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 Celiac.com!
    eNewsletter
    Donate

Gluten Free Since 2010 And Still Suffering.


Celiacsuffer09

Recommended Posts

Celiacsuffer09 Newbie

Hello everyone. I'm new to the forums and I'm here looking for some support. I was diagnosed at the age of 29 in February of 2009 with Celiac disease. The diagnoses was by blood work alone and I started the gluten-free diet right away. In May of that year I become really ill and was sent in for a scope procedure. The biopse came back negative for Celiac disease so I started eating gluten again, but the smytoms was still there. I was still having frequent bowel movements, diarrhea, sudden urgency to have a bowel movements and so fourth. So I went back and had the scope procedure done again and the biopse showed Celiac disease. I started the diet once again and have been gluten-free since March 2010.

Since being gluten-free I have seen some improvement, but to this day I still have digestive issues. Like today, I have had 7 bowel movements. I'm doing everything to keep gluten out of my diet, I exercise a lot and trying to be healthier. In the past year alone I have had 2 scope procedures done and things come back looking good. No blunting of the villi or any signs of other diseases. Some days I feel so lost and don't really know what to be eating anymore.

The doctor recommended taking a fiber supplement, that didn't help. He recommended 2 different medications for IBS, which I tried both with no affect. I was tested for lactose intolerence which came back negative. I just don't know what to be doing.

I do have other health issues. I have been battling depression since 2010 and I have back issues. I question if these other issues are having a impact on my digestive problems. I was wondering what other health issues my fellow Celiac suffers have? I am also looking for advice and help in regards to my digestive issues. I would like to know if you all are still having issues while being gluten-free? When the GI doc tells you there isn't much more that he can do for you, you feel alone and question if you will ever get better.

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



NoWhammies Newbie

I'm sorry you're still struggling. Have you ever tried the low-FODMAP plan for IBS? The four-week elimination diet can help you determine if perhaps certain types of carbohydrates are causing some of your symptoms. It's pretty restrictive, but it's only four weeks. Also, do others in your home eat gluten/prepare foods with gluten? I wonder if you are dealing with cross contamination issues.

Link to comment
Share on other sites
cyclinglady Grand Master

How is your gallbladder? Still functioning? Any other food intolerances?

Link to comment
Share on other sites
Dugudugu Rookie

I was also tested for lactose intolerance and the test came back negative, just like the gluten, soy but also cats and dog allergies. If I eat a slice of cheese or sleep with a cat beside my pillow, I'll know immidiately. So for me the test has no value and I recomment to go lactose-free afteral for some time and give it a try.

Currently I am having the same issues as you have. My docter has send me in for a colonscopy as he wants to make sure the problem is not there. I still have to find the courage to make the appointment....

Link to comment
Share on other sites
ravenwoodglass Mentor

Are you taking any meds for the other conditions? If so have you checked to be sure that they are gluten free?  Have you tried eliminating all dairy and soy? Some of us have problems with those and casien (milk protein) intolerance wouldn't show up on lactose testing. Be sure to check out the newbie thread at the top of the Coping thread just in case there is something that is CCing you. Considering how much gluten we have to consume to be tested after being gluten free it might be possible that you are being CC'd but not at a high enough level to show up on testing. 

I hope you can get to the bottom of what is going on soon. 

Link to comment
Share on other sites
C-Girl Contributor

Hello everyone. I'm new to the forums and I'm here looking for some support. I was diagnosed at the age of 29 in February of 2009 with Celiac disease. The diagnoses was by blood work alone and I started the gluten-free diet right away. In May of that year I become really ill and was sent in for a scope procedure. The biopse came back negative for Celiac disease so I started eating gluten again, but the smytoms was still there. I was still having frequent bowel movements, diarrhea, sudden urgency to have a bowel movements and so fourth. So I went back and had the scope procedure done again and the biopse showed Celiac disease. I started the diet once again and have been gluten-free since March 2010.

