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

Gluten Free Now I'm Ok?


asymmetricOCD

Recommended Posts

asymmetricOCD Newbie

To anyone that can shed a light on my situation please do.

I was first diagnosed with having the H. Pylori bacteria and was medicated for that to get rid of the bacteria. The doctor told me then to try a wheat/gluten free diet to see if I would feel better. He suspected it would because my blood test had come back positive with anti-bodies.

After having been on the diet for a little while, 2 weeks a month maybe I went back for a check up. I was feeling better and he told me then that the wheat/gluten intolerance/allergy could have been the cause of all the mental disorders I had gone through the previous 3 years of my life. It was a big wave of relief and distress because of the horrible anxiety and grief I had been through with the psychiatrists and mental illnesses, but now at least I wasn't crazy.

I've been trying my best and have been 100% reading labels before I eat anything to make sure nothing lies within the food that I can't eat. No maltodextrin until sure of it's source, no artificial flavorings. The doctor had told me that there was a possibility that because the way the wheat/gluten affected me mentally that the serotonin mishap in my brain could cause permanent calcification of my brain to indefinitely alter my brain and/or personality which is an extremely scary thing to think and it makes me even more paranoid about the food I eat.

Today has been about 8 months on a gluten free diet and I just am not feeling all that much better off wheat than I was on it. I ate a few crackers and have felt better! I just ate a slice of wheat-full pizza and feel... great!

Is there a possibility this was a misdiagnosed or proposed notion that I am gluten intolerant or will my stomach continue to feel fine and my brain and other organs slowly rot..?


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



Celiac.com Sponsor (A8-M):



MissPJ Newbie
To anyone that can shed a light on my situation please do.

I was first diagnosed with having the H. Pylori bacteria and was medicated for that to get rid of the bacteria. The doctor told me then to try a wheat/gluten free diet to see if I would feel better. He suspected it would because my blood test had come back positive with anti-bodies.

After having been on the diet for a little while, 2 weeks a month maybe I went back for a check up. I was feeling better and he told me then that the wheat/gluten intolerance/allergy could have been the cause of all the mental disorders I had gone through the previous 3 years of my life. It was a big wave of relief and distress because of the horrible anxiety and grief I had been through with the psychiatrists and mental illnesses, but now at least I wasn't crazy.

I've been trying my best and have been 100% reading labels before I eat anything to make sure nothing lies within the food that I can't eat. No maltodextrin until sure of it's source, no artificial flavorings. The doctor had told me that there was a possibility that because the way the wheat/gluten affected me mentally that the serotonin mishap in my brain could cause permanent calcification of my brain to indefinitely alter my brain and/or personality which is an extremely scary thing to think and it makes me even more paranoid about the food I eat.

Today has been about 8 months on a gluten free diet and I just am not feeling all that much better off wheat than I was on it. I ate a few crackers and have felt better! I just ate a slice of wheat-full pizza and feel... great!

Is there a possibility this was a misdiagnosed or proposed notion that I am gluten intolerant or will my stomach continue to feel fine and my brain and other organs slowly rot..?

I am in a similar situation, although I haven't been off gluten for as long. My biggest difference off gluten was lack of depression, anxiety and my confidence has tripled. I also tried to "gluten" myself, just to see what happened, and I had no gastro symptoms at all. But then over the next week, my mood steadily declined.

Another celiac suggested I may be intolerant to other things, so I'm going to look into that also, could there be something else in your diet that is still holding you back?

I am interested to know how many others are asymptomatic, with mental issues being the main symptom of gluten. I know I am much healthier off gluten, but it's hard to wrap my head around it if I don't have any gastro probs with it.

asymmetricOCD Newbie
I am in a similar situation, although I haven't been off gluten for as long. My biggest difference off gluten was lack of depression, anxiety and my confidence has tripled. I also tried to "gluten" myself, just to see what happened, and I had no gastro symptoms at all. But then over the next week, my mood steadily declined.

Another celiac suggested I may be intolerant to other things, so I'm going to look into that also, could there be something else in your diet that is still holding you back?

I am interested to know how many others are asymptomatic, with mental issues being the main symptom of gluten. I know I am much healthier off gluten, but it's hard to wrap my head around it if I don't have any gastro probs with it.

That's the way it is with me! I can't understand a disease or intolerance that doesn't actually affect me, as it seems. I've been writing down everything I've eaten for a week, while OFF gluten and I just can't seem to find what's affecting me. My stomach seems to do somersaults besides the gluten. I ate the pieces of pizza last night and seem to be fine!

