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! Have To Eat Gluten Again!


F.deSales

Recommended Posts

F.deSales Rookie

I have been gluten free for 7 weeks. Had my first normal bm in months today. Went to the doc today said I need to have another EGD/colon done . This time I have to eat gluten for two weeks staring tomorrow to make sure the test is accurate. :( I am trying to get the courage to do so. I can't do the regular blood test because I have complete Iga deficiency.

When I think of the pain and hours I will spend in the "powder room" I get really scared. I am getting very depressed too. I am just starting to feel a bit better and now it is back to a living nightmare. My hubby is going to make sure I do as I am told because last time didn't and the procedure was canceled.

So, I guess I am just asking for pep talks and prayers. I know that you all have probably have gone though this also and I would appreciate some "I lived to tell about it"

Should I eat low gluten stuff or a little or what? :huh:

Thanks. This group is a blessing.

A~


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



Celiac.com Sponsor (A8-M):



sfm Apprentice
I have been gluten free for 7 weeks. Had my first normal bm in months today. Went to the doc today said I need to have another EGD/colon done . This time I have to eat gluten for two weeks staring tomorrow to make sure the test is accurate. :( I am trying to get the courage to do so. I can't do the regular blood test because I have complete Iga deficiency.

When I think of the pain and hours I will spend in the "powder room" I get really scared. I am getting very depressed too. I am just starting to feel a bit better and now it is back to a living nightmare. My hubby is going to make sure I do as I am told because last time didn't and the procedure was canceled.

So, I guess I am just asking for pep talks and prayers. I know that you all have probably have gone though this also and I would appreciate some "I lived to tell about it"

Should I eat low gluten stuff or a little or what? :huh:

Thanks. This group is a blessing.

A~

It really depends on how much you feel you need a diagnosis. I've been gluten free for going on 10 months now, despite negative blood testing. Because I could tell from how much better I felt what the answer was, tests or not.

Your G.I. does know what he's talking about, though. Lots of doctors don't bother telling their patients (or don't know) that they have to be eating gluten for the tests to be accurate. Mine didn't before my blood tests, so they might have been positive if I had them earlier.

I'm seeing a new G.I. who wants to do a biopsy anyway - he thinks my doctor should have ordered one based on my symptoms. But I know I have a choice - eat gluten and be sick for a few weeks, or don't, and accept the fact that my diagnosis will probably be incorrect.

One other thing - you haven't been gluten free that long - which means the damage may still be present, whether you go back to eating gluten or not.

I know I'm not answering any questions for you, but those are my thoughts...

Good luck.

Sheryll

Ursa Major Collaborator

Unfortunately, your G.I. doesn't know what he is talking about after all. After being gluten-free for seven weeks, two weeks won't be nearly enough to get an accurate test. It is quite likely that you would get a false negative, and be told that you can't have celiac disease.

It would at this point take at least three to six months of eating a lot of gluten (at least four slices of bread a day) to even have a remote chance of an accurate biopsy. And even then there is no guarantee.

Really, you have no choice but cancel the biopsy that is to take place in two weeks, as it will be utterly useless.

You now have two choices: The first one is to once more destroy your villi, making yourself very ill in the process, possibly causing irreparable damage to your intestines and possibly other parts of your body to have a biopsy in a few months, which may still not be accurate. The second one is, to listen to your body and realize that you feel so much better without gluten, and obviously have a problem with it, that it would be foolish to start eating it again.

Also, you could be tested with Open Original Shared Link, which will give you an accurate test result up to a year after starting the gluten-free diet. It is expensive, but worth it if you get the answers you need.

No doctor in the world can order you to make yourself sick again just to get a diagnosis you don't need. You already have your answer.

amberleigh Contributor

Before I found out I had celiac disease, my doc prescribed Bentyl to help with the diarrhea (we thought it was just my IBS flaring up again after the birth of my son). That stuff acts like industrial strength Immodium and it really helped a lot. I don't know if your doc can prescribe it for you to help while you're back on gluten??? Just a thought. Hang in there!

Oh and I got some side effects on the Bentyl for about an hour...dry mouth and a little dizzy/shaky...but I'll take that over diarrhea anyday!!

