Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Negative Biopsy


LolaK

Recommended Posts

LolaK Newbie

Hi I'm new on here.

My 16 year old son has been ill for the last 2 years, mostly exhaustion and low immune system plus leg and back pains - loads of time off school and recently sore abdomen, bloating and gas. He had Glandular Fever 2 year sago and the GP thought it was post viral syndrome but tested him for coeliac and the blood test was positive. 1 month later he had the biopsy. In that month running up to it he was getting sicker and sicker, coming home from school and going straight to bed.

So the day of the biopsy, as soon as he was ready to eat we started a Gluten free diet. The change was immediate. Not just physical such as gaining some weight more energy but also he became a joy to be with again. He had been so moody and aggressive for the past few years he was so hard to live with.

And now as the title suggests we just received the result of a negative biopsy! I am really shocked as he responded so well and also had no time off school since being on the gluten-free diet (he's in the middles of important exams)

Being 16 I know he will not want to stick to the diet very carefully now he thinks he has got Coeliac disease. I feel so disillusioned with it all - I just want him to be well.

Any ideas what next? (He has an appointment next week with consultant at Barts Hospital).


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



Celiac.com Sponsor (A8-M):



zus888 Contributor

Did the transgultaminase tests come back positive? Just because they didn't find it doesn't mean it's not there. Plus, celiac is just one "symptom" of gluten intolerance. Celiac is just gluten intolerance with villous blunting or atrophy. If he has gluten intolerance, he still will have ALL the same risks in terms of his general health and well-being. If he tested positive for the antibody test, then his body has developed them because it thinks that gluten is not food and is attacking it. This causes a number of problems including chronic inflammation which leads to a whole host of other problems. My suggestion is to keep him on the gluten-free diet, and to do what you can to get him diagnosed with gluten-intolerance or celiac. Remember celiac is just ONE FORM of gluten intolerance, you could even consider it a symptom of it. And, as you know, not everyone gets the same symptoms. Ask questions regarding his diagnosis and the chances of the biopsy missing something. Ask questions about his blood test results (like, why would he have antibodies to gliadin or transglutaminase). Ask if they will diagnose him based on the diet (and maybe a challenge). If they won't, you should find another doc who is more familiar with celiac/gulten intolerance. The only reason why I suggest trying to get the diagnosis is because he is in school. The school will be required BY LAW to offer gluten-free lunches (if they don't already do that) if he needs it for his health. But I'm fairly sure that they will require a diagnosis before they go spending extra time and money to do it.

Good luck.

I'd also like to add that if you can get him completely gluten free (check his medications too), he might be willing to stick to the diet because of how good he feels and feeling the consequences of being glutened.

zus888 Contributor

I also want to say that I'm fairly new to this, so the others might have more to say. I am reading a book called "Healthier Without Wheat" and it has been extremely enlightening, and pretty much where I'm getting all my information from. I strongly suggest you read it.

etta694 Explorer

I have been fighting different symptoms for many years, doctors finding tests 'normal' for whatever they tested for. I finally found info online that pointed me towards gluten. I was scheduled for a colonoscopy, endoscopy, and biopsy (I asked about Celiac disorder). The results? Everything was wonderful, my intestines showed no disease whatsoever. Since cutting out gluten - any form of it, I have my life back. I feel great, I am not exhausted, I have great digestion, I am not bloated, sick, I don't have a chronic cough,etc. Test results don't always indicate the whole story.

LolaK Newbie

zus888 and etta694, Thank you both for your responses. Both very helpful and informative.

I've been reading a few posts on here about diagnosis and it seems they should be taking tissue from multiple sites? Well it seems like they only took 3 samples from my son. Also He had one positive blood test and that was followed by a negative one that the consultant did. They noticed on the endoscopy that he had small patches of duodenitis - not sure of significance of that.

Well we are going to continue gluten free although my sons initial reaction to the negative biopsy was celebration I know he realises the effect that Gluten has on him. and we will see what the consultant says Thursday.

What is interesting is that he has always craved bread and similar products and even when he was a toddler he would over eat on bread and it always followed by screaming and colic.

I will update on Thurs.