I'm looking at to just get a biopsy and be done with this thing either way if I do or don't have it but I have to worry about pre-existing conditions because my insurance will be changing in the next 6 months.

I wonder how many people have the mental side effect as well, it's a conundrum.

carsondcat Newbie

To anyone that can shed a light on my situation please do.

I was first diagnosed with having the H. Pylori bacteria and was medicated for that to get rid of the bacteria.

I can't answer your questions but (i expect others here can) 25 years ago (took 39 years for a Celiac Diagnosis) I was diagnosed with having the H. Pylori bacteria through a positive blood test and i was treated for it with medication... My symptoms remained after finishing the course of medication and the DR told me i would still experience pain after eating certain foods due to scarring left by the ulcer. When all those years later i had an endoscopy and biopsy for the Celiac diagnosis the GI told me that I had never had an ulcer as it would have been visible via the scope (scarring).. Basically i ignored the tremendous amount of pain i was in because of what the DR said and because of the diagnosis so did the DRs EVERYTIME i went back to see them. In my situation, the H.Pylori bacteria (through a blood test) was one of my misdiagnosis, that was my Celiacs, popping it's head up yet again for the Drs to notice, if only they had diagnosed me then i probably wouldn't have all the other health issues i have now......

asymmetricOCD Newbie

Consondcat,

I'm sorry for your humongous misdiagnosis of the H. Pylori. I'm feeling very lost now and have only been on this journey of diagnosis/misdiagnosis for 4 or 5 years. I was in shock almost when the doctor told me the wheat could have been the cause of my mental issues, I cannot imagine the shock you felt after 25 years!

I found a website that goes into more detail of brain allergies for anyone reading this little topic.

Open Original Shared Link

I found it pretty interesting anyways. Now I'm wondering if I possibly have an allergy to something completely different from gluten that could have caused my mental ordeals. It all started very slowly then progressed rapidly while being put on heavy anti-psychotics so maybe that's a cause. *sigh*

GottaSki Mentor

Did you have any digestive issues before trying gluten-free? If not, it may be that your mental issues were caused by diet but was caught before you had major digestive issues - therefore you wouldn't see a day to day reaction when ingesting gluten -- doesn't mean it won't set you back.

Curious -- did your doctor check your iron, ferritin, b, d, k levels before you went gluten free.

If some or all of these nutrients are low it makes sense that your neurotransmitters may also be low which can cause all sorts of mental & physical problems.

asymmetricOCD Newbie
Did you have any digestive issues before trying gluten-free? If not, it may be that your mental issues were caused by diet but was caught before you had major digestive issues - therefore you wouldn't see a day to day reaction when ingesting gluten -- doesn't mean it won't set you back.

Curious -- did your doctor check your iron, ferritin, b, d, k levels before you went gluten free.

If some or all of these nutrients are low it makes sense that your neurotransmitters may also be low which can cause all sorts of mental & physical problems.

I had few digestive issues that weren't very bad like gas. I've never had many of the bad symptoms until more recently while being gluten free which is completely frustrating. That does make sense though about the doctors catching the mental before digestive. A few of my siblings are lactose intolerant so allergies do run in my family. As well as mental illnesses. My Mom and my Dad's father were adopted though so the family tree only runs with my immediate family pretty much.

Doctor did not test for any of those vitamin deficiencies before suggesting celiacs/gluten free diet. I called him yesterday and he said I won't know anything until I get a biopsy done but that the symptoms will come back while eating gluten.. so I'm not sure if he thinks surely I have it anyways.

I'm stuck as what to do because my insurance is running out in January and I don't get new insurance for another 5 months from now. I want to be sure of what I have but I've heard Celiacs is considered a pre-existing condition. :(

So if I do have gluten-intolerance causing "brain allergy" at least I'm thinking that I don't have to be as meticulous when I eat. I think as long as I don't eat things that obviously have wheat in them I should be fine but I'll start to not worry as harshly about "artificial flavorings" or "spices" maybe as it's a small trace of "possible" wheat.


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



Celiac.com Sponsor (A8-M):



mushroom Proficient
I had few digestive issues that weren't very bad like gas. I've never had many of the bad symptoms until more recently while being gluten free which is completely frustrating. That does make sense though about the doctors catching the mental before digestive. A few of my siblings are lactose intolerant so allergies do run in my family. As well as mental illnesses. My Mom and my Dad's father were adopted though so the family tree only runs with my immediate family pretty much.

