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

Celiac Blood Tests Negative And Chronic Hives


nicolebeth

Recommended Posts

nicolebeth Apprentice

Hi, I've posted here before about my now (almost) 6yo who had low total IgA, and went on to have a negative endoscopy. He's still little, but it's thought that he's on his own 5th %ile curve (he hasn't dropped off his curve, fortunately).

Anyway, I have had hives since October with some mild lip angioedema as well. When the hives started, I had started eating gluten again more regularly. I should start by saying I have had previous negative blood tests for celiac, but overall a bit more energy without gluten (but I'm not sure how much that has to do with gluten and how much it has to do with a sugar spike from those types of foods).

I continued to eat gluten for a month, had new blood tests (for everything to try and track down the hives). All tests, including the celiac tests, were negative. Normal total IgA, negative Endomysial IgA Ab (titer), and the TTG Ab IgA was <1.3 with a reference range of <4.0. My doctor said this conclusively proves no celiac, and that there are no other tests to run. (I had thought there might be others--IgG--but she said that she did them all. On my blood work, these are the only tests that suggest looking for celiac.

I am hypothyroid on 100 mcg of Levoxyl (I had a post-partum hyperthyroid period around the time the hives started, so I dropped the dose to 75 mcg for a month).

I've been through the forums, and have found some people that have had hives in connection with gluten intolerances. I feel pretty willing to try anything, at this point (I've even consulted a homeopath). I'm on Claritin as a sugar pill (though, placebos are meant to work, right? Not sure that the Claritin does anything). I can't/won't take much else as I'm nursing/taking care of an baby and have to drive around two other kids and don't want to be sleepy on top of sleep-deprived.

I know that many have opted to go off of gluten without any lab confirmation. It feels weird, though, to avoid a food (forever) without any kind of "official" confirmation. Is there any other test to take (aside from an endoscopy)? (I've also been "diagnosed" with IBS; I had a lower GI and barium enema in 1994.) When I was pregnant, I had no obvious problems with gluten, more problems with nightshades (which bother me here and there still). I've been lactose intolerant of most products with lactose for a long time. I don't seem to tolerate simple sugars well. The most recent lip swelling came after "matzah baklava" (gluten + sugar, and a few pistachios) last night. I'm going into my PCP again today (just to be annoying, probably).

What I have read (on About Thyroid) is that there is a strong gluten intolerance connection to hypothyroidism. Also, I've read that the hives could be an autoimmune disorder (with or without a gluten connection).

If anyone has any thoughts about this, I'd appreciate it. I've got a week where it's super-easy to avoid gluten (Passover). And a few days where I can't take Claritin at all (waiting for an allergist appointment next Monday). If it is gluten, how soon would I be able to know this? Compared to some, there's nothing at all wrong with me. Yet, it is beyond annoying to be covered in hives, itchy most evenings, and my 9yo is grossed out (I'm a little grossed out, too).

Thank you!


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



Celiac.com Sponsor (A8-M):



eatmeat4good Enthusiast

Open Original Shared Link

Open Original Shared Link

Interesting you should post this. I have hives too. Salicylic acid intolerance and thyroid disease can contribute to chronic hives. Elimination is the most effective tx. My hives react really bad to benzoates which are in almost all sodas and juice drinks. Food coloring activates them too. Yes, it's hard to get rid of whole food groups without diagnosis, but if the hives go away it is worth it. Had a horrible reaction to M&M's with a diet coke...within 30 min...hives all over my face and angioedema.

I have to avoid Gluten, Salicylates, Benzoates, Tartrazine, Nitrites, Sulfites which means almost all processed foods. I just made the connection myself. Dr. has me avoiding these additives and taking Zyrtec Certrazine twice a day to try to control the hives.

