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 Please!


lvpriest

Recommended Posts

lvpriest Apprentice

Hi all,

So, I've been reading the posts in this forum and others, and it's like FINALLY opening a door to just an incredible understanding of myself for the last ten years!! I want to ask a few questions of you all, of those who have been through diagnosis, mis-diagnosis, the ups, the downs, the pains.

By way of recent background, I was referred to a gastroenterologist about 1 month ago. He undertook an initial consultation, then sent me for 4 different blood tests - well, 4 viles of blood were taken, and I can only remember that one said 'antibodies' and one said 'celiac.' Then the next week was the second set of tests - an ultrasound, and a barium follow through.

I am seeing him in a week and a half to go through the results.

What do you think he was looking for? My symptoms are as follows:

- severe bloating

- pooing (sorry!) every time I wee, always floating poops and always so poorly formed (like large maltesers)

- episodes of insane diarrhea

- cramping, leaky gas feelings

- nausea

- rash in my hairline

- dry eyes and mouth

- depression - I have been on cipralex for the last couple of months

I have a history of 'anorexia' but I have never wanted to restrict just wanted to make my tummy feel ok, and not bubbling. I also suffer from poor concentration and a certain haze over my brain sometimes. I just don't know what o. My bloating after every meal excessive gas and bathroom runs are ruining my life.

Dairy sends my stomach insane straight away, so I always have soy cappuccinos (the only vaguely dairy orientated product I'm having in the last couple of weeks - avoiding cheese, and yoghurt). Anyway, in the last two weeks, on two separate occasions, a soya capu has caused me to literally have to run to the bathroom with incredible diarrhea. I'm constantly fatigued, irrespective of how much sleep I get, and I am underweight.

I guess what I'm asking for is your opinion! Part of me is so so scared is I'm going to go back to the specialist and he's going to tell me nothing's wrong - but I know there is!

Thanks everyone, these forums are an incredible support in my feelings of hopelessness!


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

Oh boy do I know the fear of going in to a doctor and hearing nothing is wrong. I lived it for far too many years. I am a sero-negative celiac. I couldn't tell you how many times I was tested for it but no doctor ever mentioned the high rate of false negatives or told me to try the diet.

You do sound like you are in the right place. Don't go gluten free yet as your doctor may want to do an endoscopy if your blood work is positive. After all your testing is done do give the diet a strict try for at least a couple of months. If you choose to have an endo you can start the diet the day the endo is done. There are times when the blood work is strongly positive where doctors will diagnose then without the endo but most want that last test, which also has a high rate of false negatives.

The same area that is damaged by celiac produces the enzymes that help us digest dairy and some are able to go back to dairy after we heal. It would be a good idea to at least limit soy at first as some of us do have an issue with that. For your gluten free trial go with as much whole unprocessed fresh or single ingredient frozen food as you can. There is much to learn about the gluten-free lifestyle and your in the right place to learn it.

Also once gluten free make sure your meds, all OTC and script are gluten-free. You may find your depression resolves on the diet, many do.

mushroom Proficient

You have to be willing to listen to what your body is telling you, in addition to what your doctor is telling you. Your doctor can only tell you what his tests show (well, some are willing to think outside the body, but most stay within the testing box). You know what you live with every day and you know something is seriously wrong. From what you say it is most likely gluten causing you all the problems. So follow the advice of Ravenwoodglass, and give the diet a good trial no matter what the tests show.

P.S. If dairy and soy seem to be a problem you should also eliminate those, at least at first. If your gut is damaged you will have trouble digesting lactose until it heals, and many of us have problems with soy also.

tictax707 Apprentice

I can second so many things that you mentioned in your email. I was sick of doctors telling me I was fine when I knew I wasn't. I also know what it is like to not want to eat because empty is the only way my tummy is calm. Caffeine can be hard on your digestive system in general, so that may help explain that cappuccino incident. You are clearly ingesting something that your body seriously doesn't like. Even if you don't have celiac you may be gluten intolerant. Sometimes when your digestive system gets all inflamed it doesn't matter what you put in it, it will get mad. (even if it's foods that don't "normally" give you issues). Hopefully you will get some clear answers soon after all the tests. If its not gluten then you will have to do an elimination diet to figure out what it is, and it may not be just one thing your body doesn't like (just to prepare you...). Keep us posted on what the Dr says. I will cross my fingers for you getting some answers. :)

lvpriest Apprentice

Oh thank you all so so so much for coming back to me so quickly!!!

So what should I do? Another week and a half-should I just carry on going with gluten in case the doc wants to other tests, or will the tests I've done be conclusive enough?

Xxx

Skylark Collaborator

Looks sort of like my story too, especially the depression. Doctors never even suspected celiac. If you don't get a diagnosis, you can try the diet on your own. It sounds like you'd eliminate gluten, dairy, and soy for starters.

mushroom Proficient

Oh thank you all so so so much for coming back to me so quickly!!!

So what should I do? Another week and a half-should I just carry on going with gluten in case the doc wants to other tests, or will the tests I've done be conclusive enough?

