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

Is Endoscopy Necessary?


beth01

Recommended Posts

beth01 Enthusiast

I was recently diagnosed with Celiac and had my children tested as a precaution, my daughter was having some troubles with constipation,fainting, and upset bellies for a while.  Her blood test came up positive and our GP said to have her go gluten free.  There isn't a pediatric GI in the town that we live in, one has to come from Mayo in Rochester.  When they called to set up the appointment, they had said they were going to do an endoscopy.  My problem is, she has been gluten free now and I don't want her to get sick having to do the gluten challenge.  I explained that to the nurse and she said if she has been gluten free to keep her that way and we can discuss it when she has her appointment on the 18th.  Is the endoscopy really necessary?  She is 11. Has anyone else gone through something similar?


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



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

For an endoscopy, the gluten challenge is shorter, 2-4 weeks, so it might be doable. If there is no doubt that she has celiac disease, then it is most likely not needed.  Some like to get it done to look for other problems, and others like to do it so they have a starting point to comapre back to if things do not improve on the gluten-free diet.  Some have it done to get the official diagnosis so accomodations can be made at school - that's the onl way it will help anything as a general rule.

beth01 Enthusiast

For blood tests for celiac, both her and I have had just the tTG IgA and the IgA.  I had the endoscopy the same time as the blood tests, I was really sick.  My GP that had Lainey tested was the one that said for her to go gluten free.  Can they officially diagnose her based on my Celiac diagnosis and the fact that her tTg IgA was >100?  Is there also more blood tests we should be having for the celiac?  I know about the basic blood panel( cbc, metabolic panel, and the vitamins) but I have seen some people having other Celiac tests.

Once again I am probably asking questions that can only be answered on a person to person basis, but I see my GI tomorrow and I know she is going to draw labs to see how I have been doing and not sure if I need to be having more done.  It's probably too late with the Celiac test though since I have been gluten free ( mostly besides a few mishaps) for two months.

 

Thank you again for all your input, both here and my other posts.  It's great to have people that actually understand what you are going through

glutenfreeliac Collaborator

Normally, I'd say if you don't need an "official" diagnosis and you or your daughter are seeing great improvement on the gluten-free diet, then skip the pain of the endoscopy. In the case of your daughter, I strongly suggest keeping her gluten free and talking to the doctor about options. Having a celiac diagnosis in hand may be helpful when it comes to school and other accommodations in the future. The doctor may have a better handle on ways to achieve your goals without putting your daughter through the pain and suffering (and recovery period) of the gluten challenge.

nvsmom Community Regular

Some doctors like to make sure it is celiac when dealing with the tTG IgA because it has a small (about 5%) false negative rate BUT that occurs mainly in the weak positive tests, like if the upper normal limit was 4 and she scored a 5. 100 is a high result regardless of what upper normal limit was used.

There are many other blood tests you could do to celiac disease. It would be best to do them right away if she will not be doing a gluten challenge. These are the tests:

TTG IgA and tTG IgG

EMA IgA - very similar to the tTG tests best tends to be positive in more advance cases. It is 98-100% specific to celiac disease

DGP IgA and DGP IgG - great tests for detecting early celiac disease or celiac disease in kids, as well as checking dietary compliance

AGA IgA and AGA IgG - older and less reliable tests

The complimentary tests are for D, A, K, Fe, Ca, Mg, B12, Cu, zinc, ferritin - those are the most common deficiencies. It is a good idea to check thyroid function too (TSH, free T3 and free T4, TPO Ab are good tests). Diabetes and thyroiditis are the most common c-occurring autoimmune diseases that accompany celiac disease, so it is a good Idea to keep an eye open for those.

  • 3 weeks later...
beth01 Enthusiast

Went to the Ped's GI today and he isn't going to do an endoscopy.  He feels comfortable officially diagnosing her based on my diagnosis and her tTg IgA.  He did draw the DGP tests so we will wait for them.  Has her going back in six months to have her tTg IgA checked again.  He had her checked for some deficiencies and thyroid testing and liver enzymes also.  Thanks for all your input!

BlessedMommy Rising Star

Congrats on getting the diagnosis! So glad that she doesn't have to do a gluten challenge.

 

Best wishes for good and improving health on the diet! :)


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



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

:)  Best wishes with going gluten-free.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,855
    • Most Online (within 30 mins)
      7,748

    Tara M
    Newest Member
    Tara M
    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

    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
    • Francis M
      Thanks. Since the back and forth and promises of review and general stalling went on for more than six months, the credit company will no longer investigate. They have a cutoff of maybe six months.
×
×
  • 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.