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

Possibility Of Food Intolerances? Suggestions Needed!


jamiecasabellameeks

Recommended Posts

jamiecasabellameeks Apprentice

Hi, everyone!! I was diagnosed with Celiac Disease approximately 1 month ago, and I have been gluten free 1 1/2 months! I really do feel a lot better but still not "normal".  I know and understand that it takes a WHILE for your body to heal from all of the damage.  I am trying to be patient, but I really do feel that I have some intolerances to other foods as well (possibly soy, dairy, sugar).  I have been in denial...because well, I felt like I had already given up so much!!  :unsure:

 

I now realize, however, that I just have to do this 100%, regardless, if I want to feel 100% better! I just need advice on the best way to go about it!  Should I go to my GP and ask to be tested for other food intolerances (or do they even do that)?  I must add that I live in Mississippi...The Celiac diagnosis, from my personal experience, is not always well accepted and is thought of as a "fad".  Feel a little lost at times...not knowing where to turn...

 

I don't REALLY want to just cut everything out without actually KNOWING what is causing me to not feel well?? I just want proof, I guess.

 

What are your experience?? I would really like to hear...I have learned more from the stories on this forum than from any doctor or dietician that I have seen!

 

Thanks in advance for your help!!!!!!!


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



Celiac.com Sponsor (A8-M):



shadowicewolf Proficient

You could try removing dairy for a while and see what happens. Some celiacs don't handle dairy very well when they are healing.

kareng Grand Master

Don't you have an actual diagnosis from a doc? If you have a doctor that thinks Celiac isn't real, you should get another doctor.

The best way to see if you are intolerant to a food is an elimination diet and food diary. I think you should give the gluten-free diet a few more months before you try to eliminate most all foods and try them on at a time. Don't eat dairy and gluten-free oats ( if you are eating them) and give it a few months.

jamiecasabellameeks Apprentice

Don't you have an actual diagnosis from a doc? If you have a doctor that thinks Celiac isn't real, you should get another doctor.

The best way to see if you are intolerant to a food is an elimination diet and food diary. I think you should give the gluten-free diet a few more months before you try to eliminate most all foods and try them on at a time. Don't eat dairy and gluten-free oats ( if you are eating them) and give it a few months.

I do have a diagnosis from my GI doc.  My GP is actually the one who referred me for testing, but even he admitted that he didn't know much about it.  I was referred to a dietician.  I felt like I found more on google and was more prepared for the meeting than him.  He has actually only worked with one other Celiac.  My family members (who have symptoms and SHOULD get tested) are hesitant to believe that it's as serious of a condition as I make it out to be...Sad, really, but true.  So, now I feel like I just have to PRETEND to feel better just to not have to listen to anyone saying anything about how I'm overreacting, etc...

 

I guess the weirdest thing about it is...I was feeling SO GOOD last week...so much so that I thought I was "healed".  What changed!?! Why do I feel bad all of a sudden?  This is the most confusing disease, truly.  I mean, I can't figure if I've glutened myself somehow (my kids still eat it) or if I have some other intolerance...

dilettantesteph Collaborator

I read up on testing for food intolerances.  It seemed like the tests are expensive and not very accurate.  You can use them as starting points for challenge/elimination dieting, but you still have to do those diets to be sure of what bothers you.  Your problem may not be other food intolerances anyway.  It may be that you are sensitive to the low levels of gluten allowed in gluten-free foods.  The levels tolerated vary widely.  In any case, it helps to keep a food journal and do challenge/elimination dieting.  Basically, if you think that something bothers you, stop eating it and see what happens.  If you are uncertain, start eating it again and see what happens.  

 

I also felt much better when I first went gluten free and then started having problems again.  I had to learn a lot more about avoiding gluten before I could be completely symptom free.  I hope that you feel better soon.

jamiecasabellameeks Apprentice

I read up on testing for food intolerances.  It seemed like the tests are expensive and not very accurate.  You can use them as starting points for challenge/elimination dieting, but you still have to do those diets to be sure of what bothers you.  Your problem may not be other food intolerances anyway.  It may be that you are sensitive to the low levels of gluten allowed in gluten-free foods.  The levels tolerated vary widely.  In any case, it helps to keep a food journal and do challenge/elimination dieting.  Basically, if you think that something bothers you, stop eating it and see what happens.  If you are uncertain, start eating it again and see what happens.  

 

I also felt much better when I first went gluten free and then started having problems again.  I had to learn a lot more about avoiding gluten before I could be completely symptom free.  I hope that you feel better soon.

