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

Secondary Food Intolerance Caused By Gluten


krishna

Recommended Posts

krishna Apprentice

I was wondering if you guys have any secondary intolerance too apart from gluten and how long did it take to resolve the secondary intolerance? Do you have more than one secondary food intolerance?

Thanks!


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



Celiac.com Sponsor (A8-M):



eatmeat4good Enthusiast

Yes, I found out I cannot tolerate soy about 4 weeks after going gluten free. Dairy also. I don't know how long before they resolve, but for now I have to avoid them.

Nightshades, dairy, soy, are a few of the common secondary intolerances. If you look at the signature lines you will see a lot of intolerances listed by the Celiacs here.

Good luck.

mushroom Proficient

I had problems with corn and was lactose intolerant before I discovered my gluten intolerance (really, I just stopped eating gluten to try to help my arthritis :blink: , not realizing it would help so many other things (but not my arthritis :( )

Since then I have discovered I cannot eat soy, nightshades, citrus, and legumes. Some of these may be temporary intolerances and I may be able to resume eating them once my gut is properly healed.

Pac Apprentice

I became intolerant to rice, probably during the last few years before diagnosis. I've found out just two months ago. I used to be a rice lover until few year ago. Then I started disliking it the same way I always disliked wheat and rye. About the same time I also stopped liking oats. Never tried gluten-free oats, I would probably react to them as well.

Other "intolerances" were not real intolerances, just a side effect of my ruined health. The first few months I could only eat a little bit of meat, milk (especially the sweetened condensed milk), cream, sour cream, fresh cheeses and dried cranberries. I slowly added leafy veggies, other veggies, fresh fruit, seeds. In six months I was able to tolerate small amounts of corn and legumes again. In a year I was able to add potatoes to my regular diet. For long time I couldn't tolerate yogurts but last week I had one and no reaction. I tried another one yesterday and still no reaction. Maybe I'll be able to tolerate yogurt again.

wheeleezdryver Community Regular

When I finally went totally gluten-free last Aug (I was gluten- lite for a while before that), I also realized I was having problems w/ dairy. About 3 weeks ago I started trying cheese & yogurt, and I have no problems with them. Still can't do milk or ice cream w/ o a Lactaid pill, though-- and even then I can't have too much.

I am also trying to figure out fructose intolerance-- I know for sure brown rice (amongst other things) gives me problems, which makes things fun b/c so many gluten-free items have brown rice in them.

cassP Contributor

sometimes dairy

fructose/fructans (hoping this is temporary)

corn

potatoes

too much starch or complex carbohydrates

coffee & tea in excess

sugar in excess

legumes

**these are additional intolerances- had them before going gluten free and after- and i dont think all intolerances are necessarily related to gluten

krishna Apprentice

Thanks everyone.. the most worrying symptom I have is chest tightness and anxiety attacks after eating food (sometimes). I still have random bouts of headaches, constipation is better since I'm taking Trifala (herbal medicine given by my doctor). I'm also taking some digestive enzymes. I think I'm having secondary food intolerance symptoms. I've narrowed it to yeast (maybe) or in general starches/carbohydrates or fatty foods. The way I'm looking at this is that my body is healing and is unable to break down certain foods to absorb completely. Those unbroken/undigested foods enter the blood stream and intoxicate the brain via leaky gut syndrome causing my symptoms. Another explanation is shortage of enzymes to break down other foods (apart from gluten) temporarily but not sure which ones! This also related to what I mentioned about leaky gut syndrome.


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



Celiac.com Sponsor (A8-M):



jerseyangel Proficient

I'm still unable to tolerate coconut, tapioca, legumes, and soy.

I was intolerant to dairy and corn but have been able to reintroduce them successfully. Dairy after 6 years, corn after about 3. I'm still careful not to over-do it with the corn.

cahill Collaborator

I was wondering if you guys have any secondary intolerance too apart from gluten and how long did it take to resolve the secondary intolerance? Do you have more than one secondary food intolerance?

Thanks!

Yes I have secondary intolerances and I am still discovering them. I am not sure that i would even try to reintroduce soy,nightshades or corn into my diet.My reaction to them is so incapacitating.

