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

Other Food Allergies May Be Appearing?


Palindrome

Recommended Posts

Palindrome Newbie

I was diagnosed with Celiac 8 months ago, and at first I felt MUCH better. Almost all my symptoms went away and I was happy to be able to wake up without pain and be able to do more than lay on the couch all day sick. The past month or so, however, I've been slowly getting sick all over again. I realize that once you go off gluten, you have to give it at least a year until you're healed, but I feel a bit discouraged since I make sure that nothing I put in my mouth has gluten in it. The pains are coming back, along with joint pain, the occasional (painful) digestive issue, and somedays I just feel miserable.

I've been dairy free since diagnosis as well, but I'm thinking it could be a soy or casein allergy? Recently, I seem to be getting sick from anything salty or sugary, and I've been making sure to write down what I eat and the reactions. (Sometimes I get sick, sometimes I don't so I become quite frustrated.) I have gained only a few pounds since going gluten free, and I struggle quite a bit to keep my weight above 100.

I guess my question is does anyone have any idea of what I could be doing wrong or if I do have other food allergies appearing?

(Also, the doctors around here aren't any help. It was a pain to get my GI doctor to even test for Celiac, and when I got my endoscopy/colonoscopy, he focused on testing for Crohn's Disease.)


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



Celiac.com Sponsor (A8-M):



sb2178 Enthusiast

I was put on a fairly strict elimination diet. (am still on it...) Basically, limited foods until you feel fine and then add new ones slowly and keep a detailed journal of what you are eating and how you feel.

Start: Lamb, turkey, rice, millet, cooked carrots, summer squash/zucchini, applesauce, canola oil, and salt. (I also added almonds-- not something I eat regularly but that could be portable snack food. Generally, nuts are out because they are a common problem.)

Added first week: sweet potatoes, canned pears

Second week: dairy, canned pineapple, egg

Third week: Soy, beans or lentils.

And so on... I dropped all meds and supplements for the duration because everything seemed to have corn or soy in it. A nutritionist or decent GI doc should be able to guide you through it. IgG and IgE testing are also options, but how you feel in response to the foods is a bit more reliable. It's a pain, but useful and I've found that I do quite well on lamb, rice, veg, and applesauce even if it's wicked boring.

Good luck.

PrincessHungry Newbie

Similar situation here! I went gluten-free in August and was super excited when I started feeling better. Then around November, everything went crazy. It was like everything was making me sick. I started cutting foods out and noticed things that made it worse but not better. I have been down to so little, I've lost a lot of weight and still have no clue. Something I have noticed about the elimination diet though...don't count out foods unless you've TRIED them. For example, I ate brown rice and was soooo sick. I figured all rice was out but white rice is pretty good. Brown rice made me feel like I was going to vomit at any second. Now I live on white rice. Don't assume anything.

Good luck, let me know if anything works.

PS, I feel your doctor frustrations. I'm always tempted to call my first GI doctor just to tell him to go to hell. He basically laughed in my face. Won't be going back to him, ever!

luvs2eat Collaborator

I've been gluten free for 9 years. Now I've come to the undeniable conclusion that dairy's the thing that's been giving me new and different problems for months! Believe it or not... I'm finding going dairy free much harder than going gluten free!

  • 5 weeks later...
T.H. Community Regular

Just saw you were searching for answers and figured I'd ask: have you looked at (dietary) fructose malabsorption? The rice thing made me think of it, as brown rice is bad for people with this issue, and white rice seems to be okay. Involves fruits and veggies and grains, so it can cover a lot of foods!

This site talks about some of the foods that are good and bad, if you care to take a look:

Open Original Shared Link

Similar situation here! I went gluten-free in August and was super excited when I started feeling better. Then around November, everything went crazy. It was like everything was making me sick. I started cutting foods out and noticed things that made it worse but not better. I have been down to so little, I've lost a lot of weight and still have no clue. Something I have noticed about the elimination diet though...don't count out foods unless you've TRIED them. For example, I ate brown rice and was soooo sick. I figured all rice was out but white rice is pretty good. Brown rice made me feel like I was going to vomit at any second. Now I live on white rice. Don't assume anything.

Good luck, let me know if anything works.

PS, I feel your doctor frustrations. I'm always tempted to call my first GI doctor just to tell him to go to hell. He basically laughed in my face. Won't be going back to him, ever!

