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

Hives, Anyone?

bnsnewman

Recommended Posts

bnsnewman Rookie
bnsnewman
Posted

We have been working really hard at being gluten free for a couple of weeks now. My daughter (she will be 6 in July) has been pretty resistent to the new changes, but she does see what happens when she eats something with gluten in it.

She broke out in hives yesterday, and we have been up since 4 am because she started itching in her sleep and it woke her up. I am giving her Benadryl and using Caladryl as well. She is not running a fever, but she started wheezing a bit when she went to bed last night.

Is this a common reaction to getting off the gluten, or trying new gluten-free foods, or just a random occurance? Has anyone had any similar experiences with their children?

Oh, as a side note, I talked to the assistant principal at school on Friday, and she told me that the school district told her that kindergarten doesn't have the same requirement for a specific number of hours as the other grades do. And the bottom line is, my daughter will not be held back for next year! I almost cried with relief when she told me that. She did say though that next year we will have to fill out the papers for the plan 504, but told me again, they don't have many guidelines for dealing with this. Sigh. At least it's a start.

Natalie

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

Celiac.com Sponsor (A8-M):


dally099 Contributor
dally099
Posted

hi there, does she have hives or DH. i get hives as im allergic to soy, maybe she has some other intolerances now brought on by the celiac, there are some people here that know more about how that happens then i do. but it sounds like allergies to me. i have a special cream made up from my doc that has menthol in it so its cooling at the same time, works well. good luck i know how awful hives can be believe me!!

Teacher1958 Apprentice
Teacher1958
Posted

Hi,

I've been wandering about this for months! I started getting the hives in the fall, shortly before I was diagnosed with fibromyalgia. My doctor said that it was part of the fibromyalgia, which didn't make a whole lot of sense to me. I think she should have further investigated that symptom. Anyhow, my hives take the form of welts that look like I've been slapped with a leather belt or something. I have only gotten them on my tummy and breasts. I've never seen them anywhere else. I have only gotten them once since going gluten free.

Hope this helps.

Ursa Major Collaborator
Ursa Major
Posted

Hives are an allergic reaction to something. I get hives when I eat grains with fruit (everywhere, but I shouldn't eat those anyway). Once I got terrible hives from using a lotion that contained oat bran and apple pectin. I had rubbed it all over my arms, and within seconds they felt like they were on fire, and the hives started. Within 15 minutes my arms were bright red and swollen, covered in one huge hive, despite the fact that I tried to wash off the lotion with soap and water within seconds of applying it.

Are you feeding your daughter a lot of replacement foods for the gluteny things she ate before? A lot of those contain soy, tapioca, rice flour............ things you don't necessarily find in your regular bread/cookies/pasta. If she's only had those hives since starting the gluten-free diet, it must be something she is eating now that she didn't eat before.

You might want to keep a food diary. Write down everything she eats, and when she eats it. Then, when she gets hives, you might be able to track the reaction to a specific food she has eaten.

Teacher1958 Apprentice
Teacher1958
Posted
Hives are an allergic reaction to something. I get hives when I eat grains with fruit (everywhere, but I shouldn't eat those anyway). Once I got terrible hives from using a lotion that contained oat bran and apple pectin. I had rubbed it all over my arms, and within seconds they felt like they were on fire, and the hives started. Within 15 minutes my arms were bright red and swollen, covered in one huge hive, despite the fact that I tried to wash off the lotion with soap and water within seconds of applying it.

Are you feeding your daughter a lot of replacement foods for the gluteny things she ate before? A lot of those contain soy, tapioca, rice flour............ things you don't necessarily find in your regular bread/cookies/pasta. If she's only had those hives since starting the gluten-free diet, it must be something she is eating now that she didn't eat before.

You might want to keep a food diary. Write down everything she eats, and when she eats it. Then, when she gets hives, you might be able to track the reaction to a specific food she has eaten.

---------------------------------------------------

You reminded me of the time one of my students gave me a rose milk lotion for Christmas. I had no idea I was allergic to it, so I lathered it all over my body....groan....and I got hives all over my body.

Belinda Meeker Apprentice
Belinda Meeker
Posted
We have been working really hard at being gluten free for a couple of weeks now. My daughter (she will be 6 in July) has been pretty resistent to the new changes, but she does see what happens when she eats something with gluten in it.

She broke out in hives yesterday, and we have been up since 4 am because she started itching in her sleep and it woke her up. I am giving her Benadryl and using Caladryl as well. She is not running a fever, but she started wheezing a bit when she went to bed last night.

Is this a common reaction to getting off the gluten, or trying new gluten-free foods, or just a random occurance? Has anyone had any similar experiences with their children?

