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

Help-I Think I'm On To Something Here!


MizzyLou

Recommended Posts

MizzyLou Newbie

Hello - I am a 38 year old female, who has been struggling with digestive issues for 4 years.  My symptoms include loose stools/diarrhea and a constantly grumbling stomach.  I have had a colonoscopy, endoscopy, blood work, and a hida scan.  Everything has come back fine except for the endoscopy, which revealed some mild inflammation of the lining of my stomach (gastritis).  I had always been perfectly healthy, no allergies of any sort, and absolutely no digestive issues until 4 years ago.  It began with an upper abdominal attack (severe pain that came in waves), that led me to the ER.  They suspected gallbladder, but after ultrasound revealed no stones, they sent me home to die as far as I'm concerned.  I was fine the next day and brushed it off as some crazy gastritis or something.  Two months later I had another attack.  This attack was worse and along with the severe pain, I had terrible diarrhea.  I didn't go to the hospital for fear they would send me home again, and just kept thinking that if I could make it through the night, I would be ok.  This wasn't the case.  The pain went away after that night but the severe diarrhea continued for weeks.  It wasn't until I thought I saw blood that I went to my doctor.  He ordered a stool sample, which came back normal.  At one point during this episode, I pooped solid enough to notice that one time, and one time only, the poop was white.  Pure white.  After several weeks of uncontrollable diarrhea, it subsided and what I am left with now is loose stool, every day.  After talking to a friend last week, and telling her I was about to jump off a bridge because of this (not really, but want you to understand the level of frustration), she suggested I follow the blood type diet.  I had bought the book years ago and dug it out the next day.  After looking it over I decided that just about the only thing I was eating everyday was gluten.  I decided to go gluten free.  After two days my stools were almost normal.  It has been a week now, and Iast night was the first time I ate a meal (gluten free) where I felt like I was really eating in four years.  I know that sounds strange, but something inside is different.  I can't explain it properly, but it's almost as if I can eat without reserve now.  What hasn't stopped is the noisy stomach that's driving me crazy.  My question is, has anyone developed this due to an attack of some sort.  I have read that pancreatitis and Celiac go together.  I am wondering if it was a case of pancreatits.  I am also wondering, since I was pregnant during the last four years and my symptoms got better during pregnancy, if the doctor who performed the endoscopy may have missed Celiac.  I know you can be intolerant of gluten and not have Celiac. Thanks for any replies.


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



Celiac.com Sponsor (A8-M):



bartfull Rising Star

Unless the doctor did a biopsy during the endoscopy, he didn't test you for celiac. But whether you have celiac or NCGI, you haven't been gluten-free long enough to see complete healing. Also, for the first two or three weeks you will probably have gluten withdrawal, and a rumbing stomach is not uncommon (along with hunger, headaches, mood swings, and other unpleasant symptoms).

 

You are obviously on the right track. Read the Newbie 101 thread and you will learn about how to avoid cross-contamination. Ask lots of questions. Check out the breakfast/lunch/dinner threads for meal ideas.

 

Welcome to the forum! I'm sorry it took so long for any of us to reply, but we're glad you're here and will help you in any way we can. :)

MizzyLou Newbie

Unless the doctor did a biopsy during the endoscopy, he didn't test you for celiac. But whether you have celiac or NCGI, you haven't been gluten-free long enough to see complete healing. Also, for the first two or three weeks you will probably have gluten withdrawal, and a rumbing stomach is not uncommon (along with hunger, headaches, mood swings, and other unpleasant symptoms).

 

You are obviously on the right track. Read the Newbie 101 thread and you will learn about how to avoid cross-contamination. Ask lots of questions. Check out the breakfast/lunch/dinner threads for meal ideas.

 

Welcome to the forum! I'm sorry it took so long for any of us to reply, but we're glad you're here and will help you in any way we can. :)

Thank you so much for your reply.  I have been learning a lot these past few days.  I have a couple questions if you don't mind...I am almost positive that the doctor did not do a biopsy.  He didn't even talk to me afterward, only to my husband, who said he was more focused on the colonoscopy part of the exam.  I am going to ask my doctor to obtain a report of the endoscopy to make sure, but in the event that he didn't, how long do you think I can remain gluten free and still have testing done?  I know that's a magic question, but everything I've read talks about months.  Do you think if I've been free for weeks I would still test positive?  Also, I have had awesome bowel movements since starting gluten free, then today I had some loose stool.  Is it normal to have relapses like this?  I know it's too early to tell, but I'm afraid that it was a fluke, although I haven't ever had that much improvement in four years!  I'm sure I have been getting small amounts of gluten as my kitchen, and family for that matter, are not gluten free.  Could it be that my body has gotten over the initial shock of going gluten free and it's returning to it's same old self?  Do most people who experience a dramatic improvement early on usually continue on a good path?  Sorry for all the questions.  This is all so new to me as I haven't been looking in this direction until recently.  I actually never thought the gluten free thing was going to make such a difference, but was desperate to feel better, and since doctor's haven't been able to figure it out, I decided it was time to take responsibility for my own body.

bartfull Rising Star

If you want further testing you need to be eating gluten. After a few weeks off of it you would need to go back on it - most folks say for three months. It's up to you. A lot of us are self-diagnosed. If you think it's important to have an official diagnosis, go for it. If you are staisfied that gluten-free makes you feel better, just stay gluten-free and forget about the doctor.