Lola

ravenwoodglass Mentor

The change was immediate. Not just physical such as gaining some weight more energy but also he became a joy to be with again. He had been so moody and aggressive for the past few years he was so hard to live with.

You are doing the right thing by keeping him gluten free. For some of us brain impact can occur before the gut damage becomes severe. Also damage can be patchy and if the right area is not biopsied you can end up with a false negative. The combination of positive blood work followed by the positive changes on the gluten-free diet is significant in showing the diet is what he needs.

LolaK Newbie

You are doing the right thing by keeping him gluten free. For some of us brain impact can occur before the gut damage becomes severe. Also damage can be patchy and if the right area is not biopsied you can end up with a false negative. The combination of positive blood work followed by the positive changes on the gluten-free diet is significant in showing the diet is what he needs.

Thank you Ravenwood, we will be doing our best to keep him gluten free, I will be interested to hear what consultant says on Thursday.

Does anyone know if the Duodenitis is significant? Is it normal for someone so young to have this?

Thanks Lola


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



Celiac.com Sponsor (A8-M):



eatmeat4good Enthusiast

Lola,

My son is 16 also.

We didn't do testing, but he had been sleeping every moment not in school, had severe asthma and a stumbling gait and leg pain. Irritability and moodiness and depression.

It all cleared up in a few days gluten free and returned on gluten challenge.

I tried to get him to try gluten free a few weeks after I did. He gave me 4 days and I noticed a big difference. Then he ate pizza with friends. He was sick for 4 days and I mean bad. All the symptoms hit hard. I was kind of thankful for that because after that episode he is completely vigilant about gluten avoidance. He feels better without it.

Maybe your son is relieved that the bad symptoms went away when he didn't eat gluten.

Even without testing postive, he may decide to stay gluten free on his own. Especially if he has a reaction when he tries eating gluten again. You may have to have a few "episodes", but usually if gluten is a problem, the sensitivity increases.

That means you CAN'T got back to eating gluten even if you want to.

I hope your tests are definitive, but if they are not, I hope your son chooses gluten free for himself if he feels better that way. No one likes feeling tired and moody and depressed. So even if he goes back to gluten for a time, you can always help him by letting him know about his symptoms and reminding him how well he felt off of gluten. Gluten intolerance is just as serious as Celiac for the damage to the quality of life to the individual.

Does he notice how much better he feels and behaves off of gluten? Maybe that will be enough to keep him gluten free. I don't know about the duodenitis...but it certainly sounds suspicious of Celiac disease doesn't it?

I gave my son articles on Gluten Intolerance and Celiac. They helped him understand his symptoms and it was a relief to him to find out he can live normally now.

LolaK Newbie

Thanks Eatmeat4good for sharing that with me, sounds like a similar picture in many ways. We live in the UK so with a positive biopsy you can get gluten free foods on prescription, which I was hoping for, but that's maybe not to be.

I was surprised at how well he has accepted the diet, but he did have a burger after the first week "just to see" and he felt rotten for about 3 hours afterwards with stomach pains and gas. He was in a terrible mood and picked a fight with his younger sister and everything dissolved into chaos and I realise that we have gone through so many scenes like this that could have been avoided had we known..

The next day he was feeling mostly better but tired and we talked about the effect it had had on him.

I will update after Thursday when he see the consultant but we are staying gluten-free.

ravenwoodglass Mentor

Thank you Ravenwood, we will be doing our best to keep him gluten free, I will be interested to hear what consultant says on Thursday.

Does anyone know if the Duodenitis is significant? Is it normal for someone so young to have this?

Thanks Lola

Duodenitis means the duodenum is showing some inflammation. That is not unusual with celiac. From reading your last post it is good that he is seeing good results on the diet and his reaction to adding in that bit of gluten may help him realize how harmful it is to his body. I hope he is feeling better soon.

LolaK Newbie

Just thought I would update as we went to hospital for follow up. I thought it would be frustrating, but it was worse than that.

The registrar was different to last time. she started by saying "good news the biopsy was negative and so was the blood test" (they did a second test at the first appointment). she asked J how he was and he said that he had gone gluten-free as soon as he had biopsy done, that he was feeling better now, more energy, hadn't missed school and was putting on weight. He also said that when he had eaten bread or pastry had felt terrible in his stomach and aching had returned.