Oh, as a side note, I talked to the assistant principal at school on Friday, and she told me that the school district told her that kindergarten doesn't have the same requirement for a specific number of hours as the other grades do. And the bottom line is, my daughter will not be held back for next year! I almost cried with relief when she told me that. She did say though that next year we will have to fill out the papers for the plan 504, but told me again, they don't have many guidelines for dealing with this. Sigh. At least it's a start.

Natalie

YES I do get them daily also....but still being tested so can't help u much but i do have a suggestion of soemthing to put on them (ppl don't laugh it really works)

I was at my mom-in-laws and she had no Benadryl so she told me to go put some of her Vagicaine Cream on my hives and they stopped itching immed. so maybe try this on ur lil one.

Mybe she got cross tamination some how or lik eothers said something else is making her break out Ima allergic to Lytex too bedides everyting else.

Good luck I hope u find the coulprate :/

Archived

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

Go to topic listing
  • Celiac.com Sponsor (A19):


  • Member Statistics

    • Total Members
      129,970
    • Most Online (within 30 mins)
      7,748
    MJK48
    Newest Member
    MJK48
    Joined
  • Celiac.com Sponsor (A20):

  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m
  • Celiac.com Sponsor (A22):



  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • Wheatwacked
      Newly diagnosed, struggling

      By Wheatwacked · Posted

      Hello @CeliacNew, If you are Vegan to help you feel better, reconsider returning to omnivore.  Actually, since you are already on a very restrictive diet, transitioning to gluten free might be easier for you.  Read the ingredient labels, Particularly vitamin D and Choline require supplements for vegan diet because our primary source is sun, eggs and beef.  B12 also.
    • Wheatwacked
      Multiple symptoms and mixed provider responses

      By Wheatwacked · Posted

      Once you've completed testing and still don't have improvement, start a trial gluten free diet.  Looking for imprvement that may indicate Non Celiac Gluten Sensitivity, which is 10 times more prevalent than Celiac Disease. Deficiencies in vitamins B6, B12, D, and C can manifest as skin rashes.  Virtual guaranty you are deficient in vitamin D.
    • cameo674
      Help vetting HLA-DQ typing provider

      By cameo674 · Posted

      So those rs numbers tell researchers where the dbSNP is located in a Genome so that other reasearchers or an AI system can look in that specific spot for that Snip of information.  You can look those rs # s by pasting the numbers after rs into the lookup on this page https://www.ncbi.nlm.nih.gov/snp/ right under the Blue header bar at the top of the webpage.  Since you are not a researcher, I do not know how this will help you though.
    • cameo674
      Finally got in to doctor to get my referral and I lucked out and got into Gastro the same day - question about different transglutaminase results

