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

Really Confused


Spike23

Recommended Posts

Spike23 Newbie

Hi everyone,

Would really appreciate some insight.

For the past three years i have had gas, runs, tiredness etc. I had just come back from a stint o/s so doctors sent me for numerous tests to see if i had contracted some sort of o/s parasite-no!

THEN i was diagnised with IBS, i had heard about gluten intolerances and went to my doctor to get a blood test and since then have had three more..all came back negative.

When i went to see a specialist he was like again you have IBS but i will do a gastroscopy/colonoscopy to apease you but i am sure you have IBS. I became frusrated and never had the tests done and thought well maybe i do have IBS as life is stressfull.

I then went to a Naturopath who informed me i am Gluten Intolerant and Lactose Intolerant! When i heard this i was annoyed thinking what on earth am i meant to eat now and no more chocolate!

Anyway, i went on this new diet and after a week began to feel a bit better but i relapsed and had some chocolate biscuits the other day and within half an hour i was sick but i was sicker than i ever have been before, is this because my body was beginning to get used to having No gluten and lactose?? AND my body responded so bad because of the reaction...How long does it take for Glutent to leave your body..???

This whole thing can be so annoying and if i do eat such food i am literally sick for a few days?? Does this happen to others?? I Am really confused!!!

Again would apprecaite any insight??

Thanks ;)


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



Celiac.com Sponsor (A8-M):



gfmolly Contributor

Your story sounds very much like mine. It does take awhile for your body to heal. I am on month 4 and when I get glutened, it takes about a week for my bm's to be normal and for me to feel energized. You may have celiac, the biopsy is the gold standard of diagnosis. If you respond to the gluten free diet, then you probably need to be gluten free, especially since you reacted so strongly to your mistake. If you do want a diagnosis with a biopsy, then you need to continue to eat gluten until you have it done. Unfortunately, you may get another false negative if you don't. It sounds like the naturpath can help guide you through this experience. This forum is great for getting answers! Good luck and welcome.

A couple things that might help you as you heal:

you may want to try a probiotic to help get some good bacteria in your system

alot of people have great lists for first timers on their personal accounts. Noglugirl has a really good list that can help get you started.

Terri

par18 Apprentice

Just give the diet a chance. Concentrate on doing what is necessary to feel better and see what happens. A negative response to a relapse is an indication in itself. Take it one step at a time. Understand that if you have to give up something (gluten) you have the possibility of getting something (a better quality of life) in return. Think positive and good luck.

Tom

Guest j_mommy

Yes, When I get glutened or CC'd I am not myself for days!!! big D and EXHAUSTED!!!!

Hang in there...the first few weeks are hard but it gets easier.

Also you said you were going to do an endoscopy...if you are interested in checking for celiac you need to be eating gluten!!!!

ravenwoodglass Mentor
Hi everyone,

Would really appreciate some insight.

For the past three years i have had gas, runs, tiredness etc. I had just come back from a stint o/s so doctors sent me for numerous tests to see if i had contracted some sort of o/s parasite-no!

THEN i was diagnised with IBS, i had heard about gluten intolerances and went to my doctor to get a blood test and since then have had three more..all came back negative.

When i went to see a specialist he was like again you have IBS but i will do a gastroscopy/colonoscopy to apease you but i am sure you have IBS. I became frusrated and never had the tests done and thought well maybe i do have IBS as life is stressfull.

I then went to a Naturopath who informed me i am Gluten Intolerant and Lactose Intolerant! When i heard this i was annoyed thinking what on earth am i meant to eat now and no more chocolate!

Anyway, i went on this new diet and after a week began to feel a bit better but i relapsed and had some chocolate biscuits the other day and within half an hour i was sick but i was sicker than i ever have been before, is this because my body was beginning to get used to having No gluten and lactose?? AND my body responded so bad because of the reaction...How long does it take for Glutent to leave your body..???

This whole thing can be so annoying and if i do eat such food i am literally sick for a few days?? Does this happen to others?? I Am really confused!!!

Again would apprecaite any insight??

Thanks ;)

You just did a gluten challenge. The results were positive. It is common for the symptoms to become worse after going gluten free and then getting poisoned. Your body is going to tell you in no uncertain terms that if does not want you eating it again. This is how some of us who are unfortunate and have false negatives on blood work are diagnosed. Unfortunately in my case it took 15 years for a doctor to think to suggest it. It took 2 weeks off gluten and then 3 days on for my body to react violently. That was 5 years ago, after 40 years of debilitating neuro and joint problems and 15 years of serious illness and thousands of dollars for tests.

hathor Contributor

You've gotten some good advice.

All I can add is -- dark chocolate, hon! Come over to the good stuff -- you won't want your chocolate adulterated with dairy ever again :lol: In addition to the straight stuff, I've seen recipes & mixes for chocolatey delights that are also dairy free. Despair not :wub:

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

      Issues before diagnosis

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

      Celiac Disease and Skin Disorders: Exploring a Genetic Connection

    3. - knitty kitty replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      My journey is it gluten or fiber?

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

      Issues before diagnosis

    5. - trents commented on Jefferson Adams's article in Other Diseases and Disorders Associated with Celiac Disease
      6

      Celiac Disease Patients Face Higher Risk of Systemic Lupus

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

    • Total Members
      132,692
    • Most Online (within 30 mins)
      7,748

    Ali Zaib
    Newest Member
    Ali Zaib
    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

    • 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?
    • sha1091a
      I found out the age of 68 that I am a celiac. When I was 16, I had my gallbladder removed when I was 24 I was put on a medication because I was told I had fibromyalgia.   going to Doctor’s over many years, not one of them thought to check me out for celiac disease. I am aware that it only started being tested by bloodwork I believe in the late 90s, but still I’m kind of confused why my gallbladder my joint pain flatulent that I complained of constantly was totally ignored. Is it not something that is taught to our medical system? It wasn’t a Doctor Who asked for the test to be done. I asked for it because of something I had read and my test came back positive. My number was quite high.Are there other people out here that had this kind of problems and they were ignored? 
×
×
  • 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.