Xxx

In the event your bloodwork is positive your doctor may recommend an endoscopy with biopsy. If you can hang on eating gluten until then I would probably do it, having come this far, unless he can't get you in for another two or three months in which case the additional torture (and damage) is probably not worthwhile in my book.


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



Celiac.com Sponsor (A8-M):



sb2178 Enthusiast

I would call to see if the blood work is back and find out precisely which tests were ordered. If it is, communicate your misery and say you want to be put on their cancellation list or squeezed in earlier. (Got any lightheadedness? Dizziness? Additional weight loss?) After your follow-up, you can go gluten-free if there is no biopsy, but if there is a biopsy keep eating it.

The other thing to consider is whether you are financially and physically willing to do a biopsy (really pretty mild for an invasive procedure). If you are not, then go ahead and stop eating it unless a full panel was not run.

Full panel:

IgA AGA

IgG AGA

IgA TTG

IgA EMA

total IgA

(Sometimes the DGP is substituted for the AGA but the "brain fogginess" tends to be captured in the AGA, so far as the very limited research shows. If the DGP was used, you could also ask for the AGA which is a broader test that is less closely tied to intestinal damage.)

charles76 Newbie

Hi, yes I agree caffeine can be difficult on your system, but it also helps counteract the brain-fog to think clearly about food options. I don't drink soy milk because I have a reaction I think due to the sweeteners (rice syrup is malted with barley sometimes) or the flavor (I'm sensitive even to the grain alcohol in vanilla extracts). While I may be unusually sensitive, it might be worth trying soy milk brands with that use only soybeans and water. Btw, I'm also sensitive to coffee itself, and drink tea and green tea (which is much easier on the system, though too much caffeine or sleeplessness by itself causes me digestive upset.

Keep trying though. I have had many, many doctors tell me I didn't have celiacs, and even had to do a second barium because they botched the first one. (They are looking for obstructions and diverticuli). Anyway, that was before most people had even heard of gluten, besides for pizza dough, so chances are better now for them telling you what you already can tell. And don't take them too seriously if they don't. An elimination diet (or finding an honest, knowledgeable alternative medicine practitioner) is, in my opinion, the most straight-forward common sense approach.

I just posted on another thread about my experience with setting up an elimination diet, called Elimination diet - Help!. You can also find it through my posts on my profile. Basically, meat, rice and applesauce, until you get better, unless you are extra sensitive like me.

Best of Luck!

safefood Newbie

Oh thank you all so so so much for coming back to me so quickly!!!

So what should I do? Another week and a half-should I just carry on going with gluten in case the doc wants to other tests, or will the tests I've done be conclusive enough?

Xxx

Trouble is, if you go gluten free now they won't be able to confirm celiac disease. My blood tests were not conclusive, ended up with a colonoscopy and that found the problem. When I used to eat white bread, one slice would put me to sleep within minutes. Also, was very depressed, because the wheat made me feel very tired and without energy to do much which mimic depression. Was diagnosed a couple of years ago but before had seen many doctors but was often misdiagnosed, including bipolar, (or as one doctor put it, manic-depressive with severe mood swings) and am no longer like that. Also, because of the damage from the gluten, for one year - no dairy products i.e milk, sour cream cottage cheese ( scrambled eggs were o.k.), and had to eat pureed vegetables during that time. I drank chamomile tea and water and rice milk without malt or barley. You Have to Read EVERYTHING on the labels of any food you consume unless you buy everything fresh and cook it yourself. I am also allergic to all fruit and fruit juices so that too is out of my diet. But this past year, I can now eat soft cooked vegetables, rice and mashed potatoes or potatoes without the skin. It takes time to heal.

  • 6 years later...
charles76 Newbie

Just adding an update to some advice I gave above. Been several years now and still can't digest any starches, basically at all.

So I live off steamed (shell easier) hard-boiled eggs, homemade brown sugar syrup, spinach (vit A!, and folic acid energy), celery, turkey, tuna, avocado oil, sometimes strawberries. Vitamin C powder in water is great. Some brands of dark chocolate for caffeine and histamine. MSG (Awake seasoning) ironically does wake up my nervous system in the dark winters combined with caffeine or fish oil). Falim gum is great for oral health (and salivary enzymes?) despite the BHT and artichokes and clams or scallops seem to help with energy. Allergic to browned proteins, beef in general (sad) and chicken make my soft tissue swell.

I've been trying Pure Encapsulations or Thorne pancreatin seems to help, and trying to work in vitamins (to see if I'm deficient, and for the vit Bs), and starch enzymes - but I'm allergic to many of them.

