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

Have Been Told I Dont Have Coeliac


smile

Recommended Posts

smile Apprentice

I finally got some feedback regarding my raised IgA (blood tests results). My gp had spoken to a consulant I saw months back and they said I didn't have coeliac and they were pretty sure. They believed I either had IBS,a mild case of malabsorption. It was suggested I take something called Colestyramine. I then told them that since being gluten free Ive had normal bowel movements. No problem on that front. So dont have to take that. A last resort is to try a lactose free diet. Now I dont believe I have IBS. My bowel movements are normal eg formed and once a day. I dont have stomach cramps nor have I ever been constipated. I explained that Im still having weight loss and feeling sick. I was told if it continues to go back and see them again. My parents were like "how much weight do you need to lose to get help". Im almost down to 6st 11. Some of my size 8 (uk) clothes are falling off me, if I were to not wear jumpers/hooded tops, people would actually think I dont eat properly. Sometimes I feel paranoid that people think I have an eating disorder. Does anyone know of anything that could be going on. I spoke with my GP about previous history of overdoses on medication and asked if they could contribute to my health now and they said they were pretty sure it wouldnt have caused any damage. I was also told I can eat whatever I want eg gluten containing foods.


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



Celiac.com Sponsor (A8-M):



mushroom Proficient

Sometimes you have to get off the medical motorway and take a byway :rolleyes: The motorway keeps you travelling on a known path with no deviations which leads to a known destination; the byway allows you to explore other small towns along the way and consider the opportunity of visiting other places.

It is MHO that you need to stop eating gluten regardless of the tests and the good doctors' opinions. It is your body and you are in control of it. The testing is just not sufficiently accurate to abide by it 100%. Even in cases of quite severe damage to the small intestine it is possible to have an equivocal or "normal" blood result. Even in cases of celiac disease with other than GI symptoms it is possible to have a "normal" endoscopy with biopsy. The false negative rate is about 20%. The ultimate test of whether or not gluten is a problem for you is to stop eating it. I know you have had gluten free trials before. I believe that if you were to give it a good, three-month trial where you were totally strict in eliminating all sources of gluten - and there are oodles of threads on here on how to do this - that you would feel much better and stop losing the weight. You should of course also eliminate lactose because you have not had an endoscopy and we do not know if you have damaged villi, but let's assume you do and that you are not making much lactase. You would also need to find a way to convince your doctor to check you for vitamin and mineral deficiencies and supplement these in your diet. If you have any of the standard deficiencies Vits. D, B12, folic acid, A, E, K, and minerals potassium, magnesium, calcium, zinc, these could all have severe impacts on your health. You will probably need to have your thyroid tested too to be sure. If after all this you continue to lose weight then your doctors should do a thorough investigation as to why.

Now this is just my opinion, but to me you look like a classic (semi-)silent celiac. The fact that you don't have raging GI or neurological issues means nothing. My sister's major symptom was unexplained weight loss.

Good luck to you on your byway travels. :)

WheatChef Apprentice

You can safely ignore the advice of any doctor who uses the term "IBS" without immediately following it up with "doesn't exist". If going gluten-free has produced a significant decrease in severity of symptoms then who cares what faulty tests show?

Kay DH Apprentice

It would be good for you to keep a food diary, both to track any reactions that you might have and to see if you are getting enough calories. Your doctor should have run a poop test to determine if there are any pathogens in your GI tract that are influencing absorption, and to check malabsorption. Make sure you are not getting cc'd from all the places that gluten hides, such as in most prepared foods. "IBS" is a name that doctor's assign to GI problems that are not diagnosed. We have a friend that has had IBS for years, and he just went gluten-free for other health reasons. His IBS disappeared. The final test is how you feel gluten-free. Even if you don't have celiac, you could have sub-clinical celiac or gluten sensitivity. There is also the possibility of other food sensitivities.

cassP Contributor

i dont know STONES... and is a size 8 in the UK the same as in the US?? are you sickly thin?? it might be possible that you are dropping weight now because you're off the gluten..??? the weight comes off of me when i go gluten free- and if i am doing LOW to NO carb- it comes off even faster..

idk, as long as you're still healthy & have enough fat percentage to keep your organs healthy- and as long as your bowels are normalizing- i wouldnt worry .. but keep up with the doctor of course with any concerns.