 

It is not unusual to have a few weeks of feeling great and then having a relapse. (It happened to me. I developed, or should I say uncovered, additional intolerances to both corn and soy.) But it sounds to me like you are getting CC'ed. You need your own dedicated condiments so no one contaminates them by double dipping. Your own toaster. You need to get rid of any scratched plastic or teflon. You need to avoid previously used wooden spoons and cutting boards and strainers. You need to make sure you don't wash your dishes with a gluten-y sponge. You need to use gluten-free lipstick and shampoo. Also, you should check any medications or supplements you take.

 

It sounds SO hard, but I promise, after a while it will become second nature. Read as many threads here as you can and feel free to ask as many questions as come to mind.

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Churley replied to Jane02's topic in Gluten-Free Foods, Products, Shopping & Medications
      10

      Desperately need a vitamin D supplement. I've reacted to most brands I've tried.

    2. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      48

      Supplements for those Diagnosed with Celiac Disease

    3. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      48

      Supplements for those Diagnosed with Celiac Disease

    4. - nanny marley replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      20

      Insomnia help

    5. - David Blake commented on Scott Adams's article in Product Labeling Regulations
      1

      FDA Moves to Improve Gluten Labeling—What It Means for People With Celiac Disease

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,346
    • Most Online (within 30 mins)
      7,748

    Scottweath
    Newest Member
    Scottweath
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Churley
      Have you tried Pure Encapsulations supplements? This is a brand my doctor recommends for me. I have no issues with this brand.
    • asaT
      plant sources of calcium, such as spinach, have calcium bound to oxalates, which is not good. best source of calcium is unfortunately dairy, do you tolerate dairy? fermented dairy like kefir is good and or a little hard cheese. i do eat dairy, i can only take so much dietary restriction and gluten is hard enough! but i guess some people do have bad reactions to it, so different for everyone.  
    • asaT
      i take b12, folate, b2, b6, glycine, Nac, zinc, vk2 mk4, magnesium, coq10, pqq, tmg, creatine, omega 3, molybdnem (sp) and just started vit d. quite a list i know.  I have high homocysteine (last checked it was 19, but is always high and i finally decided to do something about it) and very low vitamin d, 10. have been opposed to this supp in the past, but going to try it at 5k units a day. having a pth test on friday, which is suspect will be high. my homocysteine has come down to around 9 with 3 weeks of these supplements and expect it to go down further. i also started on estrogen/progesterone. I have osteoporosis too, so that is why the hormones.  anyway, i think all celiacs should have homocysteine checked and treated if needed (easy enough with b vit, tmg). homocysteine very bad thing to be high for a whole host of reasons. all the bad ones, heart attack , stroke, alzi, cancer..... one of the most annoying things about celiacs (and there are so many!) is the weight gain. i guess i stayed thin all those years being undiagnosed because i was under absorbing everything including calories. going gluten-free and the weight gain has been terrible, 30#, but i'm sure a lot more went into that (hip replacement - and years of hip pain leading to inactivity when i was previously very active, probably all related to celiacs, menopause) yada yada. i seemed to lose appetite control, like there was low glp, or leptin or whatever all those hormones are that tell you that you are full and to stop eating. my appetite is immense and i'm never full. i guess decades or more ( i think i have had celiacs since at least my teens - was hospitalized for abdominal pain and diarrhea for which spastic colon was eventually diagnosed and had many episodes of diarrhea/abdominal pain through my 20's. but that symptom seemed to go away and i related it to dairy much more so than gluten. Also my growth was stunted, i'm the only shorty in my family. anyway, decades of malabsorption and maldigestion led to constant hunger, at least thats my theory. then when i started absorbing normally, wham!! FAT!!!    
    • nanny marley
      Great advise there I agree with the aniexty part, and the aura migraine has I suffer both, I've also read some great books that have helped I'm going too look the one you mentioned up too thankyou for that, I find a camomile tea just a small one and a gentle wind down before bed has helped me too, I suffer from restless leg syndrome and nerve pain hence I don't always sleep well at the best of times , racing mind catches up I have decorated my whole house in one night in my mind before 🤣 diet changes mindset really help , although I have to say it never just disappears, I find once I came to terms with who I am I managed a lot better  , a misconception is for many to change , that means to heal but that's not always the case , understanding and finding your coping mechanisms are vital tools , it's more productive to find that because there is no failure then no pressure to become something else , it's ok to be sad it's ok to not sleep , it's ok to worry , just try to see it has a journey not a task 🤗
    • nanny marley
      I agree there I've tryed this myself to prove I can't eat gluten or lactose and it sets me back for about a month till I have to go back to being very strict to settle again 
×
×
  • 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.