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

Biopsy Results Within Normal Limits?


Perthgirl

Recommended Posts

Perthgirl Newbie

Hi new to this forum and feeling confused...

Been seeing a GI/Hepatologist for 6months with liver problems. Lots of leisions of different kinds.. He did full blood tests of everything... Came back with extremely iron deficient. He felt it was so low there must be a reason behind it (bleeding somewhere) and recommended a colonoscopy and endoscopy.

Due to me already having a 3 day stay in hospital earlier in the year with diverticulitis infection and having already gone down the colonoscopy route with the surgeon I was under with no outstanding problems, just diverticulitis, we just did the endoscopy..

The GI's thoughts were ulcer or celiac.. This is when I thought things started to make sense because I had been having many GI problems for awhile and I do have an uncle and aunty who are celiac. We did the endoscopy five weeks ago and have finally got results as "within normal limits". I had had way enough of all the stomach problems I was having, toilet 4 or 5 times a day, noisy stomach, bloated to the point people on the train offered me seats thinking I was pregnant.. so I stopped eating wheat and trying to avoid gluten.. seen a marked improvement..

The other thing is my Aunt believes I could not be celiac because I am very overweight and my cholestrol is sooo high 8.1.. Any advise please I feel like I'm spinning in circles... :(


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



Celiac.com Sponsor (A8-M):



lizard00 Enthusiast

Welcome to the Forum!! You will find lots of support here!!

Sorry to hear about all of your struggles! The tests for Celiac are pretty notorious for being negative. And even with an endoscopy, a biopsy can miss the part of your intestine that has been affected. There's 22 ft (if memory serves me correctly) of small intestine, so that's a possiblity. Have you actually seen the results of your tests? I would suggest you get a copy, if possible.

And there's a large percentage of Celiacs who are actually overweight, not under. It's the whole "starvation" thing. When your body thinks its starving, because it's not absorbing many of the nutrients, then it hangs on to anything that is does get... hence the weight issue. I bet if you remain gluten-free you'll begin to start losing weight.

How long did you go gluten-free and are you still? If you saw marked improvement, stick with it. Dietary response is just as valid as any test. Many of us are self diagnosed (myself included) because of inconclusive tests, but we know that gluten is poison to us. So, I would encourage you to remain gluten-free for longer and just watch things get better!!! :D

RiceGuy Collaborator

I agree completely with lizard00's comments. So I'll just add my encouragement to stick with the diet, and see how much better you feel. And yes, the extra weight might easily diminish as your recovery progresses.

Welcome to the board!

ravenwoodglass Mentor

The diet is the truest test there is. Stick with it and welcome.

skichikk18 Rookie

I also was not officially diagnosed by the doctor. I had so many tests done becuase of over year straight of diaharria. My endoscopy came back negative as did my blood test. My mom has crohns disease and we thought maybe that but every test they did, and they did a lot, came back negative. He suggested trying a gluten free diet to see how I felt. After about 2 weeks on it I felt great and have been gluten free since Jan 1. I dont have the diaherria anymore and no more crazy bad stomach pain and cramping. My hair stopped falling out and i stopped losing weight. Before I went gluten free I was bairly eating because everything went straight through me (5-10 times a day in the bathroom). I go back to my dr in March to see what he has to say, but I feel so much better on this diet I wouldn't imagine he would have me stop. I finally have energy again also, it is great. I am also hoping this will help me get pregnant as I have been seeing a specialist for about 2 1/2 years for that also.

Perthgirl Newbie

Thankyou so much for the warm welcome and encouragement... :)

I have only been following the diet for a couple of weeks but have felt such a marked improvement I have decided to keep going despite the results of the biopsy as I do not want to go back to how I was feeling before.. I have gone from going to the toilet 5-6 times a day to only the once a day, which I cannot remember having been like that for years!!! and my stomach is not as bloated up as it has been and the cramping and noisy stomach has improved. My energy levels are still a struggle but with my iron so low I am prepared it could take some time to get those back up..