Thank you for your comment!  I think at the beginning of this I thought I wouldn't be one of the "sensitive ones"...I'm starting to feel otherwise now.  Like tonight, my husband's family cooked dinner...Of course, I couldn't eat a thing and DIDN'T! BUT...my 3 kids DID! Despite thorough hand-washing and trying to not touch anything, I feel HORRIBLE! I just don't think I can even go over there anymore.  It all seems ridiculous, but I know that's why I'm feeling this way...because I haven't eaten anything! How do you stay away from it completely?? That's what I'm having the hardest time with right now.  I feel like I need cover myself in plastic wrap when I go in public!  So hard to explain that to "non-Celiacs".  That's why I'm so thankful for this forum.  It's at least a little relief to just know you are not alone!

mushroom Proficient

You have to learn to carry safe food with you wherever you go.  Always keep gluten free food in the car, in your purse, and take a meal with you when invited out to eat.  Always make sure your food is on a clean plate or on a paper towel on the counter, just take precautions, cover food you microwave.  You don't have to talk to anybody about it or explain anything to anyone beyond saying that you are intolerant of gluten and cannot eat food prepared by people who dont know how to keep it gluten free.  You can say it is hard enough for you to keep yourself gluten free without expecting someone else to be able to do it for you. :)


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



Celiac.com Sponsor (A8-M):



dilettantesteph Collaborator

I find that it really helps to control gluten intake where I can.  That way if I get some accidental gluten from elsewhere, it doesn't bother me as much.  I have a little bit of wiggle room.  Also, once you are well healed, you don't experience symptoms as easily.  I am not less sensitive at all, unfortunately, but it takes awhile to get re damaged enough to notice it.  I can take a hit from airborne gluten at the farmer's market, for example, and still go on with my life.  It just takes while to figure out your individual level of sensitivity and how to manage it.  There are a lot of ups and downs along the way, but you can get there.

 

I actually don't carry food around with me unless I am going on an overnight trip.  I just don't eat when I'm out.  I'll eat before I go or when I get back.  That's easier and safer for me.

julissa Explorer

after I went gluten free I felt worlds better, but not fully. I was still nauseous and had terrible heartburn at times. I suspected dairy and soy. I tried an elimination diet for those one thing at a time. I then went to an allergist and found out I am allergic to both. so now, knowing that, I am gluten, dairy and soy free, and feel pretty darn great!

 

as far as the other issue, I know how hard that is. just carry your own food if you are going to social situations. it's hard around kids when they are eating. my grandkids always want to hand me their gluteny food with their precious gluteny fingers.

  • 2 weeks later...
Deaminated Marcus Apprentice

Hello Jamie,

 

I felt better after going gluten free but in the following year my fibromyalgia pain returned.

I discovered it was the red kidney beans and later other foods.

Later, I did that expensive food intolerance test and I'm glad I did it because it pointed out other problem foods like peas which I never would have suspected.

But if you don't want to take this test, I recommend cutting out dairy, eggs, oats, and even all beans and peas.

Then reintroduce them one at a time once you feel better.

 

I understand about those dinners.

I wasn't invited to dinner parties after I went gluten free even though I could have eaten the vegetables and meat.

Also no one believed me, because I wasn't skinny.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,025
    • Most Online (within 30 mins)
      7,748

    Amari Love
    Newest Member
    Amari Love
    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

    • Scott Adams
      Your experience is both shocking and critically important for the community to hear, underscoring the terrifying reality that cross-contamination can extend into the most unexpected and invasive medical devices. It is absolutely devastating that you had to endure six months of sickness and ultimately sustain permanent vision loss because a doctor dismissed your legitimate, life-altering condition. Your relentless research and advocacy, from discovering the gluten in MMA acrylic to finding a compassionate prosthodontist, is a testament to your strength in a system that often fails celiac patients. While the scientific and medical consensus is that gluten cannot be absorbed through the skin or eyes (as the molecules are too large to pass through these barriers), your story highlights a terrifying gray area: what about a substance *permanently implanted inside the body*, where it could potentially shed microparticles or cause a localized immune reaction? Your powerful warning about acrylic lenses and the drastic difference with the silicone alternative is invaluable information. Thank you for sharing your harrowing journey and the specific, severe neurological symptoms you endure; it is a stark reminder that celiac is a systemic disease, and your advocacy is undoubtedly saving others from similar trauma.
    • Scott Adams
      Those are driving distance from me--I will try to check them out, thanks for sharing!
    • Scott Adams
      I am so sorry you're going through this bad experience--it's difficult when your own lived reality of cause and effect is dismissed by the very professionals meant to help you. You are absolutely right—your violent physical reactions are not "what you think," but undeniable data points, and it's a form of medical gaslighting to be told otherwise, especially when you have a positive HLA-DQ2 gene and a clear clinical picture. Since your current "celiac specialist" is not addressing the core issue or your related conditions like SIBO and chronic fatigue, it may be time for a strategic pivot. Instead of trying to "reprove" your celiac disease to unwilling ears, consider seeking out a new gastroenterologist or functional medicine doctor, and frame the conversation around managing the complications of a confirmed gluten-free diet for celiac disease. Go in and say, "I have celiac disease, am strictly gluten-free, but I am still suffering from these specific complications: SIBO, chronic fatigue, dermatological issues, and high blood pressure linked to pain. I need a partner to help me address these related conditions." This shifts the focus from a debate about your diagnosis to a collaborative plan for your current suffering, which is the help you truly need and deserve to work toward bouncing back.
    • NanCel
      Hello, no I had to have them re done and then used a liner over the top.  Many dentists are not aware of the celiac effects.  Best of luck.   There is other material, yet, very expensive.
    • sleuth
      He is not just a psychiatrist.  He is also a neuroscientist.  And yes, I have already read those studies.   I agree with benfotiamine.  This is short term while glutened/inflammation occurs.  As I had already mentioned, these symptoms no longer exist when this phase passes.  And yes, I know that celiac is a disease of malnutrition.  We are working with a naturopath.
×
×
  • 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.