mushroom Proficient

A stone weighs 14lbs (well, not every stone, of course :P but the ones on the scale). So she weighs 95 lbs.

smile Apprentice

Thanks for your replies. I guess my main concerns are the feeling sick and losing weight. Ive decided that Im going stay gluten free, my dietician had told me whether Im diagnosed or not I should stay well away from gluten. Another thing that has seemed to have disappeared slowly over the last three weeks is a rash I would get on my legs. It just would always be there, however it has totally been gone for at least a week now and my legs dont itch as much. I am also going to go lactose free, from what I remember when I have eaten things like cheese pizza or jacket potatoes with cheese I tend to not feel great afterwards. Funnily enough I had a gluten free cheese pizza on saturday, both sunday and monday I felt sick, had slight headache etc. Im shocked that even the specialist (saying that I never actually met them because they were always off sick) hasnt even considered that I could be coeliac or have non coeliac gluten intolerance, plus no mention has been made by them about my rasied IgA. It seems that it has no importance. I will just have to follow eating what makes me feel better and not hang around for a specialist to confirm what I am doing is right.


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



Celiac.com Sponsor (A8-M):



cassP Contributor

plus no mention has been made by them about my rasied IgA. It seems that it has no importance. I will just have to follow eating what makes me feel better and not hang around for a specialist to confirm what I am doing is right.

what raised Iga?? is it your Total Iga Serum??? or is it Tissue Transglutamase Iga? or Antigliadin Iga??

we could probably explain more to you- the doctors seem to only give us a millisecond of their time...

and you're a size 8??? but only @ 95lbs????? im worried about you- 95 is too thin.. i hope you can heal soon and get to a weight that is healthy & makes u happy :) try to eat some rice with every meal... and make sure you're getting enough healthy fats, proteins, & veggies..

keep us posted- and share your Iga item- im interested...

smile Apprentice

Thanks for your reply. The doctors have never been concerned with the weight to be honest. I was told by a registerar that I have always been light when he has only seen me twice and a few year back I was 36lbs heavier and when I was at college I was averaging around 122lbs, for me that is my normal healthy weight.

Im going to see if my diet changes make anymore difference in say a month. In my daily diet I get fruit/veg/yoghurt/nuts/gluten free bread/meats/poatoes or rice and chocolate soya milk.

I was never told what IgA it was. All I was told was that my blood test showed normal for one idicator of coeliac, but the other one was slightly raised (the IgA). I was told that this suggest I should see a specialist. However my doctor spoke to the specialist and they said I definately didnt have coeliac. I wont be seeing my doctor for a while for any reason so wouldnt be able to find out what IgA it was. They are not very fourth coming in giving details. This raised IgA has been the same for the past year, Im assuming that means Im producing antibodies for some reason.

Ive also noticed that since being gluten free that Im losing less hair. Usually when I wash it you could pick up a clump of it, now there is about 3 hairs, which is pretty normal. Im glad to be seeing some changes.

Im just a bit worried because coming up shortly I have to go somewhere (they are providing lunch)and I know that if I dont eat anything people are going to assume I have an eating problem (even more so with how thin I look), mental health. It would be easier to say I have coeliac than to say I choose not to it gluten. Im afraid of being judge as choosing to not eat certain foods. I know what some of the people Im going to be around are like and they are professionals. Any idea how I can deal with the situation. Im not going to eat there anyway, Im going to eat before going. I just dont want to be judged and looked at as if I have a problem when I dont.

ravenwoodglass Mentor

Ive also noticed that since being gluten free that Im losing less hair. Usually when I wash it you could pick up a clump of it, now there is about 3 hairs, which is pretty normal. Im glad to be seeing some changes.

Im just a bit worried because coming up shortly I have to go somewhere (they are providing lunch)and I know that if I dont eat anything people are going to assume I have an eating problem (even more so with how thin I look), mental health. It would be easier to say I have coeliac than to say I choose not to it gluten. Im afraid of being judge as choosing to not eat certain foods. I know what some of the people Im going to be around are like and they are professionals. Any idea how I can deal with the situation. Im not going to eat there anyway, Im going to eat before going. I just dont want to be judged and looked at as if I have a problem when I dont.