T.H. Community Regular

Some quick ideas:

- genetically modified foods seem to cause an increase in allergies to OTHER foods in animal studies. My GI is starting to see this in his auto-immune patients, too, so he recommends eating everything organic.

- if you try the elimination diet, I would dump the 8 most common allergens, everything in the grass family, and then do a bit of research on corn allergies, too. And actually...the grass family issue? That would pretty much cover 'salty and sugary.' Sugarcane is in the grass family along with corn, and corn is in everything, from ALL iodized salt to baking powder to a dusting between paper plates. It's VERY hard to avoid. I mention it because I was reacting to more and more as well, and it didn't stop until I managed to avoid all the foods that were 'bad' for me, completely. I notice now that if I start getting something that I'm reacting to, all the other reactions start getting worse as well, and I'll react to things that didn't bother me before. So I think it's definitely possible that you are reacting to something in the diet.

- for an elimination diet, my dietician gave me this advice: record down brand names of everything you try, as well. You never know what company might have something contaminated by something else, use a certain pesticide, etc... Also, if you stick to the same food for, say, 2-3 days, and then switch to another set that doesn't have ANY of the same ones, and then switch back, you might be able to notice a pattern better between reactions and foods. Since some reactions can be delayed up to 48 hours, I think the 2-3 days to stay on one food might be useful to get a better handle on things.

- you might also wanna check out fructose malabsorption ( Open Original Shared Link ) and sulfite allergies. Those both involve a wide range of foods, so that might apply in your case. :-)

I was diagnosed with Celiac 8 months ago, and at first I felt MUCH better. Almost all my symptoms went away and I was happy to be able to wake up without pain and be able to do more than lay on the couch all day sick. The past month or so, however, I've been slowly getting sick all over again. I realize that once you go off gluten, you have to give it at least a year until you're healed, but I feel a bit discouraged since I make sure that nothing I put in my mouth has gluten in it. The pains are coming back, along with joint pain, the occasional (painful) digestive issue, and somedays I just feel miserable.

I've been dairy free since diagnosis as well, but I'm thinking it could be a soy or casein allergy? Recently, I seem to be getting sick from anything salty or sugary, and I've been making sure to write down what I eat and the reactions. (Sometimes I get sick, sometimes I don't so I become quite frustrated.) I have gained only a few pounds since going gluten free, and I struggle quite a bit to keep my weight above 100.

I guess my question is does anyone have any idea of what I could be doing wrong or if I do have other food allergies appearing?

(Also, the doctors around here aren't any help. It was a pain to get my GI doctor to even test for Celiac, and when I got my endoscopy/colonoscopy, he focused on testing for Crohn's Disease.)

mommida Enthusiast

Well our experience with the elimination diet was due to eosinophils. (Your brief description of your doctor I am going to assume the lab work was not ordered for the pathology report.)

Advice on the elimination diet...

Eliminate all top 8 allergens and PEAS (if you suspect a food add it on your avoid list) 2 weeks

Introduce the challenge food in its purest form available, 3 days in a row, wait 2 weeks

Challenge each food one at a time, Journal everything i.e. amount of food, brands, reactions, BM, headaches, your environment, anxiety feelings and it might be helpful to see amount of sleep too.

Eosinophils are connected to food or airborn triggers. Once these white blood cells are activated, they are active for 12 DAYS with NO further stimulation.

I do not believe every one in the world has eosinophilic reactions going on :rolleyes: , but for the sake of going through a LONG, tedious, elimination diet ~ best to do it right the first time! ;)


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



Celiac.com Sponsor (A8-M):



  • 3 weeks later...
kayo Explorer

Similar experience for me too. You can see the details in my signature. It wasn't until my doc suspected fructose malabsorption and I went on the FODMAP diet did I truly start to feel better.

I say that this experience is like peeling an onion. Just when we think we have it figured out there's more layers to go.

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. - xxnonamexx replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      4

      My journey is it gluten or fiber?

    2. - cristiana replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

    3. - chrisinpa commented on Scott Adams's article in Skin Problems and Celiac Disease
      2

      Celiac Disease and Skin Disorders: Exploring a Genetic Connection

    4. - knitty kitty replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      4

      My journey is it gluten or fiber?