      By cameo674 · Posted

      So I posted here once before, and everyone advocated that I get into a GI doc.  I finally got into my functional health appointment on 6/16 to get my blood results evaluated and get the Gastro referral. I was told that I would be fortunate to see a gastro doctor by December, because of the number of people waiting to get in, but they did believe that I needed to see a GI doc among others.  Well, the stars aligned. I got home. I looked at MyChart and it showed an appointment available for later that same day. I never clicked so fast on an appointment time. The gastro doc ran some additional blood work based off the December values that had confirmed my daughter's suspicion that I have undiagnosed stomach issues.  Gastro has also scheduled me to get an upper endoscopy as well as a colonoscopy since it has been 8 years since my last one. She said it would rule out other concerns if I did not show Celiac per the biopsies.  Those biopsies will not occur until August 29th and like everyone here stated, Gastro wants me to keep gluten in my diet exactly as everyone suggested. To be honest, I was barely eating any gluten since I figured I would have plenty of time to do so before testing.  Doc is also looking for the cause of the low level heartburn that I have had for 30 years.  I have mentioned the heartburn to PCPs in the past and they always said take a tums or other OTC drug.  The upper endoscopy is for ruling out eosinphilic esophagitis, h. pylori, and to biopsy the duodenal bulb and second portion to confirm or exclude celiac. The colonoscopy will have random biopsies to rule out microscopic colitis. I didn't really catch her reasoning for the bloodwork.  Doc looked at the December numbers and said they were definitely concerning for Celiac.  She also said, “Hmm that’s odd; usually it’s the reverse”, but I did not catch which result made her say that. She seems very through.  She also asked why I had never bothered to see a GI before.  To be honest, I told her I just assumed that the heartburn and loose stool were a part of aging.  I have been gassy since I was born and thought constantly passing gas was normal?  Everyone I know with Celiac have horrible symptoms that cannot be attributed to other things.  They are in a lot of stomach pain.  I do not go through that.  I attribute my issues to the lactose intolerance that comes with aging, but have slowly been eliminating foods from my diet due to the heartburn or due my assumption that they did not agree with a medication that I was prescribed. I have already eliminated milk products especially high fat ones like ice cream; fats like peanut butter; acids like citrus and tomatoes; chocolate in all forms; and breads more because it is so hard to get in 100 grams of protein if I eat any foods that are not a protein.  I would not have even done the testing if my daughter had not brought up the fact that she thought I might have an undiagnosed condition since she has issues with bloating and another sibling has periodic undiagnosed stomach pain that GI docs throw pills at instead of helping.  Who knew that Bristol scale 5 and 6 were not considered normal especially multiple times a day? I watched my MIL go through basically the same bowel changes starting at 50 so to be honest, I really did think it was normal before this week's appointment.   December 2024's blood tests ran through Quest Labs were:  Deamidated Gliadin (IgA) 53.8 U/mL Above range >15.0 U/mL; Deamidated Gliadin (IgG) >250.0 U/mL Above Range >15.0 U/mL; Tissue Transglutaminase (IgA) 44.0 U/mL Above range >15.0 U/mL; Tissue Transglutaminase (IgG) <1.0 In range <15.0; Immunoglobulin A (IgA) 274 mg/dL In range 47-310 mg/dL 6/16/25 bloodwork:  Until today, I did not really know what all the four tubes of blood were for and since I did not understand the results, I got into the clinical notes to see what was ordered, but it did not exactly explain why for everything. Immunoglobulins IGG, IGA, IGM all came back in range:  IGG 1,010 mg/dL In range 600-1,714; IgA 261 mg/dL In range 66-433 mg/dL; IGM 189 mg/dL In range 45-281.  How do these numbers help with diagnosis? Google says she checked these to see if I have an ongoing infection? I do have Hashimoto's and she did say once you have one autoimmune disease others seem to follow. Celiac Associated HLD-DQ Typing: DQA1* Value: 05; DQA1*DQA11 Value: 05; DQB1* Value: 02; DQB1-DQB11 Value: 02; Celiac Gene Pairs Present Value: Yes; Celiac HLA Interpretation Value: These genes are permissive for celiac disease.  However, these genes can also be present in the normal population. Testing performed by SSOP.  So google failed me.  I think these results basically say I have genes, but everybody has these genes so this test was just to confirm that there is a vague possibility?  Maybe this test result explains why I do not have the horrible symptoms most individuals with celiac have?  I told the GI my assumption is that I am just gluten intolerant since I do not have the pain? So maybe this test explains why I have antibodies? Comprehensive Metabolic Panel: Everything was in the middle of the normal range.  Google says this just says I am metabolically healthy. Tissue Transglutaminase ABS test results – Done by the Mayo Clinic’s Labs –  T-Transglutaminase IGA AB --Value: 3.1 U/mL – Normal Value is <4.0 (negative) U/mL; Tissue Transglutaminase, IgG -- Value: 15.3 U/mL High -- Normal Value is <6.0 (Negative) U/mL – Interpretation Positive (>9.0) – These are the only labs the GI did that have been labeled Abnormal.  I am confused at how/why these came back different than the December labs? Because these numbers seem to be the opposite of what the were in December and I know I have eaten less gluten.  They were definitely measured differently and had different ranges. This must be why she said they are usually opposite? Molecular Stool Parasite Panel said I was Negative for Giardia Lamblia by PCR; Entamoeba Histolytica by PCR and Cryptosporidium Parvum/Hominis by PCR.  So at least I do not need to do a parasite cleanse like everyone on TikTok seems to be doing. So I guess, I am just really asking why the Tissue Transglutaminase numbers are different.  Was it because they were truly different tests? Is it because I have not consumed the crazy amount of gluten one is suppose to eat prior to testing? To be honest, I thought that was only for the biopsy testing. I generally only eat twice a day, and the thought of eating the equivalent of 6 slices of bread is daunting. Even in my youth, I probably only consumed the equivalent of maybe 3 slices a day. Like I said before, now I usually focus on trying to eat 60 gram of protein.  I am suppose to consume 100 grams, but have failed to succeed. I will focus on eating gluten starting in July now that I know my procedure date.
    • Scott Adams
      Worried about being isolated

      By Scott Adams · Posted

      I agree with @trents and wiping down the spot you eat your lunch, and eating the food your brought from home should be safe for even sensitive celiacs. Gluten can jump on your food, so it would likely better better for you to continue eating where you prefer.
×
×
  • Create New...