Doctor did not test for any of those vitamin deficiencies before suggesting celiacs/gluten free diet. I called him yesterday and he said I won't know anything until I get a biopsy done but that the symptoms will come back while eating gluten.. so I'm not sure if he thinks surely I have it anyways.

I'm stuck as what to do because my insurance is running out in January and I don't get new insurance for another 5 months from now. I want to be sure of what I have but I've heard Celiacs is considered a pre-existing condition. :(

So if I do have gluten-intolerance causing "brain allergy" at least I'm thinking that I don't have to be as meticulous when I eat. I think as long as I don't eat things that obviously have wheat in them I should be fine but I'll start to not worry as harshly about "artificial flavorings" or "spices" maybe as it's a small trace of "possible" wheat.

Something strange going on here. You say you have been gluten free for eight months, had few digestive issues before then, and the doctor now says he can't diagnose you without a biopsy. If you have been gluten free for eight months a biopsy will be useless at this point. You would have to go back on gluten for 2-3 months for a biopsy to be valid, and if your symptoms were primarily mental you may not have any intestinal damage anyway. I gather he did no testing to back up his possible mental diagnosis, like a brain scan for UBO's????(unidentified bright objects) This is the most common symptom/test for those whose brains have been affected by gluten. And if your brain!!! is affected by gluten, you surely do not want to eat it, that's for sure. I think it's time you got a second opinion from someone knowledgeable.

ravenwoodglass Mentor
So if I do have gluten-intolerance causing "brain allergy" at least I'm thinking that I don't have to be as meticulous when I eat. I think as long as I don't eat things that obviously have wheat in them I should be fine but I'll start to not worry as harshly about "artificial flavorings" or "spices" maybe as it's a small trace of "possible" wheat.

Sure as long as you don't mind risking losing the ability to walk a straight line or at all, or you don't mind your brain getting so foggy that you can't think well enough to read or retain info, as long as you don't mind getting on an emotional rollercoaster or even perhaps becomeing incontinent. Then yea if you don't mind those issues and others that can stem from neuro predominant celiac you can be lax on the diet.

IMHO those of us with brain impact need to be just as strict as folks who have severe stomach symptoms. Not less.

asymmetricOCD Newbie
Something strange going on here. You say you have been gluten free for eight months, had few digestive issues before then, and the doctor now says he can't diagnose you without a biopsy. If you have been gluten free for eight months a biopsy will be useless at this point. You would have to go back on gluten for 2-3 months for a biopsy to be valid, and if your symptoms were primarily mental you may not have any intestinal damage anyway. I gather he did no testing to back up his possible mental diagnosis, like a brain scan for UBO's????(unidentified bright objects) This is the most common symptom/test for those whose brains have been affected by gluten. And if your brain!!! is affected by gluten, you surely do not want to eat it, that's for sure. I think it's time you got a second opinion from someone knowledgeable.

Well if I continue eating gluten now for another 2-3 months and then get the biopsy that would work well in the timing of things anyways to wait 2-3 months. I'm so very paranoid about doctors as I've been misdiagnosed with severe diseases in the past all beginning at almost 17 years old.. Hospitalized for various mental psychosis' three times in my life is enough to continue my fear of doctors and their whims. The only time that I've had any kind of brain scan was when I was 16 almost 17 and had some tests done when I started having auditory hallucinations. Then they determined I did not have anything physically wrong with me but that I was schizophrenic. Only a few brain scans and simple blood tests for "physical" out the door.

asymmetricOCD Newbie
Sure as long as you don't mind risking losing the ability to walk a straight line or at all, or you don't mind your brain getting so foggy that you can't think well enough to read or retain info, as long as you don't mind getting on an emotional rollercoaster or even perhaps becomeing incontinent. Then yea if you don't mind those issues and others that can stem from neuro predominant celiac you can be lax on the diet.

IMHO those of us with brain impact need to be just as strict as folks who have severe stomach symptoms. Not less.

