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 Celiac.com!
    eNewsletter
    Donate

Dh


ehrin

Recommended Posts

ehrin Explorer

I can't tell if I have DH or Poison Ivy. I'm not allergic to PI so I don't get a severe case. Usually I get a mild rash and it clears up in about a week, and there is hardly any itching. I have raised bumps on the underside of my forearms that are just not clearing up. <_< Granted, I've been gardening every weekend, and there is PI near my garden, but generally this stuff doesn't bother me. It only itches occaisionally, like when I get out of the shower but otherwise it is dormant. So...what does DH look like???

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



Ursa Major Collaborator

Ehrin, here is a link to a site with good images. This link brings you to images of the arms, you can click on the other images to see other parts of the body affected by DH.

Open Original Shared Link

Hope this helps.

Link to comment
Share on other sites
ehrin Explorer

Thanks Ursula - god, that's what it looks like, but it's hardly as itchy as the description says it should be and I've been gluten-free for 6 months now, with no accidental glutenings in the past 3...I just looked at pictures of PI and it certainly doesn't look like that - it's not blisters by any means. Can you have DH and not be itchy???

Link to comment
Share on other sites
Lillyth Explorer
Ehrin, here is a link to a site with good images. This link brings you to images of the arms, you can click on the other images to see other parts of the body affected by DH.

Open Original Shared Link

Hope this helps.

Ursula,

I have a rash on my arms that looks like the one on the guys chest. It doesn't look as bad as any of the others - and it gets redder & itchier after showering. I have been wheat-free since last summer, and the rash showed up after a couple months of consuming low-gluten stuff like spelt & kamut. As soon as I cut out all gluten (within a week) the rash calmed down, but is still mildly there, though rarely itches. The doc I went to see wouldn't test me for DH - gave me some blah-dee-blah about how I obvioulsy have dry skin (I've never had dry skin in my life - nor has anyone in my family). The cream the doc gave me just made it itch WAY worse. Anyway, I am seeing my normal doc this month, but I wanted to beg your wisdom...

Do you think what I have could be DH?

(Yes, I know you're not a doctor, which means that your opinion means 100x more to me)... :D

Link to comment
Share on other sites
Lillyth Explorer
Ursula,

I have a rash on my arms that looks like the one on the guys chest. It doesn't look as bad as any of the others - and it gets redder & itchier after showering. I have been wheat-free since last summer, and the rash showed up after a couple months of consuming low-gluten stuff like spelt & kamut. As soon as I cut out all gluten (within a week) the rash calmed down, but is still mildly there, though rarely itches. The doc I went to see wouldn't test me for DH - gave me some blah-dee-blah about how I obvioulsy have dry skin (I've never had dry skin in my life - nor has anyone in my family). The cream the doc gave me just made it itch WAY worse. Anyway, I am seeing my normal doc this month, but I wanted to beg your wisdom...

Do you think what I have could be DH?

(Yes, I know you're not a doctor, which means that your opinion means 100x more to me)... :D

On second thought - now that I've scrolled down past the first picture under "arms" - it looked exactly like the bottom two. That is, before I went gluten-free & it began to go away... :ph34r:

Link to comment
Share on other sites

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,074
    • Most Online (within 30 mins)
      7,748

