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

Just diagnosed


Allthatsall

Recommended Posts

Allthatsall Newbie

Hi Everyone, I was just diagnosed about two weeks ago with DH after a 5 yr battle for a diagnosis. As I am just learning, I am hoping someone can help answer a few questions and clarify a few confusions. 

- I have always had IBS since I was in my early 20s. But I am reading that everyone that has DH has celiac. Is this true?  my Dr. Said there are cases of non celiac DH.

- I keep reading about other triggers to avoid besides gluten. What other things should I avoid?

- Why did my Dr tell me to stop taking Aleve? I can't find the answer to this on Google.

- What are the other symptoms of DH besides the rash and itching? There has to be more and I have had a variety of issues that seem to coincide with my rash flares. 

 

Sorry this is so long and thank you in advance.

 


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



Celiac.com Sponsor (A8-M):



squirmingitch Veteran

Welcome to the club you never wanted to be a member of. I'm glad you actually, finally got a diagnosis. 

A dx of dh IS a dx of celiac disease. DH is the skin presentation of celiac disease. NO, there is no such thing as non celiac dh. If you have dh, you have celiac.

Triggers to avoid...... iodine can make the rash flare severely. This does not mean you need to avoid all iodine containing foods b/c we need iodine. You might want to drop the iodized salt & just use plain salt, at least for a while. Eating a lot of shellfish might make your rash flare as shellfish is high in iodine. 

Aleve is an NSAID. NSAID's tend to aggravate the rash so it's best to avoid them unless you really need it. Tylenol seems to be the least offender so if you have to take something, Tylenol would be preferable. 

Allthatsall Newbie

Thank you for your reply. Can you tell me if there are other symptoms associated with DH. I have suffered from migraines for many years as well as some joint issues. Can these things be attributed to DH? Some of what I have read seems to say yes, but there are so few studies out there. Thank you again.  

ravenwoodglass Mentor
4 hours ago, Allthatsall said:

Thank you for your reply. Can you tell me if there are other symptoms associated with DH. I have suffered from migraines for many years as well as some joint issues. Can these things be attributed to DH? Some of what I have read seems to say yes, but there are so few studies out there. Thank you again.  

A diagnosis of DH is a diagnosis of celiac. Migraines and joint pain can also be symptoms of celiac. I haven't had a migraine since I went gluten free but my joint pain took a few months to resolve.  I hope you get some relief soon.

squirmingitch Veteran
5 hours ago, Allthatsall said:

Thank you for your reply. Can you tell me if there are other symptoms associated with DH. I have suffered from migraines for many years as well as some joint issues. Can these things be attributed to DH? Some of what I have read seems to say yes, but there are so few studies out there. Thank you again.  

Since dh is celiac disease, one can have any & all symptoms of celiac disease. I had migraines for 30 years that went away after being gluten-free for a while. Mind screaming pain in bones & joints. Lots of neurological issues. Swelling. Muscle tics. Skin pain & burning. Hot flashes, depression, brain fog -- extreme brain fog!, nausea, vertigo, heart pounding & irregular, anger issues. I could go on & on but the point is that all those things resolved after I was gluten free for a while. 

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,847
    • Most Online (within 30 mins)
      7,748

    rossick11
    Newest Member
    rossick11
    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

    • Colleen H
      Do you or anyone know alot about ibuprofen  I wasn't sure if I was eating too much apple sauce.   Something is making my pain so much worse  I'm referring to the intense pins and needles in my feet and lower legs.  Jaw actually has tardive dystonia and muscle spasms throughout my back Almost like an opposite effect that a pain reliever would do. I'm fairly new to this. Whatever is going on seems to be worsening  Do people get a withdrawal effect from gluten?  It's extremely painful 😖  I'll post that question or research on the site  Thank you everyone for responding 
    • Colleen H
    • Colleen H
      I think I found a huge culprit for severe reactions to create worsening of my c symptoms. Do people with celiac have sensitivity and /or have opposite reaction to certain medications Where can I find a list ?  I'm new here I'm.wondering why I am getting worse when I take certain medicine...the burning feet.  Rebound muscle pain so intense  How many people get opposite effects or have a horrible attack after these meds
    • Colleen H
      Does anyone know if that includes scrambled eggs and healthy smart butter (,gluten free) I add a very tiny amount of margarine less than a teaspoon.  I did no't have any bread    It just seems like no matter what I eat my stomach and nerves over fire and here comes a host of horrible symptoms. My lower abdomen feels horrible, my right leg thigh muscle.. very odd. Jaw pain. Burning feet , joint pain , you name it  The anxiety just creeps up into brain fog. I don't think I could explain this to anyone who is unfamiliar.  Also,  I most likely will not remember posting this until I check it.  This is highly unusual for me because I have an excellent memory.  One weekend before I knew anything about celiac I lost an entire weekend from severe brain fog, confusion, pain, etc.  I honestly thought I was losing my mind. When I think back I recall eating a lot of PBJ sandwiches and turkey sandwiches.  Once again did not know about gluten.  I was just too sick to cook. Do people fast during attacks ?? It seems horrible to keep going through this. I hope I'm not causing my own problems... I wonder if I should fast because I'm not eating gluten .  Chicken ,  scrambled eggs no milk , canned carrots,  gluten free low sugar low fat Greek yogurt which I already posted about 😞 Any suggestions I am open... I am bedridden when this happens to me.  Thank you Celiac community. 🙏🏻❤️      
    • Juliane
      Yeah, that sounds super familiar. When inflammation levels are high — especially at the start of changing your diet — the body often develops a fructose and lactose intolerance. Unfortunately, the only thing that really helps is cutting out anything that isn’t lactose-free or that contains sugar. So basically, stick to meat, veggies, fish…
×
×
  • 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.