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

Do I Need To Be Diagnosed?


Cargo

Recommended Posts

Cargo Newbie

For many many years I've known that most of my issues fall in the celiac symptom category...but I've chosen to ignore that because I didn't want to deal with going gluten free.

 

I've contacted my doctor to see if they'll do a test for me...I don't plan on stopping eating gluten until after the diagnosis comes back.

 

But if they refuse to do the test (it's the VA healthcare system, they might) and I choose to go gluten free, is there any other reason to make sure they diagnose me?  Is there anything that needs to be monitored by a doctor after going gluten free or is that it?

 

Thanks!


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



Celiac.com Sponsor (A8-M):



karenwill2 Newbie

Not all gluten issues show up on tests and there are many pathologies that going gluten free is the best treatment. It is super easy to eat gluten-free if you stick with lean meats and veggies. I just don't understand the "difficulty" that people worry about. It is so easy to read the ingredients and eat less processed foods. I have terrible insurance but all symptoms pointed to it, including the rash so my Doc did not run the test as the change in my diet was free. My insurance would not cover it plus I was maxed out already. I am so much better now and I eat out a lot. Today was the first time in 2 yrs that cross contamination got me. Felling better is so worth it.

GottaSki Mentor

Welcome Cargo!!!

 

I'd take a list of symptoms published by the University of Chicago along with a list of complete celiac antibody tests/nutrient blood tests.  

 

If your receive any push back - perhaps point out that celiac disease is managed by the complete removal of gluten -- when compared with other medical protocols -- it is inexpensive for the VA or any other health system to manage.

 

Push for the diagnosis....if you have had trouble wrapping your brain around living gluten-free in the past -- the diagnose will help if pesky doubt should sneak back in.

 

Open Original Shared Link

 

Full Celiac Blood Panel: 

Total Serum IgA
Tissue Transglutaminase IgA and IgG
Endomysial Antibody IgA
Deamidated Gliadin Peptide IgA and IgG

Gliadin IgA and IgG (only optional as the DGP above is the newer and more sensitive Gliadin test)

Also, low vitamins/minerals can indicate you are not absorbing nutrients properly - another indicator of Celiac Disease. So you might want to have these drawn at the same time as the Celiac panel.

Misc blood tests:
Bs, D, K, Iron, Ferritin, Copper and Zinc

 

Complete Metabolic Panel (CMP)

Complete Blood Panel (CBC)

tarnalberry Community Regular

I don't think that "the world" is in agreement on monitoring celiacs when a gluten free diet is adhered to.  Some docs want to monitor antibody levels somewhat regularly, and/or vitamin levels, and/or a few other things.  Some docs will take the knowledge of one autoimmune condition into account when working with other issues that come up.  Some docs don't want to do much of anything.  In my (completely layperson) opinion, a lot of it depends on your general health.  If you're *otherwise* fairly healthy, and if you're *otherwise* totally happy staying gluten free and you feel healthy that way, I simply can't fathom the need for lots of followup testing/monitoring.  If you're not, however, it could make a difference.

 

There's no clear cut answer, but I would suggest that just because a doctor doesn't want to test you for something, that doesn't mean you should keep making yourself sick by eating gluten if you know it bothers you.  Testing be whatever, your health is ultimately in your own hands.

GFinDC Veteran

Dr Peter Green's book says some high percentage of untreated celiacs have bone loss or the beginins of it.  I think it was something like 60% or more.  Anyhow, a bone density test might be a good idea..

Deaminated Marcus Apprentice

The reason I think testing is important is that Celiac can cause a myriad of health problems from osteoporosis, anemia, joint aches and other food intolerances and are associated with other auto immune disorders including Type 1 diabetis.

 

So if you later develop an auto immune disorder, having a Celiac diagnosis would help your doctor understand you condition better.

 

The only thing I didn't like when I was gluten free is that I couldn't go eat at a Burger place with friends and no longer being invited to diners.