It sounds like the diet is helping you. Good to hear. About that lunch, the people are not going to have access to your medical records. If it is easier to just say you are celiac then do so. Or you could just say you have food allergies and then change the subject. Try not to worry about what others think your health is more important.

Jestgar Rising Star

and you're a size 8??? but only @ 95lbs?????

An 8 UK is a 6 US Open Original Shared Link

smile Apprentice

sorry to be writing another post.

Im just so fed up. For a good number of years Ive not been well eg depression. Now Ive turned things around, but physically Im falling apart. I just dont know what to do anymore.

Ive been gluten free almost 4 weeks now and Ive been lactose free for about 4-5 days. Now this last 3/4 days Ive been having slight headaches. Then today I had a heavy head again, it went away after about 15 mins, however I then had about 4 trips to the bathroom for bowel movements. I also had lost of noises from my stomach and wind. I cant think of anything that Ive eaten that can have caused this.

Then about an hour later I noticed that one of my fingers was swollen, there is no redness or itching. I dont think Ive been biten by anything.

Ive seen so many gps about feeling physically unwell in the last year. I just want to be physically well now to make everything more complete.

Marz Enthusiast

You mentioned gluten-free bread and soya - you might want to leave those out for a few days and see if it makes a difference. Many gluten-intolerants/celiacs are also intolerant to soya. Gluten-free bread may have trace amounts of gluten cc, or you may be intolerant to some grains while you're still healing. It's always a good idea to keep a food diary with your symptoms and see if you can spot any patterns.

Also, 4 weeks is a short amount of time - I've been gluten free for a few months and I'm still struggling to figure out what is safe for me to eat, accidentally glutening myself etc. Every time I accidentally eat a trace amount of gluten, all the symptoms start up again. Although overall I can see I'm much better than when I started.

Might be worth it to think back to how ill you were before you started gluten free - if you can see improvement then you're on the right direction, you just need to be patient with your body's healing. If you can't see improvement then either you're still getting some trace cc or you're intolerant to some other food as well? For example, egg, chicken, olives, goat cheese - all these items give me severe d a day or so later. I would never have picked this up without a food diary, and avoiding them helps me immensely.

Hope you feel better soon!

reddgreen Newbie

I just found this blog today, and also just found coeliac/gluten allergy symptoms described almost exactly what Ive been dealing with for years, hoping to get tested in the next couple of weeks.

Many of these tests have a very high false negative rate, so a doctor might not interpret a negative result correctly. Try to find a site, or ask your doctor (or get a new doctor!!!) what the false negative rate is for the test as well as the accuracy of the test (the probability that the test does signal positive if the disease is present). I have a background in math and statistics, so ive seen the math behind some medical tests.

Best luck to you, and I agree with the advice above: just because the test was negative doesn't mean you aren't coeliac or gluten intolerant. If eliminating gluten from your diet gets rid of the symptoms, then power to you!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,398
    • Most Online (within 30 mins)
      7,748