    5. - trents replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

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

    • Total Members
      132,698
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • xxnonamexx
      I read that as well but I saw the Certified Gluten free symbol that is the reason I ourchased it.
    • cristiana
      I agree, it so often overlooked! I live in the UK and I have often wondered why doctors are so reluctant to at least exclude it - my thoughts are perhaps the particular tests are expensive for the NHS, so therefore saved for people with 'obvious' symptoms.  I was diagnosed in 2013 and was told immediately that my parents, sibling and children should be checked.  My parents' GP to this day has not put forward my father for testing, and my mother was never tested in her lifetime, despite the fact that they both have some interesting symptoms/family history that reflect they might have coeliac disease (Dad - extreme bloating, and his Mum clearly had autoimmune issues, albeit undiagnosed as such; Mum - osteoporosis, anxiety).  I am now my father' legal guardian and suspecting my parents may have forgotten to ask their GP for a test (which is entirely possible!) I put it to his last GP that he ought to be tested.  He looked at Dad's blood results and purely because he was not anemic said he wasn't a coeliac.  Hopefully as the awareness of Coeliac Disease spreads among the general public, people will be able to advocate for themselves.  It is hard because in the UK the NHS is very stretched, but the fallout from not being diagnosed in a timely fashion will only cost the NHS more money. Interestingly, a complete aside, I met someone recently whose son was diagnosed (I think she said he was 8).  At a recent birthday party with 8 guests, 4 boys out of the 8 had received diagnosis of Coeliac Disease, which is an astounding statistic  As far as I know, though, they had all had obvious gastric symptoms leading to their NHS diagnosis.  In my own case I had  acute onset anxiety, hypnopompic hallucinations (vivid hallucinations upon waking),  odd liver function, anxiety, headaches, ulcers and low iron but it wasn't until the gastric symptoms hit me that a GP thought to do coeliac testing, and my numbers were through the roof.  As @trents says, by the grace of God I was diagnosed, and the diet has pretty much dealt with most of those symptoms.  I have much to be grateful for. Cristiana
    • knitty kitty
      @xxnonamexx, There's labeling on those Trubar gluten free high fiber protein bars that say: "Manufactured in a facility that also processes peanuts, milk, soy, fish, WHEAT, sesame, and other tree nuts." You may want to avoid products made in shared facilities.   If you are trying to add more fiber to your diet to ease constipation, considering eating more leafy green vegetables and cruciferous vegetables.  Not only are these high in fiber, they also are good sources of magnesium.  Many newly diagnosed are low in magnesium and B vitamins and suffer with constipation.  Thiamine Vitamin B1 and magnesium work together.  Thiamine in the form Benfotiamine has been shown to improve intestinal health.  Thiamine and magnesium are important to gastrointestinal health and function.  
    • trents
      Welcome to celiac.com @sha1091a! Your experience is a very common one. Celiac disease is one the most underdiagnosed and misdiagnosed medical conditions out there. The reasons are numerous. One key one is that its symptoms mimic so many other diseases. Another is ignorance on the part of the medical community with regard to the range of symptoms that celiac disease can produce. Clinicians often are only looking for classic GI symptoms and are unaware of the many other subsystems in the body that can be damaged before classic GI symptoms manifest, if ever they do. Many celiacs are of the "silent" variety and have few if any GI symptoms while all along, damage is being done to their bodies. In my case, the original symptoms were elevated liver enzymes which I endured for 13 years before I was diagnosed with celiac disease. By the grace of God my liver was not destroyed. It is common for the onset of the disease to happen 10 years before you ever get a diagnosis. Thankfully, that is slowly changing as there has developed more awareness on the part of both the medical community and the public in the past 20 years or so. Blessings!
    • knitty kitty
      @EndlessSummer, You said you had an allergy to trees.  People with Birch Allergy can react to green beans (in the legume family) and other vegetables, as well as some fruits.  Look into Oral Allergy Syndrome which can occur at a higher rate in Celiac Disease.   Switching to a low histamine diet for a while can give your body time to rid itself of the extra histamine the body makes with Celiac disease and histamine consumed in the diet.   Vitamin C and the eight B vitamins are needed to help the body clear histamine.   Have you been checked for nutritional deficiencies?
×
×
  • 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.