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. - JoJo0611 posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      0

      Awaiting Biopsy results

    2. - cristiana replied to emzie's topic in Related Issues & Disorders
      1

      Stomach hurts with movement

    3. - emzie posted a topic in Related Issues & Disorders
      1

      Stomach hurts with movement

    4. - Flash1970 replied to Ginger38's topic in Related Issues & Disorders
      3

      Shingles - Could It Be Related to Gluten/ Celiac


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,455
    • Most Online (within 30 mins)
      7,748

    jscal6
    Newest Member
    jscal6
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):



  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • JoJo0611
      I have had my endoscopy this morning with biopsies. My consultant said that it looked like I did have coeliac disease from what he could see. I now have to wait 3 weeks for the biopsy results. Do I continue eating gluten till my follow appointment in three weeks.  
    • cristiana
      Hi @emzie and welcome to the forum. Perhaps could be residual inflammation and bloating that is causing sensitivity in that area.  I was diagnosed with coeliac disease in 2013 and I remember some years ago my sister telling me around that time that she had a lady in her church, also a coeliac, who  had real pain when she turned her torso in a certain direction whilst doing exercises, but otherwise was responding well to the gluten-free diet. As far as I know is still the picture of health. I often end up with pain in various parts of my gut if I eat too much rich food or certain types of fibre (for some reasons walnuts make my gut hurt, and rice cakes!) and and as a rule, the pain usually hangs around for a number of days, maybe up to a week.   When I bend over or turn, I can feel it.  I think this is actually due to my other diagnosis of IBS, for years I thought I had a rumbling appendix but I think it must have just been IBS.  Reading the experiences of other sufferers, it seems quite typical.  Sensitized gut, build up of gas - it stands to reason that the extra pressure of turning can increase the pain. When I am glutened I get a burning, gnawing pain in my stomach on and off for some days - it isn't constant, but it can take up a few hours of the day.  I believe this to be gastritis, but it seems to hurt irrespective of movement.   Anyway, you are doing the right thing to seek a professional opinion, though, so do let us know how you get on.   Meanwhile, might I suggest you drink peppermint tea, or try slices of fresh ginger in hot water? A lot of IBS sufferers say the former is very helpful in relieving cramps, etc, and the latter is very soothing on the stomach. Cristiana
    • emzie
      Hi! One of the usual symptoms I have with a gluten flare up has deviated a bit and I thought I'd search for advice/opinions here. Also to see if anyone goes through similar stuff. Monday all of a sudden I got really bad pain in my stomach (centre, right under the chest, where the duodenum would be located). I ended up having to throw up for 2 hours, my body was trying to get rid of something from all sides and it was just horrible. Since then I havent been nauseous anymore at all, but the pain has stayed and it always worsens the moment i start moving. The more I move the more it hurts, and when i rest longer it seems to dissapear (no movement). I've had this before, but years ago I think around when I first got diagnosed with coeliac, where each time I moved, my stomach would hurt, to the point where I went to the ER because doctors got freaked out. That only lasted 1 night though, and Now it's already wednesday, so 3 days since then, but the pain persists and remains leveled. it doesn't get crazy intense, but it's still uncomfortable to the point I cant really go out because Im afraid itll turn into a giant flare up again. I couldn't think of where I could possibly have been glutened at this bad of a level and why it hasn't passed yet. I went to the GP, and as long as I have no fever and the pain isnt insane then its fine which I havent had yet. Tomorrow im also seeing a gastroenterologist specialized in IBS and coeliac for the first time finally in years, but I thought I'd ask on here anyway because it still hasnt dissapeared. It also hurts when someone presses on it. Maybe it's just really inflamed/irritated. I'm just frustrated because I'm missing out on my uni lectures and I do a sports bachelor, so I can't get behind on stuff & next to that i'm also going to go to the beach with my boyfriend's family this weekend: ( 
    • Flash1970
      Hi. So sorry to hear about your shingles. There is a lidocaine cream that you can get at Walmart that will help numb the pain.  That's what I used for mine. It can't be put near your eyes or in your ears. I hope your doctor gave you valacyclovir which is an antiviral.  It does lessen the symptoms. If it is in your eyes,  see an ophthalmologist.  They have an antiviral eye drop that can be prescribed.  Shingles in the eye could cause blindness.  I was unsure whether you have celiac or not.  If you do,  follow the diet.  I believe that extra stress on your body does affect everything. Shingles can recur. If you start getting the warning signs of nerves tingling,  see the dr and start taking the valacyclovir to prevent a breakout. If I sound technical,  I am a retired pharmacist. 
    • Scott Adams
      You are right to be proactive, as research does indicate that individuals with celiac disease can have a higher predisposition to enamel defects, cavities, and periodontal issues, even with excellent oral hygiene. While many people with celiac successfully undergo orthodontic treatment without complication, your caution is valid. It may be beneficial to seek a consultation with an orthodontist who is familiar with managing patients with autoimmune conditions or who is willing to collaborate with your daughter's gastroenterologist or a periodontist. They can perform a thorough assessment of her current oral health, discuss your specific concerns about recession and decay, and create a tailored hygiene plan. This second opinion could provide a clearer risk-benefit analysis, helping you decide if addressing the cosmetic concern of the lower teeth is worth the potential risks for your daughter, especially if they are not currently affecting function or her confidence. 
×
×
  • 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.