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

Glutened Or New Allergy?


annegirl

Recommended Posts

annegirl Explorer

I've been gluten free since the end of January and I've seen a HUGE change for the good in all my crazy symptoms.

My problem now is that the D that I had intermittently is now coming on worse and I have a lot of rumbling in my stomach after consuming different foods. It's getting hard for me to tell which food I'm reacting to. I don't know if I'm continuing to react to say, what I had for breakfast because I will have worse D at night so maybe it could be dinner too???

Today for example: I had applesauce (I made it myself from homegrown apples) and corn chex for breakfast. I started feeling sick a bit after, broke out in some hives and all over felt sick, so I figured the chex were on my no list for now....but fastforward to dinner and all of a sudden my stomach is rumbling worse and I have bad D. I don't know if that's a continued reaction from the chex or if I've added a new issue to my list of things I can't eat (gluten, soy, rice, lactose). I make all my food myself, I'm eating basically fruits, veggies, potatoes and chicken or hamburger. The chex was the only thing I was eating packaged and listed "gluten free." For dinner I made a soup with black beans, hamburger, tomato sauce and green chilies and a salad with olive oil dressing.

Can something that you're reacting to last all day and display worse symptoms 12 hours later? I'm just feeling like I'm going a little crazy. I'm still feeling great in between discovering things that make me sick, and I'm more than willing to cut stuff out while I'm hyper sensitive and add them in slowly later....I just need to know what it is I'm reacting to!

Any ideas? Thanks in advance!


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

What are you putting on the Rice Chex as a milk alternative?

Yes the reaction to something you are intolerant to can show up later in the day or even a few days later. It can make it hard to pinpoint what it is that is getting us. A symptom and food log can be helpful in finding a pattern.

Tigercat17 Enthusiast

I'm really sensitive and I know I can't eat any of the Chex cereals. I tried them all & I always get acid reflux, a sore throat and a tender tummy the next day. It usually lasts for three days. This is my usual gluten reaction, but I'm not sure if there's CC of gluten in the Chex or not or if I'm reacting to something else in them. It's still a mystery to me. :unsure: It sounds like your reacting to them also. I just wouldn't eat them & see if you feel better. If you haven't started a food journal already, it would be a good idea to start one & see if you react to other foods. It really helps me since I always get reactions the next day.

I hope you feel better! :)

jenngolightly Contributor

Today for example: I had applesauce (I made it myself from homegrown apples) and corn chex for breakfast. I started feeling sick a bit after, broke out in some hives and all over felt sick, so I figured the chex were on my no list for now...

Hives is an allergic reaction that will show up right after eating a food you are allergic to. Do you know if you are allergic to a certain food?

Intolerance side effects can show up long after you eat the food, so your D might be a reaction to food you ate yesterday.

Do you keep a food diary? That will help you pin point which foods are giving you problems. If you find that you get hives every time you eat corn chex, you might be allergic to something in the chex. Or, if you get D every time you eat your home made applesauce, then something in it is giving you D.

annegirl Explorer

Ok, so starting a food journal right away. I've been meaning to for a couple weeks but I'm doing it for real now.

Yes, the chex are way gone. I'm giving them to my sister to eat.

I will just start writing everything down when I get symptoms and after a while I'm sure patterns will pop out.

Interestingly enough, I am having more gastric issues now that I'm gluten free than I did before....it's like I'm finally giving my system enough of a break to try and deal with stuff and it's extra sensitive. My other symptoms are so incredibly improved I can't believe it. I've gone from needing 9-10 hours of sleep (and still feeling tired) to now not being tired enough to sleep until after 12 and getting up 6 hours later ready to greet the day! I feel like a new person, so I can deal with a little cramping and D while everything shakes out.

Thanks again!

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
      132,694
    • Most Online (within 30 mins)
      7,748

    Aanhmcbride
    Newest Member
    Aanhmcbride
    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.