It's very scary and I'm so paranoid if I'm eating wheat or not and it makes me feel bad when I'm constantly asking people if they cooked my food right.. such as my Mom or something. Thank you for your reply and the straight forward look at the complications that could be caused by this. Do you know if it's mostly gluten that is the cause of brain allergies or could it possibly be something else besides or in addition?

ravenwoodglass Mentor
It's very scary and I'm so paranoid if I'm eating wheat or not and it makes me feel bad when I'm constantly asking people if they cooked my food right.. such as my Mom or something. Thank you for your reply and the straight forward look at the complications that could be caused by this. Do you know if it's mostly gluten that is the cause of brain allergies or could it possibly be something else besides or in addition?

You don't have a brain 'allergy' what you have is the gluten antibodies attacking your brain. If you have the antibodies, which you do if you had a postive test for celiac, you need to stop the antibodies from forming and the way to do is that is being very strict with the diet. The best way to ease your fear with eating food your Mom cooks, or anyone else for that matter is to get them educated about celiac. Can you bring her here to read some posts? That may help. You need to have as clean of a diet as you can, try to eat mostly whole unprocessed foods, meats, veggies, fruits, rice, potatoes, eggs etc.

Gluten can cause many brain issues, from the ataxia (issues with balance), to depression, anxiety and more. It can take time for healing to take place although some see resolution fairly quickly. There are of course times when mental issues are being caused by a combination of gluten and other factors in celiacs. But many will see a great deal of improvement after they have healed and the antibodies have stopped their attack.

asymmetricOCD Newbie
You don't have a brain 'allergy' what you have is the gluten antibodies attacking your brain. If you have the antibodies, which you do if you had a postive test for celiac, you need to stop the antibodies from forming and the way to do is that is being very strict with the diet. The best way to ease your fear with eating food your Mom cooks, or anyone else for that matter is to get them educated about celiac. Can you bring her here to read some posts? That may help. You need to have as clean of a diet as you can, try to eat mostly whole unprocessed foods, meats, veggies, fruits, rice, potatoes, eggs etc.

Gluten can cause many brain issues, from the ataxia (issues with balance), to depression, anxiety and more. It can take time for healing to take place although some see resolution fairly quickly. There are of course times when mental issues are being caused by a combination of gluten and other factors in celiacs. But many will see a great deal of improvement after they have healed and the antibodies have stopped their attack.

Well I think the thing I need to do (now that I've learned my insurance-to-be does not case "pre-existing" conditions) is to get surely tested for the gluten-antibodies. I've been writing down many things to ask the doctor when I go in a few days. I would have to be on a a diet with gluten for 2-3 months before it would be accurate to have a biopsy done?

Thank you!

ravenwoodglass Mentor
I would have to be on a a diet with gluten for 2-3 months before it would be accurate to have a biopsy done?

Thank you!

Yes although if you become ill from the challenge that is a valid diagnosis also. I would suggest when you go back on gluten for the first week challenge it with something like cream of wheat or triscuits for that first week. If you go back to gluten by all of a sudden eating stuff like fast food and pizza you may feel a bit of confusion wondering if it was the gluten or a sudden increase in greasy or spicy food.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,542
    • Most Online (within 30 mins)
      7,748

    Jacqueline Dee
    Newest Member
    Jacqueline Dee
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
    • Celiac50
      That sounds so very likely in my case! I will absolutely ask my doctor on my next bone check coming up in March... Thanks a lot! 
    • trents
      Calcium levels as measured in the blood can be quite deceiving as the body will rob calcium from the bones to meet demands for it by other bodily functions. Also, supplementing with calcium can be counterproductive as it tends to raise gut pH and decrease absorption. More often than not, the problem is poor absorption to begin with rather than deficiency of intake amounts in the diet. Calcium needs an acidic environment to be absorbed. This is why so many people on PPIs develop osteoporosis. The PPIs raise gut pH. And some people have high gut PH for other reasons. Low pH equates to a more acidic environment whereas high pH equates to a more basic (less acidic) environment.
    • Celiac50
      Kind thanks for all this valuable information! Since my Folate was/is low and also my Calcium, there IS a chance I am low in B vitamins... My doctor only measured the first two, oh and Zinc as I has twisted her arm and guess what, that was mega low too. So who knows, until I get myself tested properly, what else I am deficient in... I did a hair mineral test recently and it said to avoid All sources of Calcium. But this is confusing for me as my Ca is so low and I have osteoporosis because of this. It is my Adjusted Ca that is on the higher side and shouldn't be. So am not sure why the mineral test showed high Ca (well, it was medium in the test but relative to my lowish Magnesium, also via hair sample, it was high I was told). But anyway, thanks again for the VitB download, I will look into this most certainly!
×
×
  • 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.