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

Now What?


Guest Nukapai

Recommended Posts

Guest Nukapai

Ok, so ... the current situation is this:

I've had a number of seemingly unrelated health issues (all kinds of gastro-intestinal problems, chronic catarrh, mild asthma, lactose intolerance, anemia, severe migraines, hair loss, rashes, hormonal problems, weight gain and now recently extremely rapid weight LOSS ...) that seem to have built up over time from when I was a child.

Recently (about two months ago) everything just came to a head and I was signed off sick for two weeks with acute gastro-intestinal problems and severe pain.

Someone suggested I might have Celiac disease, but when my doctor ordered a blood test for it, it came back clear, so he didn't then order an endoscopy or any other tests related to this condition.

He started exploring other avenues and ordered blood test after blood test (I'm changing my name to Pin Cushion Queen!) - until last week, one of them came back abnormal. It was my liver profile result, which showed abnormal levels of Bilirubin in the blood. He said I could have a blockage in my liver, or a severe case of gall stones (I've been in a LOT of pain over the last few weeks).

We are waiting for the local hospital to send me an appointment for an ultrasound.

MEANWHILE, I had the York labs private IgG screening done. I got my results today. In the "foods to avoid/strong IgG reaction" category were ... wheat, gliadin (so oats should be okay still), cow's milk and sunflower seeds.

Huh.

They included a bunch of fact sheets about Celiac, but made sure to mention that their test was NOT a Celiac diagnosis - however, they suggested showing the results to your doctor just in case.

So I'm not quite sure to what length I should now go in avoiding the above substances. I have been very unwell for about 7 weeks or so (I think, somewhere around that mark) that I'd be willing to do pretty much anything to get better again. And if these things are making me sick, I would GLADLY start looking into the gluten-free (and, sadly, wheat-free) diet with a mind to take it on board properly.

Not sure what I should do because there is no official diagnosis and my doc didn't seem interested in that avenue at all ... :blink:


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



Celiac.com Sponsor (A8-M):



GEF Explorer

In the very least, I'd say you were gluten intolerant. I posted this on the York thread, but you might look into HLA testing if you'd like a definitive answer on whether your intolerance could lead to celiac. It's also important to know that for family history purposes.

If you're negative for celiac after it's all said and done and you want to feel better... then I'd say to try the diet. I'd opt for a diet change over taking a pill for symptoms anyday! If you're intolerant, you'll most likely feel a lot better gluten-free... and in my opinion should be the most important thing.

Gretchen

Guest Nukapai

Sorry for my ignorance, but what is HLA testing?

I'm going to try the gluten free diet anyway, but I'm wondering about official diagnosis - in order to get it done, I understand you still have to be eating gluten, right? Now that I know it makes me sick, I don't want to eat any at all. An official diagnosis would help for professional reasons and so that I could get free info and support from the UK Coeliac charity organisation. On the OTHER hand, if I don't have Celiac, I might be able to just severely restrict gluten, but not drop it out completely.

GEF Explorer

HLA is a gene typing test where they check for the genes DQ2 & DQ8 (researched to be the celiac gene). If you're intolerant and you carry this gene, there is a risk that you could develop celiac (if you haven't already) later in life. If it is negative, you will not develop it, even though you are gluten intolerant and obviously have symptoms.

Gretchen

Guest Nukapai

Ah, thank you very much! I doubt I would be able to get that test done on the National Health System, so it would be another case of saving up for it...

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. - cristiana replied to tiffanygosci's topic in Introduce Yourself / Share Stuff
      2

      Celiac support is hard to find

    2. - cristiana replied to Dizzyma's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      4

      Newly diagnosed mam to coeliac 11 year old

    3. - tiffanygosci replied to tiffanygosci's topic in Introduce Yourself / Share Stuff
      2

