DAR girl
      Looking for help sourcing gluten-free products that do not contain potato or corn derived ingredients. I have other autoimmune conditions (Psoriatic Arthritis and Sjogrens) so I’m looking for prepared foods as I have fatigue and cannot devote a lot of time to baking my own treats. 
    • Scott Adams
      I am so sorry you're going through this. It's completely understandable to feel frustrated, stressed, and disregarded after such a long and difficult health journey. It's exhausting to constantly advocate for yourself, especially when you're dealing with so many symptoms and positive diagnoses like SIBO, while still feeling unwell. The fact that you have been diligently following the diet without relief is a clear sign that something else is going on, and your doctors should be investigating other causes or complications, not dismissing your very real suffering. 
    • Oldturdle
      It is just so sad that health care in the United States has come to this.  Health insurance should be available to everyone, not just the healthy or the rich.  My heart goes out to you.  I would not hesitate to have the test and pay for it myself.  My big concern would be how you could keep the results truly private.  I am sure that ultimately, you could not.  A.I. is getting more and more pervasive, and all data is available somewhere.  I don't know if you could give a fake name, or pay for your test with cash.  I certainly would not disclose any positive results on a private insurance application.  As I understand it, for an official diagnosis, an MD needs to review your labs and make the call.  If you end up in the ER, or some other situation, just request a gluten free diet, and say it is because you feel better when you don't eat gluten.      Hang in there, though.  Medicare is not that far away for you, and it will remove a lot of stress from your health care concerns.  You will even be able to "come out of the closet" about being Celiac!
    • plumbago
      Yes, I've posted a few times about two companies: Request a Test and Ulta Labs. Also, pretty much we can all request any test we want (with the possible exception of the N protein Covid test and I'm sure a couple of others) with Lab Corp (or Pixel by Lab Corp) and Quest. I much prefer Lab Corp for their professionalism, ease of service and having it together administratively, at least in DC. And just so you know, Request a Test uses Lab Corp and Quest anyway, while Ulta Labs uses only Quest. Ulta Labs is cheaper than Request a Test, but I am tired of dealing with Quest, so I don't use them so much.
    • Scott Adams
      PS - I think you meant this site, but I don't believe it has been updated in years: http://glutenfreedrugs.com/ so it is best to use: You can search this site for 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/   
×
×
  • Create New...