Since being gluten-free I have seen some improvement, but to this day I still have digestive issues. Like today, I have had 7 bowel movements. I'm doing everything to keep gluten out of my diet, I exercise a lot and trying to be healthier. In the past year alone I have had 2 scope procedures done and things come back looking good. No blunting of the villi or any signs of other diseases. Some days I feel so lost and don't really know what to be eating anymore.

The doctor recommended taking a fiber supplement, that didn't help. He recommended 2 different medications for IBS, which I tried both with no affect. I was tested for lactose intolerence which came back negative. I just don't know what to be doing.

I do have other health issues. I have been battling depression since 2010 and I have back issues. I question if these other issues are having a impact on my digestive problems. I was wondering what other health issues my fellow Celiac suffers have? I am also looking for advice and help in regards to my digestive issues. I would like to know if you all are still having issues while being gluten-free? When the GI doc tells you there isn't much more that he can do for you, you feel alone and question if you will ever get better.

 

First: your doctor diagnosed you with celiac, you went gluten free for a few months and the biopsy was negative... and your doctor ignored the blood positive? If I were you, I'd get a new doctor! You ate gluten for almost a year and duh! You have damage to your small intestine. That just doesn't make any sense for a doctor to let you go through that.

 

Rather than your depression causing digestive issues, I would hazard a guess that your digestive issues are causing your depression. There have been Open Original Shared Link that support the idea, although other studies comparing depression rates in the celiac vs. general population didn't detect a difference.

 

I was diagnosed with microscopic colitis half a year after going gluten free, the lingering symptoms were taking a huge toll on my mental health. Once I was treated for the MC, my mental state became immediately better.

 

The MC Open Original Shared Link in the celiac population is 50x that of the regular folks, so it's worth getting checked out. It involves a colonoscopy with numerous biopsies up and down the colon, unfortunately.

 

Best of luck, hope you get some answers.

Link to comment
Share on other sites
Celiacsuffer09 Newbie

I have looked into the Fodmap diet a few months ago. I think I may have to give it a try. I was questioning if I may have been getting cross contaminated by others I have lived with, but right now I'm living on my own and still having the issues. 

I'm sorry you're still struggling. Have you ever tried the low-FODMAP plan for IBS? The four-week elimination diet can help you determine if perhaps certain types of carbohydrates are causing some of your symptoms. It's pretty restrictive, but it's only four weeks. Also, do others in your home eat gluten/prepare foods with gluten? I wonder if you are dealing with cross contamination issues.

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



Celiacsuffer09 Newbie

I think the doctor has tested my gallbladder, so I guess it's ok. As for other food intolerances, I have only been tested for lactose intolerance, so I'm unaware of any others.

How is your gallbladder? Still functioning? Any other food intolerances?

Link to comment
Share on other sites
Celiacsuffer09 Newbie

I have reduced my dairy intake dramatically from my diet. I switched to a Soy beverage to replace milk. I have tried eliminating all dairy from my diet before, with no real results.

I was also tested for lactose intolerance and the test came back negative, just like the gluten, soy but also cats and dog allergies. If I eat a slice of cheese or sleep with a cat beside my pillow, I'll know immidiately. So for me the test has no value and I recomment to go lactose-free afteral for some time and give it a try.

Currently I am having the same issues as you have. My docter has send me in for a colonscopy as he wants to make sure the problem is not there. I still have to find the courage to make the appointment....

Link to comment
Share on other sites
Celiacsuffer09 Newbie

I'm taking medications for my depression and hypertension, in which I always check with the pharmacy to ensure they are gluten-free. 

Are you taking any meds for the other conditions? If so have you checked to be sure that they are gluten free?  Have you tried eliminating all dairy and soy? Some of us have problems with those and casien (milk protein) intolerance wouldn't show up on lactose testing. Be sure to check out the newbie thread at the top of the Coping thread just in case there is something that is CCing you. Considering how much gluten we have to consume to be tested after being gluten free it might be possible that you are being CC'd but not at a high enough level to show up on testing. 