They used to say there was nothing that could be done about chronic hives, but now they are finding it related to food additives and preservatives. I hope it helps you or at least that you find the articles interesting.

nicolebeth Apprentice

Open Original Shared Link

Open Original Shared Link

Interesting you should post this. I have hives too. Salicylic acid intolerance and thyroid disease can contribute to chronic hives. Elimination is the most effective tx. My hives react really bad to benzoates which are in almost all sodas and juice drinks. Food coloring activates them too. Yes, it's hard to get rid of whole food groups without diagnosis, but if the hives go away it is worth it. Had a horrible reaction to M&M's with a diet coke...within 30 min...hives all over my face and angioedema.

I have to avoid Gluten, Salicylates, Benzoates, Tartrazine, Nitrites, Sulfites which means almost all processed foods. I just made the connection myself. Dr. has me avoiding these additives and taking Zyrtec Certrazine twice a day to try to control the hives.

They used to say there was nothing that could be done about chronic hives, but now they are finding it related to food additives and preservatives. I hope it helps you or at least that you find the articles interesting.

Very interesting! Thank you for all that information. I'm getting a new remedy from the homeopath, going on Day 2 of no gluten (my PCP was very much in favor of that, says she sees lots of cases of gluten intolerance that aren't celiac), and have an allergist appointment on Monday. (Sadly, the hives are too bad to cut out the antihistamine, so I hope the appointment isn't a waste on Monday.) Anyway, I appreciate the information about how so much of our diet can contribute to this. This is the second time it has happened to me--the first time, it went away when I was away from home. This time, I still had the hives while on vacation, and it has gone on for much longer (and is more annoying). Anyway, thanks again for your response.

eatmeat4good Enthusiast

I feel for you. I know it is miserable. I use antihistamines too. In fact one of the articles I read said Chronic hives respond best to Certazine morning and night. Though the directions say only take it once a day. I thought you might want to ask your Dr. about that in case you want to try. Zyrtec, Certrazine works better for me than Claritin. I hope you get some relief.

nicolebeth Apprentice

Good tip about the Zyrtec. I was just told to take Claritin back in 2003 (the first time this happened), and I kind of went back to it. It's odd how they seem to be getting worse (and seem to come around 8:30pm every day, regardless of whether I've taken Claritin yet that day or not). The more I've read up on this, the more I doubt the allergist will be able to do anything as long as I'm on any kind of antihistamine. They'd probably rather I take benadryl as it would be out of my system faster. I do so enjoy the two hours or so a day that are hive-free...which I'm guessing is courtesy of the 24-hr drug. Perhaps the allergist can at least do the IgG blood draws for celiac that I didn't have before--I was eating plenty of gluten until a few days ago, so I imagine that will work.

Thanks again!

eatmeat4good Enthusiast

I just have to make another comment. Your symptoms are worse in the evening...after you have been eating gluten during the day. My DH activated in the evenings too. Horrible itching and burning and yet in the mornings I seemed to have some reprieve. If it is DH you should ask for a skin biopsy and have them take it next to the lesion on clear skin. That is where the antibodies are found. I never made the connection about the sores being activated in the evenings, but it no longer happened once I went gluten and iodine free. I sure hope you try eliminating gluten...that could be the cause of it all.

nicolebeth Apprentice

I wondered, too, about the timing. Although, today, the symptoms are pretty bad though tolerable (no gluten, but no Claritin yesterday). I did have a biopsy of the original hive (the derm. thought it was pityriasis rosea, but it wasn't acting like that. Anyway, she biopsied two actual hives, themselves, and they were found to be...hives. I haven't seen any kind of rash that looks any different from hives. So, I wasn't thinking it could be DH, though I've heard that hives + hypothyroidism could mean gluten intolerance (or something like that).


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:
    Join eNewsletter
    Donate

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - catnapt posted a topic in Related Issues & Disorders
      0

      anyone here diagnosed with a PARAthyroid disorder? (NOT the thyroid) the calcium controlling glands

    2. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      how much gluten do I need to eat before blood tests?

