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

Desperate - When Does It Get Better?


gbrennan

Recommended Posts

gbrennan Newbie

I am self-diagnosed DH, been gluten free 6 months. I felt like I was getting better, but have been experiencing a terrible outbreak for the past month. Pretty sure I haven't eaten gluten, and have gone dairy free, avoiding iodine. Would love to hear other people's experiences about how long this took.

Almost positive this is DH - can't imagine what else it could be. This is ruining my life.


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



Celiac.com Sponsor (A8-M):



squirmingitch Veteran

gbrennan, Try reading this thread. I was having problems like you are & posted. These good people dissected everything for me & came up with salicylates. Read the thread. It has made a big difference for me.

https://www.celiac.com/forums/topic/91375-upset-confused-venting-scared-frustrated/

IrishHeart Veteran

Excerpted From Celiac Disease: The Hidden Epidemic. Dr. Peter H. R. Green and Rory Jones Chapter 11

..."DH is very erratic. Since the skin may not be rid of IgA deposits for more than 2 years after starting a gluten-free diet, flare- ups occur without obvious gluten ingestion.

It may take patients a substantial amount of time to erase years of IgA buildup in the skin."

A flare could also be due to inadvertent gluten ingestion, iodine, or the use of NSAIDS. Opinions vary as to whether topical lotions and creams have ingredients that might trigger a reaction and stress may exacerbate the flares, although there is no science behind the stress link.

If the patient has DH, it may take years for it to get better. (Green )

I know that some people also report a huge improvement following a low salicylate diet --as Squirmy has suggested.

Hope you feel better soon!

gbrennan Newbie

gbrennan, Try reading this thread. I was having problems like you are & posted. These good people dissected everything for me & came up with salicylates. Read the thread. It has made a big difference for me.

https://www.celiac.com/forums/topic/91375-upset-confused-venting-scared-frustrated/

I just read that coconut milk is high in salicylates - have you had any experience with coconut products? I drink coconut milk and water pretty regularly. Thanks for the link.

squirmingitch Veteran

I haven't tried the coconut milk or water b/c of iodine content which I was avoiding. I did try the coconut oil but then found it's high in sals sooooooo...... Coconut is off my list for the time being. I have some luscious coconut macaroons sitting here that I ordered & they sit unopened.sad.gif

Hang in there.

(((HUGS))))

Di2011 Enthusiast

Sals are big problem for me too. Raisins were my first obvious candidate and then corn became another and both are on the high sals content list. BTW I believe sals effect me in a 'cumulative' way. The more I eat over time the worse the DH gets unlike: Iodine which was a temporary flare trigger in my earlier days but now I can tolerate it in moderation.

ciamarie Rookie

And for me, the biggie I need to avoid is MSG and all of it's related variations (such as 'natural flavors'). See here: Open Original Shared Link

I even recently tried some ground turkey that has 'natural flavors', and guess what? Started itching again... :P I am also somewhat low iodine now too, since I went that route after 2 months of a gluten-free diet and not much progress on the DH. At that point I did have progress on other things like brain fog, etc. so I knew I was getting close. I'm now about a week away from 6 months, and I very rarely have itchiness, and when I do it doesn't last long.


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



Celiac.com Sponsor (A8-M):



Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - wellthatsfun posted a topic in Coping with Celiac Disease
      0

      still struggling with cravings

    2. - RDLiberty replied to RDLiberty's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Toothpaste question.

    3. - RMJ replied to nanny marley's topic in Related Issues & Disorders
      12

      Manitol and mri

    4. - nanny marley replied to nanny marley's topic in Related Issues & Disorders
      12

      Manitol and mri


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,795
    • Most Online (within 30 mins)
      7,748

    susaneschiff
    Newest Member
    susaneschiff
    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

    • wellthatsfun
      as my last post stated, i was diagnosed via endoscopy on the 14th of june. i have been eating amazing home cooked meals, luckily, mainly cooked by my boyfriend who is extremely careful about contamination (and is an incredible cook at that). however, i find myself in a mental rut still. being 18, this is the time in my life where i should be exploring things, going out, having fun. yet every corner i turn i'm tortured by the amazing smell of something i can't have anymore. the wonderful sight of such yummy foods. it's near torture. if my boyfriend and his friend who lives with us buy something i can't have, they'll usually eat it outside of the house or the car or wherever we are - which is greatly appreciated - but even seeing a burger or chips or a sausage roll in their hands guts me almost beyond repair. i just wanna have it again too. i miss it. i feel left out and it makes me very sad all the time. it's not their fault. they are allowed to eat whatever they want to, whatever their intestines will allow. it just stings, bad. and i feel so ungrateful given i basically have a private chef who is doubly the love of my life. but it's just so hard. i know i'll adapt. i haven't given up hope.i just wanted to vent. thank you for reading
    • RDLiberty
      Thank you. I must have misinterpreted a study or something. Thank you for the clarification. Much appreciated. Almost three years into my celiac diagnosis and I'm still learning new things. 
    • RMJ
      I wasn’t clear, glucagon and gadolinium were intravenous. I drank about 5 cups of the prep during 45 minutes. I feel very tired now, probably partly because I was nervous, and partly because I had to fast for 6 hours beforehand and wasn’t very hungry when I got home.
    • nanny marley
      That seems at lot of solution to have put threw you when you already have bowel issues , I will phone them tomorrow because it's sorbitol I have reactions too, thankyou for the input how do you feel now ? I'm not sure I can keep still for that long with my back issues either unfortunately I didn't know it could take that long 😕
    • RMJ
      The solution I had to drink contained sorbitol and mannitol. I was in the MRI, lying on my back, for about 40 minutes. I was given glucagon partway through, and a gadolinium contrast agent. After I got home there was some diarrhea from the prep solution.
×
×
  • 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.