      Celiac support is hard to find

    4. - trents replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

    5. - mamaof7 posted a topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

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

    • Total Members
      132,958
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • cristiana
      Hi @tiffanygosci Well done for reaching out,  fantastic you have found this forum. It sounds like you are managing the diet well, it can be overwhelming at first, but it will get easier.     I wonder if you have seen the short film 'Glutened'? - someone shared it on this forum a few months ago and it reminded me of how isolating it can be, particularly at first, when you don't know anyone with celiac disease.  *see link for film below. I realise now how blessed I was that when I was diagnosed two friends were also diagnosed around the same time, as we shared a lot of tips and recipes at the start.   Since then the number of people I know diagnosed with coeliac disease has grown and grown, there seems to be a much greater awareness of it among healthcare professionals and the public, at least this side of the Atlantic (I'm British).  I think in time you may find this, too. That said, those two coeliac buddies were 'straightforward' cases who seemed to recover very quickly when on a gluten-free diet - I struggled for some time.  So I found that I spent much more time discussing things with this online coeliac family. If you have any more questions, we're here for you.  I hope your event on 15th goes well.  Sounds like a good start!  I like you am not keen on Facebook, but perhaps setting up an account short-term might help? * https://vimeo.com/486284734 Cristiana     
    • cristiana
      You are very welcome @Dizzyma. Gastroenterologists are now following this rule in the UK more and more with children, so I am not surprised your daughter is not having an endoscopy.   Switching to a gluten free diet should begin to help, but also, even if you have to have testing done privately, it would be very helpful for you to find out if your daughter has vitamin and mineral deficiencies, which is highly likely,    In the UK tests are generally offered on the NHS for B12 and ferritin, and sometimes vitamin D.  Shortages in these can really cause any anxiety or depression or ramp it up. If you do end up supplementing, make sure your GP is aware as levels do need to be monitored, for example,  too much ferritin can cause huge health issues. Re: anxiety, definitely speak to a GP or another health care professional about this if it is an issue. Hopefully the Coeliac Society of Ireland will also be able to help. Cristiana  
    • tiffanygosci
      EDIT: I did find a monthly Zoom meeting for Celiacs through the Celiac Disease Foundation, so I'll be able to talk with some other people on January 15. And I also found a Celiac Living podcast on Spotify made by a celiac. I feel a little bit better now and I am still hoping I will find some more personal connections in my area.
    • trents
      Welcome to the celiac.com community, @mamaof7! It means for the one celiac disease antibody test that was ordered, she tested negative. However, other tests should have been ordered, especially for someone so young who would have an immature immune system where there would be a high probability of being IGA deficient.  The one test that was ordered was an IGA-based antibody test. It is not the only IGA antibody test for celiac disease that can be run. The most common one ordered by physicians is the TTG-IGA. Whenever IGA antibody tests are ordered, a "total IGA" test should be included to check for IGA deficiency. In the case of IGA deficiency, all other IGA tests results will be inaccurate. There is another category of celiac disease antibody tests that can be used in the case of IGA deficiency. They are known as IGG tests. I will attach an article that gives an overview of celiac disease antibody tests. All this to say, I would not trust the results of the testing you have had done and I would not rule out your daughter having celiac disease. I would seek further testing at some point but it would require your daughter to have been eating normal amounts of gluten for weeks/months in order for the testing to be valid. It is also possible she does not have celiac disease (aka, "gluten intolerance") but that she has NCGS (Non Celiac Gluten Sensitivity, or just "gluten sensitivity" for short) which is more common. The difference is that celiac disease is an autoimmune disorder that damages the lining of the small bowel whereas NCGS does not autoimmune in nature and does not damage the lining of the small bowel, though the two conditions share many of the same symptoms. We have testing to diagnose celiac disease but there are no tests for NCGS. To arrive at a diagnosis of NCGS, celiac disease must first be ruled out. A gluten free diet is the solution to both maladies.   
    • mamaof7
      For reference, daughter is 18 mths old. Was having painful severe constipation with pale stool and blood also bloating (tight extended belly.) Liver and gallbladder are normal. Ultrasound was normal. Dr ordered celiac blood test. We took her off gluten after blood draw. She is sleeping better, no longer bloated and stools are still off color but not painful.    "GLIADIN (DEAMID) AB, IGA FLU Value  0.84 Reference Range: 0.00-4.99 No further celiac disease serology testing to be performed. INTERPRETIVE INFORMATION: Deamidated Gliadin Peptide (DGP) Ab, IgA A positive deamidated gliadin (DGP) IgA antibody result is associated with celiac disease but is not to be used as an initial screening test due to its low specificity and only occasional positivity in celiac disease patients who are negative for tissue transglutaminase (tTG) IgA antibody."   Anyone know what in the world this means. She isn't scheduled to see GI until late April. 
×
×
  • 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.