JNBunnie1 Community Regular

I couldn't agree more with Ursa. There is no medical reason to get a Celiac diagnosis, YOU already know you feel better. Why bother? What exact purpose would this diagnosis serve, really?

kbtoyssni Contributor

I don't see any reason to waste another 2+ weeks of your life just for a doctor. It sounds like you're perfectly convinced it's gluten and don't need another medical diagnosis to make you stop eating it. You do not need a doctor's permission to stay gluten-free.

Archived

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

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

    • Total Members
      132,918
    • Most Online (within 30 mins)
      7,748

    Dizzyma
    Newest Member
    Dizzyma
    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

    • xxnonamexx
      very interesting thanks for the info  
    • Florence Lillian
      More cookie recipes ...thanks so much for the heads-up Scott.  One can never have too many.  Cheers, Florence.
    • Russ H
      Hi Charlie, You sound like you have been having a rough time of it. Coeliac disease can cause a multitude of skin, mouth and throat problems. Mouth ulcers and enamel defects are well known but other oral conditions are also more common in people with coeliac disease: burning tongue, inflamed and swollen tongue, difficulty swallowing, redness and crusting in the mouth corners, and dry mouth to name but some. The link below is for paediatric dentistry but it applies to adults too.  Have you had follow up for you coeliac disease to check that your anti-tTG2 antibodies levels have come down? Are you certain that you not being exposed to significant amounts of gluten? Are you taking a PPI for your Barrett's oesophagus? Signs of changes to the tongue can be caused by nutritional deficiencies, particularly iron, B12 and B9 (folate) deficiency. I would make sure to take a good quality multivitamin every day and make sure to take it with vitamin C containing food - orange juice, broccoli, cabbage etc.  Sebaceous hyperplasia is common in older men and I can't find a link to coeliac disease.   Russ.   Oral Manifestations in Pediatric Patients with Coeliac Disease – A Review Article
    • cristiana
      Hi @Charlie1946 You are very welcome.   I agree wholeheartedly with @knitty kitty:  "I wish doctors would check for nutritional deficiencies and gastrointestinal issues before prescribing antidepressants." I had a type of tingling/sometimes pain in my cheek about 2 years after my diagnosis.  I noticed it after standing in cold wind, affecting  me after the event - for example, the evening after standing outside, I would feel either tingling or stabbing pain in my cheek.   I found using a neck roll seemed to help, reducing caffeine, making sure I was well-hydrated, taking B12 and C vitamins and magnesium.  Then when the lockdowns came and I was using a facemask I realised that this pain was almost entirely eliminated by keeping the wind off my face.  I think looking back I was suffering from a type of nerve pain/damage.  At the time read that coeliacs can suffer from nerve damage caused by nutritional deficiencies and inflammation, and there was hope that as bodywide healing took place, following the adoption of a strict gluten free diet and addressing nutritional deficiencies, recovery was possible.   During this time, I used to spend a lot of time outdoors with my then young children, who would be playing in the park, and I'd be sheltering my face with an upturned coat collar, trying to stay our of the cold wind!  It was during this time a number of people with a condition called Trigeminal Neuralgia came up to me and introduced themselves, which looking back was nothing short of miraculous as I live in a pretty sparsely populated rural community and it is quite a rare condition.   I met a number of non-coeliacs who had suffered with this issue  and all bar one found relief in taking medication like amitriptyline which are type of tricyclic anti-depressant.   They were not depressed, here their doctors had prescribed the drugs as pain killers to address nerve pain, hence I mention here.  Nerve pain caused by shingles is often treated with this type of medication in the UK too, so it is definitely worth bearing in mind if standard pain killers like aspirin aren't working. PS  How to make a neck roll with a towel: https://www.painreliefwellness.com.au/2017/10/18/cervical-neck-roll/#:~:text=1.,Very simple. 
    • Scott Adams
      We just added a ton of new recipes here: https://www.celiac.com/celiac-disease/gluten-free-recipes/gluten-free-dessert-recipes-pastries-cakes-cookies-etc/gluten-free-cookie-recipes/
×
×
  • 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.