    3. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      Curious question

    4. - Amy Barnett posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Question

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,322
    • Most Online (within 30 mins)
      7,748

    avery144
    Newest Member
    avery144
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • catnapt
      learned I had a high PTH level in 2022 suspected to be due to low vit D  got my vit D level up a bit but still have high PTH   I am 70 yrs old (today in fact) I am looking for someone who also has hyperparathyroidism that might be caused by malabsorption    
    • catnapt
      I am on day 13 of eating gluten  and have decided to have the celiac panel done tomorrow instead of Wed. (and instead of extending it a few more weeks) because I am SO incredibly sick. I have almost no appetite and am not able to consume the required daily intake of calcium to try to keep up with the loss of calcium from the high parathyroid hormone and/or the renal calcium leak.    I have spent the past 15 years working hard to improve my health. I lost 50lbs, got off handfuls of medications, lowered my cholesterol to enviable levels, and in spite of having end stage osteoarthritis in both knees, with a good diet and keeping active I have NO pain in those joints- til now.  Almost all of my joints hurt now I feel like someone has repeatedly punched me all over my torso- even my ribs hurt- I have nausea, gas, bloating, headache, mood swings, irritability, horrid flatulence (afraid to leave the house or be in any enclosed spaces with other people- the smell would knock them off their feet) I was so sure that I wanted a firm diagnosis but now- I'm asking myself is THIS worth it? esp over the past 2 yrs I have been feeling better and better the more I adjusted my diet to exclude highly refined grains and processed foods. I didn't purposely avoid gluten, but it just happened that not eating gluten has made me feel better.   I don't know what I would have to gain by getting a definitive diagnosis. I think possibly the only advantage to a DX would be that I could insist on gluten-free foods in settings where I am unable to have access to foods of my choice (hospital, rehab, nursing home)  and maybe having a medical reason to see a dietician?   please let me know if it's reasonable to just go back to the way I was eating.  Actually I do plan to buy certified gluten-free oats as that is the only grain I consume (and really like) so there will be some minor tweaks I hope and pray that I heal quickly from any possible damage that may have been done from 13 days of eating gluten.    
    • Jmartes71
      So I've been dealing with chasing the name celiac because of my body actively dealing with health issues related to celiac though not eating. Diagnosed in 1994 before foods eliminated from diet. After 25 years with former pcp I googled celiac specialist and she wasn't because of what ive been through. I wanted my results to be sent to my pcp but nothing was sent.I have email copies.I did one zoom call with np with team member from celiac specialist in Nov 2025 and she asked me why I wanted to know why I wanted the celiac diagnosis so bad, I sad I don't, its my life and I need revalidaion because its affecting me.KB stated well it shows you are.I asked then why am I going through all this.I was labeled unruly. Its been a celiac circus and medical has caused anxiety and depression no fault to my own other than being born with bad genetics. How is it legal for medical professionals to gaslight patients that are with an ailment coming for help to be downplayed? KB put in my records that she personally spent 120min with me and I think the zoom call was discussing celiac 80 min ONE ZOOM call.SHE is responsible for not explaining to my pcp about celiac disease am I right?
    • Amy Barnett
      What is the best liquid multivitamin for celiac disease?
    • Jmartes71
      I've noticed with my age and menopause my smell for bread gives me severe migraines and I know this.Its alarming that there are all these fabulous bakeries, sandwich places pizza places popping up in confined areas.Just the other day I suffered a migraine after I got done with my mri when a guy with a brown paper bag walk in front of me and I smelled that fresh dough bread with tuna, I got a migraine when we got home.I hate im that sensitive. Its alarming these places are popping up in airports as well.I just saw on the news that the airport ( can't remember which  one)was going to have a fabulous smelling bakery. Not for sensitive celiacs, this can alter their health during their travel which isn't safe. More awareness really NEEDS to be promoted, so much more than just a food consumption!FYI I did write to Stanislaus to let them know my thoughts on the medical field not knowing much about celiac and how it affects one.I also did message my gi the 3 specialist names that was given on previous post on questions on celiac. I pray its not on deaf door.
×
×
  • 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.