When I am done with my elimination diet I plan to go grain free again.Dairy is one I am up in the air about,,maybe yes maybe no.

cassP Contributor

Thanks everyone.. the most worrying symptom I have is chest tightness and anxiety attacks after eating food (sometimes). I still have random bouts of headaches,

fyi- i just had left over gluten free chipotle- and even tho i usually avoid corn- i cheated and baked some gluten free corn tortilla chips with cheese to go with my food- and OY VEY- had a little HBP & tachycardia before i even finished my meal :(

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. - trents replied to Ginger38's topic in Related Issues & Disorders
      1

      Shingles - Could It Be Related to Gluten/ Celiac

    2. - Ginger38 posted a topic in Related Issues & Disorders
      1

      Shingles - Could It Be Related to Gluten/ Celiac

    3. - Russ H commented on Scott Adams's article in Latest Research
      5

      Study Estimates the Costs of Delayed Celiac Disease Diagnosis (+Video)

    4. - Russ H posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      Coeliac UK Research Conference 2025

    5. - Rejoicephd replied to Rejoicephd's topic in Related Issues & Disorders
      5

      Basic metabolic panel results - more flags


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,376
    • Most Online (within 30 mins)
      7,748

    Citydweller
    Newest Member
    Citydweller
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      I don't know of a connection. Lots of people who don't have celiac disease/gluten issues get shingles.
    • Ginger38
      I’m 43, just newly diagnosed with a horrible case of shingles last week . They are all over my face , around my eye, ear , all in my scalp. Lymph nodes are a mess. Ear is a mess. My eye is hurting and sensitive. Pain has been a 10/10+ daily. Taking Motrin and Tylenol around the clock. I AM MISERABLE. The pain is unrelenting. I just want to cry.   But Developing shingles has me a bit concerned about my immune system which also has me wondering about celiac and if there’s a connection to celiac / gluten and shingles; particularly since I haven't been 💯 gluten free because of all the confusing test results and doctors advice etc., is there a connection here? I’ve never had shingles and the gluten/ celiac  roller coaster has been ongoing for a while but I’ve had gluten off and on the last year bc of all the confusion  
    • Russ H
      There were some interesting talks, particularly Prof Ludvig Stollid's talk on therapeutics for coeliac disease.    https://www.youtube.com/playlist?list=PLRcl2mPE0WdigRtJPvylUJbkCx263KF_t
    • Rejoicephd
      Thank you @trents for letting me know you experience something similar thanks @knitty kitty for your response and resources.  I will be following up with my doctor about these results and I’ll read the articles you sent. Thanks - I really appreciate you all.
    • knitty kitty
      You're right, doctors usually only test Vitamin D and B12.  Both are really important, but they're not good indicators of deficiencies in the other B vitamins.  Our bodies are able to store Vitamin B12 and Vitamin D in the liver for up to a year or longer.  The other B vitamins can only be stored for much shorter periods of time.  Pyridoxine B 6 can be stored for several months, but the others only a month or two at the longest.  Thiamine stores can be depleted in as little as three days.  There's no correlation between B12 levels and the other B vitamins' levels.  Blood tests can't measure the amount of vitamins stored inside cells where they are used.  There's disagreement as to what optimal vitamin levels are.  The Recommended Daily Allowance is based on the minimum daily amount needed to prevent disease set back in the forties when people ate a totally different diet and gruesome experiments were done on people.  Folate  requirements had to be updated in the nineties after spina bifida increased and synthetic folic acid was mandated to be added to grain products.  Vitamin D requirements have been updated only in the past few years.   Doctors aren't required to take as many hours of nutritional education as in the past.  They're educated in learning institutions funded by pharmaceutical corporations.  Natural substances like vitamins can't be patented, so there's more money to be made prescribing pharmaceuticals than vitamins.   Also, look into the Autoimmune Protocol Diet, developed by Dr. Sarah Ballantyne, a Celiac herself.  Her book The Paleo Approach has been most helpful to me.  You're very welcome.  I'm glad I can help you around some stumbling blocks while on this journey.    Keep me posted on your progress!  Best wishes! P.S.  interesting reading: Thiamine, gastrointestinal beriberi and acetylcholine signaling https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/
×
×
  • 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.