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

Trigger foods


Jlewisrn

Recommended Posts

Jlewisrn Contributor

When I went to the dr he suggested I go on a histamine restricted diet until we figure out exactly what's going on. He gave me a printout on the foods to avoid and I did some research. It seem a lot of the foods are triggers for some of your DH. Anyway, may be something to look into if you aren't sure what's triggering it or why. It's pretty interesting and it's more common to have a histamine intolerance if you have celiac because of the compromised gut. From what I read anyway


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



Celiac.com Sponsor (A8-M):



Ennis-TX Grand Master

True I found I had a medium histamine tolerance, I just stick to eating one higher histamine food a meal and I am alright, in my case its a bit of stuffy ness and a bunch of mucus forms in my stomach that I puke up. So I avoid OVERLY ripe tomatoes, vingars, a d a few others. Histamine is a very odd things in that it depends on how the food is processed. I found cocoa nibs raw, raw cocoa, and ground nibs from Criobru do not bother me in the least. But processed cocoa and chocolate has to be eaten alone in small amounts. This is due to the fermentation process used to make the processed stuff. I also found black tea to be a huge trigger, and a few others......sorta funny how this works. Also found nothing can be left in my fridge after cooking longer then a few days or it starts making me sick. I have to can stuff quick or freeze it, and eat on something til it is gone no waiting til later in the week. I also found I have to roast nuts and seeds myself at a lower temperature, seems everything else has bee roasted too long ago and makes me feel done and sluggish....sorta funny.

Overall MY best suggestion for anything is keep a food diary, record everything you eat and how it is fixed and with what seasonings, Find those triggers, try them by themselves, then experiment with them seeing if it might be that brand, or how it was prepared, even try getting it as raw and natural as possible to see what the root trigger is. I found the experiments quite enlightening, and very intriguing.

cyclinglady Grand Master

The histamine diet might help.  It certainly will not harm you.  I was on a modified version of it when I had chronic hives for five months.  I suspect a celiac flare-up triggered it over an illness (had flu, cold, tooth infection) and it seems to be related to a damaged gut. I was prescribed a cocktail of anti-histamines which worked.  You would think though that your rash would respond to anti-histamines, if the histamine diet is supposed to help.  

My hives (hundreds of them) would appear daily, like clockwork, every afternoon.  Started off with abdominal pain, an itchy head and then the hives would appear everywhere on my body.  Even the soles of my feet! By morning, they would be gone -- until the afternoon!   Another  symptom that sometimes occured was low blood pressure.  I would pass out.  Vomiting, swelling,  can occur too.   My hives are also triggered by insects.  One bite and hives are all over my body and not just at the bite site.  So, my allergist thinks it is a Mast Cell or autoimmune issue.   There is much medical can do.  It is managed by anti-histamines (H1 and H2), thankfully!  

I sincerely hope you get relief!  

 

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,545
    • Most Online (within 30 mins)
      7,748

    Jem68
    Newest Member
    Jem68
    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

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.