I am glad I found this forum which is full of such wonderful information and support... :D

ravenwoodglass Mentor
Thankyou so much for the warm welcome and encouragement... :)

I have only been following the diet for a couple of weeks but have felt such a marked improvement I have decided to keep going despite the results of the biopsy as I do not want to go back to how I was feeling before.. I have gone from going to the toilet 5-6 times a day to only the once a day, which I cannot remember having been like that for years!!! and my stomach is not as bloated up as it has been and the cramping and noisy stomach has improved. My energy levels are still a struggle but with my iron so low I am prepared it could take some time to get those back up..

I am glad I found this forum which is full of such wonderful information and support... :D

Glad to hear you are listening to your body. You should think about getting some sublingual B12, that should help a great deal with energy and other issues. So happy to hear you are on your way to recovery!


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



Celiac.com Sponsor (A8-M):



ksymonds84 Enthusiast
Thankyou so much for the warm welcome and encouragement... :)

I have only been following the diet for a couple of weeks but have felt such a marked improvement I have decided to keep going despite the results of the biopsy as I do not want to go back to how I was feeling before.. I have gone from going to the toilet 5-6 times a day to only the once a day, which I cannot remember having been like that for years!!! and my stomach is not as bloated up as it has been and the cramping and noisy stomach has improved. My energy levels are still a struggle but with my iron so low I am prepared it could take some time to get those back up..

I am glad I found this forum which is full of such wonderful information and support... :D

welcome to the board! I am glad you are staying with the diet. IMO the diet is the best diagnostic tool when other tests are questionable. I am also enjoying the one trip a day to bathroom :D

kathy

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,187
    • Most Online (within 30 mins)
      7,748

    Kris46
    Newest Member
    Kris46
    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