She looked incredulous and said that was great but he didn't have coeliac disease and they can't give him a diagnosis.

So I asked her why she thought he had improved and she said because some people don't react well to wheat or gluten. She said she would go and ask consultant if J could stay on the diet and maybe do a challenge at a later point. She came back and said "Dr L says he definitional does not have coeliac and that he should be discharged from his care. he can continue with diet if he wished but he isn't coeliac"

I told her that the last registrar had said that if the biopsy was negative they would look for other reasons why he was so ill. But she said because he is better there is no need and they don't do that anyway.

I have never come across such an illogical argument.

I realise that staying on the diet is the answer, but she was telling my son he doesn't have it and that seed is planted firmly in his mind now. It was a complete waste of time and I feel so mad!

ravenwoodglass Mentor

It can be really frustrating. The good thing is that he has seen the improvement on the diet and he has felt awful when he ate gluten after being on it. Hopefully he will stick with the diet and his reactions will be enough to keep him compliant.

eatmeat4good Enthusiast

I'm so sorry that medical appointment was worthless.

Your son had a similar reaction to my son in mood disruption and behavior problems and stomach aches. I wouldn't have been able to keep him on it without the reactions. But each and every time there has been a mistake or challenge he gets really sick.

Sorry you didn't get help with gluten free foods, but I hope your son's improved health, mood and behavior continue. It is really a joy several months down the road to watch my son thriving. I hope it happens to your son too.

While my son was intitially reluctant to try the diet, it worked. He initially didn't want to talk about it with any teachers or peers either. But he has grown with it and he now tells certain peers at school about the effects of gluten. One peer he noticed appeared to be very drowsy and mentally absent in class. He said, "Mom, I remember when I felt like that every day so I just had to tell him about it." It is amazing what can come from being gluten free. It is kind of a process of accepting it, then sharing it. I think your son may get there too.

I hope your son will come to understand that Gluten Intolerance is just as serious as Celiac and I hope he will stay on the diet.

Wishing you well.

mushroom Proficient

Unfortunately, there are too many doctors who do not believe there is such a thing as non-celiac gluten intolerance. They have not been taught it and therefore it doesn't exist. Doctors are like that. They can look the obvious in the eye, and because it is not in their experience or data base they will tell you flat out that black is white. If you are not celiac, gluten is not a problem :wacko:

Sorry doc(s) but for ever so many of us it is, and we don't need you to tell us. Our bodies tell us the answer and I don't give a darn what you learned in medical school 20 years ago before they even became aware that people who are not celiac can have gluten problems. Read the literature, go to the continuing education seminars, get up to date.

The reason so many people are suffering is because of the medical profession's obsession with the celiac diagnosis. Celiac is just the form of gluten intolerance they have developed a test for, in my book. Now those of a scientific bent will argue otherwise, because science rules over experience, but I say, why listen to science when it is going to ruin your health. Do what makes your body feel better. :)

zus888 Contributor

Sorry to hijack the thread, but does a positive gliadin antibody result point to gluten intolerance? Seems to me that anyone with a positive gliadin result would be considered gluten intolerant. And I'm willing to bet that there are a lot more false negatives (translating to more undiagnosed ppl) on that test as well.

ravenwoodglass Mentor

Sorry to hijack the thread, but does a positive gliadin antibody result point to gluten intolerance? Seems to me that anyone with a positive gliadin result would be considered gluten intolerant. And I'm willing to bet that there are a lot more false negatives (translating to more undiagnosed ppl) on that test as well.

If you are making antibodies to gluten you are celiac or 'gluten intolerant'. Either way the person should avoid gluten strictly.

LolaK Newbie

If you are making antibodies to gluten you are celiac or 'gluten intolerant'. Either way the person should avoid gluten strictly.

What about a positive blood test followed by a negative one? Is this common?

Thanks for all the positive comments by the way, I was feeling pretty disillusioned!

Lolax

zus888 Contributor

Ravenwoodglass, I was under the impression that celiac disease was a gluten intolerance that also causes the body to attack the duodenal villi - that basically it's just one outcome of gluten intolerance.