I hope you can get to the bottom of what is going on soon. 

Link to comment
Share on other sites
Celiacsuffer09 Newbie

My family doctor had diagnosed me with the blood work, but the GI doctor who took the biopsies basically ignored the blood work. In regards to the depression, I know a lot of that is from my digestive issues, but wonders some days is it the opposite. 

 

In regards to other GI diseases, I have had several scopes up and down and biopsies taken. No other diseases was found. 

First: your doctor diagnosed you with celiac, you went gluten free for a few months and the biopsy was negative... and your doctor ignored the blood positive? If I were you, I'd get a new doctor! You ate gluten for almost a year and duh! You have damage to your small intestine. That just doesn't make any sense for a doctor to let you go through that.

 

Rather than your depression causing digestive issues, I would hazard a guess that your digestive issues are causing your depression. There have been Open Original Shared Link that support the idea, although other studies comparing depression rates in the celiac vs. general population didn't detect a difference.

 

I was diagnosed with microscopic colitis half a year after going gluten free, the lingering symptoms were taking a huge toll on my mental health. Once I was treated for the MC, my mental state became immediately better.

 

The MC Open Original Shared Link in the celiac population is 50x that of the regular folks, so it's worth getting checked out. It involves a colonoscopy with numerous biopsies up and down the colon, unfortunately.

 

Best of luck, hope you get some answers.

Link to comment
Share on other sites
beth01 Enthusiast

For other food intolerances, you are going to have to keep a food diary. Write down everything you eat and drink and your symptoms when you get them so you can pinpoint the problem foods. Soy makes me feel like gluten does, cut out the soy milk and try an almond milk. Most likely the pharmacy isn't going to tell you about each an every med, you usually have to call the manufacturer, just my experience. Good luck and hope you feel better.

Link to comment
Share on other sites
cap6 Enthusiast

RE: meds......   If you can get your doctor to write your prescription out with "gluten free" on it the pharmacy will pay attention and be sure that the medication is ok.  If it's part of the prescription then they have to pay attention.  

Link to comment
Share on other sites
BoJonJovi Newbie

It is likely that you are still eating out or are taking some medications or supplements that have gluten. Tighten er up partner and eat at home. 

 

It takes 1/200th of a teaspoon of gluten to set off the autoimmune response. If you remember that you can see the issue of eating out. If they have gluten fair it is likely that you are going to get some of it from an inexperienced cook or server. Eating out is a crap shoot at best. Frankly I would rather shoot craps, lose money than be sick. 

Link to comment
Share on other sites
JaneWhoLovesRain Enthusiast

Hi - I'm wondering if you are eating anything that has the ingredients sorbitol  or manitol or inulin.  These give me terrible stomach and intestinal cramping and diarreah and nausea.  They are right at the top of my do not eat list along with gluten.

 

Edited to add - xanthan gum can do it also and unfortunately it's in a lot of gluten-free food as well as non gluten-free food.

Link to comment
Share on other sites

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - plumbago replied to Suzi374's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      Lots of tests

    2. - trents replied to Suzi374's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      Lots of tests

    3. - Suzi374 replied to Suzi374's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      Lots of tests

    4. - Suzi374 posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      Lots of tests

    5. - Peace lily posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      0

      Would like to gain weight


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,224
    • Most Online (within 30 mins)
      7,748