    • Ginger38
      So I recently had allergy testing for IGE antibodies in response to foods. My test results came back positive to corn, white potatoes, egg whites. Tomatoes, almonds and peanuts to name a few.  I have had obvious reactions to a few of these - particularly tomatoes and corn- both GI issues. I don’t really understand all this allergy versus celiac stuff. If the food allergies are mild do I have to avoid these foods entirely? I don’t know what I will eat if I can’t  have corn based gluten free products 
    • Kris2093u4
      Geography makes a difference.  I'm in the West and Trader Joe's gluten-free bread tastes great and is a better price than most gluten-free breads sold elsewhere in my area.  
    • JForman
      We have four children (7-14 yo), and our 7 year old was diagnosed with NCGS (though all Celiac labs were positive, her scope at 4 years old was negative so docs in the US won't call it celiac). We have started her on a Gluten Free diet after 3 years of major digestive issues and ruling out just about everything under the sun. Our home and kitchen and myself are all gluten-free. But I have not asked my husband/her dad or her other siblings to go completely gluten-free with us. They are at home, but not out of the home. This has led to situations when we are eating out where she has to consistently see others eating things she can't have and she has begun to say "Well, I can't have <fill in the blank>...stupid gluten."  How have you supported your gluten-free kiddos in the mental health space of this journey, especially young ones like her. I know it's hard for me as an adult sometimes to miss out, so I can't imagine being 7 and dealing with it! Any tips or ideas to help with this? 
    • Jane878
      By the time I was 5 I had my first auto0immune disorder, Migraine headaches, with auras to blind me, and vomiting, sensitivity to light and sound. I was 5 years old, and my stepfather would have pizza night, milling his own flour, making thick cheesy gluten pizza, that I would eat and the next day, I would have serious migraines, and my mother & stepfather did nothing about my medical problems. When I was 17 in my first year at college, I was diagnosed with my 2nd known auto-immune disorder, Meniere's disease. I was a elite athlete, a swimmer, and soccer player. And once again my parents didn't think anything of understanding why I had a disorder only older people get. Now after my mother passed from Alzheimer's disease she also suffered with living with gluten. She had a rash for 30 years that nobody could diagnose. She was itchy for 45 years total. My brother had a encapsulated virus explodes in his spleen and when this happened his entire intestines were covered with adhesions, scar tissue and he almost lost his life. He has 5 daughters, and when I finally was diagnosed after being pregnant and my body went into a cytokine storm, I lost my chance to have children, I ended up having Hashimoto's disease, Degenerative Disc disease, and my body started to shut down during my first trimester. I am 6ft tall and got down to 119lbs. My husband and I went to a special immunologist in Terrace, California. They took 17 vials of blood as we flew there for a day and returned home that evening. In 3 weeks, we had the answer, I have Celiac disease. Once this was known, only my father and husband made efforts to change their way of feeding me. At the family cabin, my stepfather & mother were more worried that I would ruin Thanksgiving Dinner. It wasn't until one of my cousins was diagnosed with Celiac disease. They finally looked into getting Gluten Free flour and taking measures to limit "gluten" in meals. He did nothing but ask for me to pay for my own food and wi-fi when I came to the cabin to stay after our house burned down. When he informed my mother, they proceeding to get into a physical fight and she ended up with a black eye. The is just more trauma for me. Sam had no interest in telling the truth about what he wanted. He lied to my mother that he had asked my husband if I could pay for "food" when he asked Geoffrey if I had money to pay for my wi-fi. My mother hates when he spends so much time on the computer so he lied and said I could pay for my own food. I will remind you I weighed 119lbs at this time. (At 6ft) that is a very sick looking person. Neither parent was worried about my weight, they just fought about how cheap my stepfather was. As my mother was diagnosed with Alzheimer's disease in 2014. He had her sign over the will to a trust and added his children. He had no testimonial capacity at the time, so she signed without proper papers. Making this Trust null and void. When I gave my brother my childhood home, my mother stated I would be getting an equal part of inheritance to the house on Race. It currently worth 2.0 million $. I got nothing, and my stepfather has since disowned me b/c of my claim and he knows that my mother would never have left it uneven between my biological brother and myself. She sat me and my husband down, as we lived at the Race Street house and treated and took care of it as our own. My brother took over b/c he was going through a horrific divorce and needed a home so he could get a better custody deal with his soon to be ex-wife who was a Assist DA for Denver. She used the girls against him, and he & I were the primary caregivers. We, Judd and I spent the most time with them pre the divorce. Once Judd moved into the house, he threw all of my mother, grandmother and my family heirlooms out to the Goodwill. Nobody told my mother about this as she was going through cancer treatment and had Alzheimer's disease in her mother and her sister. My stepfather and biological brother took advantage of this matter, as I called a "family council" that my brother just never could make it to at the last moment. All of the furnishing, kitchen ware, everything was in the house my brother just moved into. He had had 2 weddings, I chose to elope b/c my stepfather ruined my brother's first wedding by talking about his relationship with my brother in front of my dad and his entire family, insulting him and having my grandfather leave the ceremony. It was a disaster. My stepfather just plays dumb and blames my father for the slight. I was the only child not to have a wedding. So, my mother and stepfather never had to pay for a thing. My mother had had an agreement with my father he'd pay for college and all medical issues with their kids, myself and Judd. So truly my mother never had to pay for anything big for me in her entire life. I am looking for anyone that has had a similar story, where they grew up in a household that had a baker that regularly milled flour and ate gluten. What happened to you? DId you suffer from different auto-immune diseases b/c of living with a baker using "gluten" Please let me know. I have been looking into legal ways to get my stepfather to give me what my mother had promised, and he erased. Thank you for listening to my story. Jane Donnelly  
    • trents
      Possibly gluten withdrawal. Lot's of info on the internet about it. Somewhat controversial but apparently gluten plugs into the same neuro sensors as opiates do and some people get a similar type withdrawal as they do when quitting opiates. Another issue is that gluten-free facsimile flours are not fortified with vitamins and minerals as is wheat flour (in the U.S. at least) so when the switch is made to gluten-free facsimile foods, especially if a lot of processed gluten-free foods are being used as substitutes, vitamin and mineral deficiencies can result. There is also the possibility that she has picked up a virus or some but that is totally unrelated to going gluten-free.
×
×
  • Create New...