Positive transglutaminase antibody indicates that antibodies are directed against the enzyme in the intestines called tissue transglutaminase (tTG), which would be one of the indicators of celiac.

However, a positive gliadin antibody only shows that the body is attacking the gliadin in gluten (as opposed to giving an indication of the body attacking itself). I'm just thinking that a positive gliadin antibody should be indicative of gluten intolerance, at the very least.

I believe both to be serious diseases since they both involve the immune system and will create chronic inflammation within the body, which we all know causes a multitude of other health problems. And either way, both require the strict adherence to a gluten-free diet.

LolaK Newbie

Well, my son is well and truly on gluten again, only eating gluten-free at home (and his father's house too) I reckon, but out and about I think he's having his old favorites - sandwiches & sausage rolls!. He had a complete meltdown this evening and afterward when his father and I talked about diet (the meltdown was triggered by something else) he kept muttering under his breath "I'm not Celiac".

This is what I dreaded because on Gluten he really isn't reasonable or calm. The meltdown was shocking - screaming and swearing at his father and I tears rolling down his face and he was hoarse with shouting. Like when a toddler loses it.

We are going back to GP anyway on Tuesday (who seems pretty reasonable and who first suspected celiac)

Are there any Gluten intolerance tests or food allergy tests that can be done?

I'm only chasing a diagnosis of some kind for him because basically he believes the biopsy and the registrar at the hospital and he's not at one with his body or feelings right now cos he gluten up.

Also has anybody had any experience of Vega testing?

ravenwoodglass Mentor

Well, my son is well and truly on gluten again, only eating gluten-free at home (and his father's house too) I reckon, but out and about I think he's having his old favorites - sandwiches & sausage rolls!. He had a complete meltdown this evening and afterward when his father and I talked about diet (the meltdown was triggered by something else) he kept muttering under his breath "I'm not Celiac".

This is what I dreaded because on Gluten he really isn't reasonable or calm. The meltdown was shocking - screaming and swearing at his father and I tears rolling down his face and he was hoarse with shouting. Like when a toddler loses it.

We are going back to GP anyway on Tuesday (who seems pretty reasonable and who first suspected celiac)

Are there any Gluten intolerance tests or food allergy tests that can be done?

I'm only chasing a diagnosis of some kind for him because basically he believes the biopsy and the registrar at the hospital and he's not at one with his body or feelings right now cos he gluten up.

Also has anybody had any experience of Vega testing?

You could try Enterolab testing if it is available in your state. They look for the antibodies in the stool. If he will visit here that might also be helpful.

Igg postive Rookie

Zus888, I had the same question. I found this article by Dr. Crowe Open Original Shared Link where she says that a positive gliadin antibody (without a positive biopsy) points to a person on the way to being a celiac. She then recommends that they go on a gluten-free diet.

LolaK Newbie

Zus888, I had the same question. I found this article by Dr. Crowe Open Original Shared Link where she says that a positive gliadin antibody (without a positive biopsy) points to a person on the way to being a celiac. She then recommends that they go on a gluten-free diet.

I found that really interesting - I have read a couple of similar articles but can't think where (might have been here :-)) which I'll try look out and post,but late here in the UK and off to bed.

Has anyone else had positive blood test followed by negative one or know why this might occur?

LolaK Newbie

Well, we went back to the GP today as my son has been discharged by the gastro consultant as 'better' and no need for further investigations.

I was surprised by his response. He said we can't know at what point Coeliac damage appears in the gut and that the biopsies were taken from only a few places and may have missed damage that was there. He also said there is so much the medical profession don't understand about Coeliac and Gluten problems.

He is going to get back to the consultant and ask him why my son was discharged and then consider sending him to a general consultant (although they are getting rarer here in UK).But he said an official diagnosis is not really necessary if the diet is working, that my son obviously has a problem with gluten even if it can't be 'explained'.

He was disappointed that the Gastro thing had been so unsatisfactory for us and positively supportive of continuing a Gluten free diet.