    Megannnnn
    Newest Member
    Megannnnn
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Scott Adams
    • Scott Adams
      I had the same thing happen to me at around your age, and to this day it's the most painful experience I've ever had. For me it was the right side of my head, above my ear, running from my nerves in my neck. For years before my outbreak I felt a tingling sensation shooting along the exact nerves that ended up exactly where the shingles blisters appeared. I highly recommend the two shot shingles vaccine as soon as your turn 50--I did this because I started to get the same tingling sensations in the same area, and after the vaccines I've never felt that again.  As you likely know, shingles is caused by chicken pox, which was once though of as one of those harmless childhood viruses that everyone should catch in the wild--little did they know that it can stay in your nervous system for your entire life, and cause major issues as you age.
    • trents
    • Clear2me
      Thanks for the info. I recently moved to CA from Wyoming and in that western region the Costco and Sam's /Walmart Brands have many nuts and more products that are labeled gluten free. I was told it's because those products are packaged and processed  in different  plants. Some plants can be labeled  gluten free because the plant does not also package gluten products and they know that for example the trucks, containers equipment are not used to handle wheat, barely or Rye. The Walmart butter in the western region says gluten free but not here. Most of The Kirkland and Members Mark brands in CA say they are from Vietnam. That's not the case in Wyoming and Colorado. I've spoken to customer service at the stores here in California. They were not helpful. I check labels every time I go to the store. The stores where I am are a Sh*tshow. The Magalopoly grocery chain Vons/Safeway/Albertsons, etc. are the same. Fishers and Planters brands no longer say gluten free. It could be regional. There are nuts with sugar coatings and fruit and nut mixes at the big chains that are labeled gluten free but I don't want the fruit or sugar.  It's so difficult I am considering moving again. I thought it would be easier to find safe food in a more populated area. It's actually worse.  I was undiagnosed for most of my life but not because I didn't try to figure it out. So I have had all the complications possible. I don't have any spare organs left.  No a little gluten will hurt you. The autoimmune process continues to destroy your organs though you may not feel it. If you are getting a little all the time and as much as we try we probably all are and so the damage is happening. Now the FDA has pretty much abandoned celiacs. There are no requirements for labeling for common allergens on medications. All the generic drugs made outside the US are not regulated for common allergens and the FDA is taking the last gluten free porcine Thyroid med, NP Thyroid, off the market in 2026. I was being glutened by a generic levothyroxin. The insurance wouldn't pay for the gluten free brand any longer because the FDA took them all off their approved formulary. So now I am paying $147 out of pocket for NP Thyroid but shortly I will have no safe choice. Other people with allergies should be aware that these foreign generic pharmaceutical producers are using ground shellfish shell as pill coatings and anti-desicants. The FDA knows this but  now just waits for consumers to complain or die. The take over of Wholefoods by Amazon destroyed a very reliable source of good high quality food for people with allergies and for people who wanted good reliably organic food. Bezos thought  he could make a fortune off people who were paying alot for organic and allergen free food by substituting cheap brands from Thailand. He didn't understand who the customers were who were willing to pay more for that food and why. I went from spending hundreds to nothing because Bezo removed every single trusted brand that I was buying. Now they are closing Whole foods stores across the country. In CA, Mill Valley store (closed July 2025) and the National Blvd. store in West Los Angeles (closed October 2025). The Cupertino store will close.  In recent years I have learned to be careful and trust no one. I have been deleberately glutened in a restaurant that was my favorite (a new employee). The Chef owner was not in the kitchen that night. I've had  a metal scouring pad cut up over my food.The chain offered gluten free dishes but it only takes one crazy who thinks you're a problem as a food fadist. Good thing I always look. Good thing they didn't do that to food going to a child with a busy mom.  I give big tips and apologize for having to ask in restaurants but mental illness seem to be rampant. I've learn the hard way.          I don't buy any processed food that doesn't say gluten free.  I am a life long Catholic. I worked for the Church while at college. I don't go to Church anymore because the men at the top decided Jesus is gluten. The special hosts are gluten less not gluten free. No I can't drink wine after people with gluten in their mouth and a variety of deadly germs. I have been abandoned and excluded by my Church/Family.  Having nearly died several times, safe food is paramount. If your immune system collapses as mine did, you get sepsis. It can kill you very quickly. I spent 5 days unconscious and had to have my appendix and gall bladder removed because they were necrotic. I was 25. They didn't figure out I had celiac till I was 53. No one will take the time to tell you what can happen when your immune system gets overwhelmed from its constant fighting the gluten and just stops. It is miserable that our food is processed so carelessly. Our food in many aspects is not safe. And the merging of all the grocery chains has made it far worse. Its a disaster. Krogers also recently purchased Vitacost where I was getting the products I could no longer get at Whole Foods. Kroger is eliminating those products from Vitacost just a Bezos did from WF. I am looking for reliable and certified sources for nuts. I have lived the worst consequences of the disease and being exposed unknowingly and maliciously. Once I was diagnosed I learned way more than anyone should have to about the food industry.  I don't do gray areas. And now I dont eat out except very rarely.  I have not eaten fast food for 30 years before the celiac diagnosis. Gluten aside..... It's not food and it's not safe.  No one has got our backs. Sharing safe food sources is one thing we can do to try to be safe.        
    • Mmoc
      Thank you kindly for your response. I have since gotten the other type of bloods done and am awaiting results. 
×
×
  • 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.