    Suzi374
    Newest Member
    Suzi374
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • plumbago
      I'm also a nurse, but one who has worked in chronic care, and to some extent, it is more satisfying to see patients through to a diagnosis (as opposed to working in the ED), but an accurate diagnosis does not occur not as often as it should! Your posting presents a lot of information. But a couple of things I can respond to. One, celiac disease is diagnosed by endoscopy and biopsy of the duodenum. So, pathology will need to weigh in. It's not diagnosed on gastroscopy. (At least, not as far as I know). Two, did you get blood tests for celiac disease? You will need to be eating gluten in order for those to be accurate. Three, where was the CT angiogram (of what)? I could go on and on, but thought I'd start there.
    • trents
      Was a biopsy done when you had your gastroscopy? Concerning your anemia, are you B12 deficient? It's nearly impossible to get sufficient B12 if you are a vegetarian unless you take supplements.
    • Suzi374
      And I’m anaemic, however I’m also female and vegetarian. I had an iron trans a couple of years ago however it’s starting to dwindle and taking supplements doesn’t seem to work. I can’t seem to absorb it. 
    • Suzi374
      Hi, I attended a neurologist appt last Tuesday, which I nearly cancelled, due to ongoing numbness and tingling in toes to mid foot. One of the first things he asked was ‘are you celiac’. I’m not. He thought all reflexes were ok but at the last minute decided on nerve conduction tests which were low normal. He was a little confused as he felt they should be better and tried a new set of probs, all the time, giving me multiple shocks which were not enjoyable lol. Anyway, he’s now ordered tests for myeloma, and all the vitaminy things that so many of you mention on here, also tests looking for autoimmune responses. I already have Hashimotos. Interestingly, to me, but maybe someone out there can relate or knows more than i do, although I was a nurse, but ED not ‘weird symptoms’  nurse. Anyway back to the interesting thing, I took duramine in 2013 to lose weight which caused a massive panic attack when I stopped taking it and half my hair fell out. I only took it for a week but it was horrible and I regret it. It triggered ongoing panic attacks which are horrendous. So I feel like I’m a bit crazy. Then in 2020 I had this sudden onset of horrible pain when trying to eat a cinnamon roll. It continued and I lost around 20 kgs. I had two gastroscopes and a colonoscopy and they were all normal. I scored a barium swallow and CT angiogram. All normal. The pain subsided a little but I was left with reflux and an awful feeling that I couldn’t get air when I ate some foods. This was not anxiety.  The anxiety was separate and I still maintain this. This was something to do with eating. It was like the air was thick but I wasn’t short of breath. I just had the sensation I was, then it triggered anxiety. Anyway, I had other weird things- couldn’t bend knees to shave legs in shower lol. Knees felt stiff and swollen but they weren’t. Knee WOUld swell up randomly but mri showed minimal issues. A bit of a meniscus degeneration but insignificant. Then the buzzing sensations in my head, the feeling like someone was stabbing me with something sharp. So now, I pre empted his tests, although I don’t think I’m celiac because it should have come up on gastroscopy, I’ve gone off gluten. Since Tuesday last week so 9 days. Since then I don’t appear to be as constipated, I realised I got through today without a nap and I’m not tired, maybe it’s just today and not related but I get very tired normally and sleep straight after work often, I can bend my knees and shave my legs lol, the buzzing vibrating has gone from my head, I had to call and ambulance as my heart decided we were off on a run, but we weren’t running and I’ve been a bit twitchy at bed time when trying to sleep, reflux is improving, I did get the weird suffocating feeling a bit when eating today but not as bad normall. Tingling and numbness still present and I felt like it moved up my legs a bit today but I’m a bit jittery. So I don’t know if it’s celiac disease or a gluten intolerance but I think, and it may be wishful thinking because my symptoms do make life a bit challenging, but maybe I’m feeling better. I don’t feel as cloudy. My thinking feels crisper. Like there’s no buzzing and I’m not fighting to break through the cloudiness now. I hope so much that this may help me feel a bit better moving forward. It would be a miracle as I really have struggled to work and parent and keep the house clean and I’m always anxious and exhausted.  If you get this far, please tell me if you you can relate to any of the above. Oh and tonsils out 5 years ago but before that antibiotics multiple times a year, sometimes intramuscular because they were so bad.  Op was meant to take 30 mins, it took 1.5 hours due to size of them. 
    • Peace lily
      Im still not gaining weight I’m on a gluten free diet . And still having issues with constapation started priobiocs figured it would help been over two weeks . I guess it’s going to be a long road for me .
×
×
  • Create New...