This was what we needed to hear today and positive reinforcement for the diet for a teenager who was pretty much given permission from the consultant to go back to a normal diet.

ravenwoodglass Mentor

Well, we went back to the GP today as my son has been discharged by the gastro consultant as 'better' and no need for further investigations.

I was surprised by his response. He said we can't know at what point Coeliac damage appears in the gut and that the biopsies were taken from only a few places and may have missed damage that was there. He also said there is so much the medical profession don't understand about Coeliac and Gluten problems.

He is going to get back to the consultant and ask him why my son was discharged and then consider sending him to a general consultant (although they are getting rarer here in UK).But he said an official diagnosis is not really necessary if the diet is working, that my son obviously has a problem with gluten even if it can't be 'explained'.

He was disappointed that the Gastro thing had been so unsatisfactory for us and positively supportive of continuing a Gluten free diet.

This was what we needed to hear today and positive reinforcement for the diet for a teenager who was pretty much given permission from the consultant to go back to a normal diet.

So glad to hear that you had a good appointment with the doctor. Hopefully the doctors words and your son's horrible reaction to going off the diet will be enough reinforcement for him to get back on the diet and stay on it.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,174
    • Most Online (within 30 mins)
      7,748

    stache
    Newest Member
    stache
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.7k

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)

    • There are no registered users currently online

  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Gluten-like cross reactions to other foods are from the proteins that make them up. Dextrose is the sugar component found in corn.
    • Ryangf
      I just found out a few days ago that some salt like table salt contains dextrose that’s derived from corn. I’ve been thinking about getting rid of using table salt and just using my own kosher or Himalayan salt, but tbh I’m reluctant to do it. I’ve cut out a lot of things and I don’t really want to cut out anything else that I’m not sure will effect me…in a super small amount that it might be added to salts to stabilize the iodine. I don’t want to be further alienated when I have to go to a restaurant with my friends. Also most of the items at my house that have salt in it canned food etc. are some of the few quick things I can eat- because I’m not the one paying for the food in my household and i can only ask for so much. I’m not in a place financially where I can get a lot of my specialized items- although my family tries their best to get items I Can actually stand. I get I can bring a my own salt with me at a restaurant and ask for no seasoning but it feels like a lot to me- cause I already check for cross contamination and ask if the food has like a high volume of corn in it like cornstarch etc. I’ve also heard most dextrose is not derived from the Zein (corn gluten) portion of it- so it might be safe- but idk if that’s true. I just wanna know if anyone actually responded to it negatively.
    • Scott Adams
      For my first couple of years after discovering my celiac disease I also had to avoid cow's milk/casein and eggs, as well as other things, but could tolerate duck eggs and sheep and goat's milk products. I'm not sure if you've tried those, but it could be worth testing them out.
    • knitty kitty
      Hello, @Kwinkle, How are you doing?   Have you tried adding a Magnesium supplement?   The B Complex vitamins need magnesium to work properly, especially thiamine vitamin B 1.   Magnesium deficiency symptoms and Thiamine deficiency symptoms both include gas and bloating.  Thiamine deficiency symptoms also include loss of appetite and fatigue.   My gas and bloating resolved rather quickly when I took Benfotiamine (a form of thiamine shown to promote intestinal healing) and Magnesium Glycinate in addition to my B 50 Complex (all twice a day plus the following...).   I found Magnesium L-Threonate or Magnesium Taurate are better when taken with a form of thiamine called TTFD (Tetrahydrofurfuryl dusulfide) because all of these cross the blood brain barrier easily, which corrects the loss of appetite, fatigue and anxiety.    Like @Celiacandme said, keeping a food/mood/poo'd journal is a big help in finding problematic foods, and for making sure your diet is not carbohydrate heavy.  If you're eating a lot if processed gluten free facsimile foods, be aware they do not have vitamins and minerals added to them like their gluten containing counterparts.  For every 1000 kcal of carbohydrates, we need an extra 500 mg of thiamine to turn them into energy and not store them as fat.   Let us know how you're doing!
    • Scott Adams
      Yes, if you had symptoms when eating gluten ruling out celiac disease won't necessarily mean you'll be able to eat gluten again, although it might mean that you may be able to be less strict with your gluten-free diet. 
×
×
  • Create New...