    Robert Noah
    Newest Member
    Robert Noah
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Nacina
      Well, that's a big question. When he was seeing the nutrition response testing dr. that changed each time we went in. He hasn't been seeing him regularly for theist ten months. When he had a horribly week in March I started him back on the 4 that were suggested to keep him on. Those are: Standard Process Chlorophyll Complex gluten-free, SP A-F Betafood gluten-free, SP Tuna Omega-3 Oil gluten-free, And Advanced Amino Formula. He also takes a one a day from a company called Forvia (multivitamin and mineral) and Probiotic . Recently he had to start Vitamin D as well as he was deficient.  
    • Fluka66
      Thank you again for your reply and comments which I have read carefully as I appreciate any input at this stage. I'm tending to listen to what my body wants me to do, having been in agony for many years any respite has been welcome and avoiding all wheat and lactose has thankfully brought this.  When in pain before I was seen by a number of gynacologists as I had 22 fibroids and had an operation 13 years ago to shrink them . However the pain remained and intensified to the point over the years where I began passing out. I was in and out of a&e during covid when waiting rooms where empty. My present diet is the only thing that's given me any hope for the future. As I say I had never heard of celiac disease before starting so I guess had this not come up in a conversation I would just have carried on. It was the swollen lymph node that sent me to a boots pharmacist who immediately sent me to a&e where a Dr asked questions prescribed antibiotics and then back to my GP. I'm now waiting for my hospital appointment . Hope this answers your question. I found out more about the disease because I googled something I wouldn't normally do, it did shed light on the disease but I also read some things that this disease can do. On good days I actually hope I haven't got this but on further investigation my mother's side of the family all Celtic have had various problems 're stomach pain my poor grandmother cried in pain as did her sister whilst two of her brother's survived WW2 but died from ulcers put down to stress of fighting.  Wishing you well with your recovery.  Many thanks  
    • knitty kitty
      Welcome to the forum, @Nacina, What supplements is your son taking?
    • knitty kitty
      @BluegrassCeliac, I'm agreeing.  It's a good thing taking magnesium. And B vitamins. Magnesium and Thiamine work together.  If you supplement the B vitamins which include Thiamine, but don't have sufficient magnesium, Thiamine won't work well.  If you take Magnesium, but not Thiamine, magnesium won't work as well by itself. Hydrochlorothiazide HCTZ is a sulfonamide drug, a sulfa drug.  So are proton pump inhibitors PPIs, and SSRIs. High dose Thiamine is used to resolve cytokine storms.  High dose Thiamine was used in patients having cytokine storms in Covid infections.  Magnesium supplementation also improves cytokine storms, and was also used during Covid. How's your Vitamin D? References: Thiamine and magnesium deficiencies: keys to disease https://pubmed.ncbi.nlm.nih.gov/25542071/ Hiding in Plain Sight: Modern Thiamine Deficiency https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533683/ The Effect of a High-Dose Vitamin B Multivitamin Supplement on the Relationship between Brain Metabolism and Blood Biomarkers of Oxidative Stress: A Randomized Control Trial https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316433/ High‐dose Vitamin B6 supplementation reduces anxiety and strengthens visual surround suppression https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9787829/ Repurposing Treatment of Wernicke-Korsakoff Syndrome for Th-17 Cell Immune Storm Syndrome and Neurological Symptoms in COVID-19: Thiamine Efficacy and Safety, In-Vitro Evidence and Pharmacokinetic Profile https://pubmed.ncbi.nlm.nih.gov/33737877/ Higher Intake of Dietary Magnesium Is Inversely Associated With COVID-19 Severity and Symptoms in Hospitalized Patients: A Cross-Sectional Study https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132593/ Magnesium and Vitamin D Deficiency as a Potential Cause of Immune Dysfunction, Cytokine Storm and Disseminated Intravascular Coagulation in covid-19 patients https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7861592/ Sulfonamide Hypersensitivity https://pubmed.ncbi.nlm.nih.gov/31495421/
    • BluegrassCeliac
      Hi,   Not saying Thiamine (B1) couldn't be an issue as well, but Mg was definitely the cause of my problems. It's the only thing that worked. I supplemented with B vitamins, but that didn't change anything, in fact they made me sick. Mg stopped all my muscle pain (HCTZ) within a few months and fixed all the intestinal problems HCTZ caused as well. Mom has an allergy to some sulfa drugs (IgG Celiac too), but I don't think I've ever taken them. Mg boosted my energy as well. It solved a lot of problems. I take 1000mg MgO a day with no problems. I boost absorption with Vitamin D. Some people can't take MgO,  like mom, she takes Mg Glycinate. It's one of those things that someone has try and find the right form for themselves. Everyone's different. Mg deficiency can cause anxiety and is a treatment for it. A pharmacist gave me a list of drugs years ago that cause Mg deficiency: PPIs, H2 bockers, HCTZ, some beta blockers (metoprolol which I've taken -- horrible side effects), some anti-anxiety meds too were on it. I posted because I saw he was an IgG celiac. He's the first one I've seen in 20 years, other than my family. We're rare. All the celiacs I've met are IgA. Finding healthcare is a nightmare. Just trying to help. B  
×
×
  • Create New...