 

As for eating: you can eat potatoes and rice and vegetables and cook your own meats.

There is gluten and wheat added to lots of prepared foods like soups, hot dogs, even corn bread.

You might need to try dairy free to see if that helps with gastrointestinal issues.

Let us know what the VA says.

 

PS:

don't just do the tTG test. Many test negative to it.

Here is the panel my local lab does:

 

Total IgA
Transglutaminase IgA tTG-IgA
Deaminated Gliadin IgA DGP-IgA
Deaminated Gliadin IgG DGP-IgG

 

It might be worth paying for it the one time to figure out once and for all if you have Celiac.

Cargo Newbie

I'm finally to a point in my life where I have the mental clarity to handle going gluten free.  I suffer from severe depression and anxiety and have just been consistently stable for the last year or so.  I've always suffered from IBS/loose stool, hormonal imbalances, acne, headaches, reflux, low ferritin, low D, and low potassium...not sure if they have ever really tested any other vitamins and minerals.

 

I'm always tired and have very little energy.  I take heavy B vitamins and Iron because without them, I'm almost non-fuctional.  My family diet is heavy on pasta and bread...and we eat out quite often, although we're cutting back...which is one reason I wouldn't consider going gluten free previously. 

 

If my doctors refuse to test me, or if the tests come back negative, I'll still go gluten free and see how things change.  I'd just prefer to have everything documented, of course. 

 

Thank you for all the information! 


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



Celiac.com Sponsor (A8-M):



GottaSki Mentor

I'm finally to a point in my life where I have the mental clarity to handle going gluten free.  I suffer from severe depression and anxiety and have just been consistently stable for the last year or so.  I've always suffered from IBS/loose stool, hormonal imbalances, acne, headaches, reflux, low ferritin, low D, and low potassium...not sure if they have ever really tested any other vitamins and minerals.

 

I'm always tired and have very little energy.  I take heavy B vitamins and Iron because without them, I'm almost non-fuctional.  My family diet is heavy on pasta and bread...and we eat out quite often, although we're cutting back...which is one reason I wouldn't consider going gluten free previously. 

 

If my doctors refuse to test me, or if the tests come back negative, I'll still go gluten free and see how things change.  I'd just prefer to have everything documented, of course. 

 

Thank you for all the information! 

 

 

Good Plan...and great luck to you!

 

Make sure you read the Newbie 101 Thread -- it contains a wealth of jump-start info.

nvsmom Community Regular

Good luck!  :)

 

When you do eventually go gluten-free, remember that the first few weeks can be really tough, especially if you go through a withdrawal.  Just remember it doesn't last.

Cargo Newbie

This is the response I got from my doctor:  


"Would recommend she cut out gluten for 2 weeks, then re-introduce it and if her 
symptoms return then she should stay on a gluten free diet. My experience is that 
not many people have true celiac's disease but a lot of people are sensitive or 
intolerent of gluten and should be on a gluten free diet."

Should I push to be tested??  What would your response be?  Is 2 weeks long enough for the small intestine to heal and have the effects disappear?  I'm annoyed.  I don't understand why she won't just test me.  It's not like it comes out of her pocket or she'd even have to do anything other than put the blood tests in the system.

GottaSki Mentor

Ugh!!!

 

That response is sooooo frustrating and silly really -- why not run the tests to be sure before gluten is removed before one loses the ability for tests to be accurate?  I would ask why she is not running these simple tests -- I'd push.

 

And no...most do not completely heal or lose all symptoms within the first two weeks gluten-free -- some improve right away, but two weeks is very fast to expect all symptoms to disappear.  The immune system is complex and can take some time before healing happens.

nvsmom Community Regular

Your doctor hasn't heard of withdrawal.   :rolleyes:  Often people feel worse for the first few weeks, not always but enough for it to be common. And not all symptoms resolve in the first few weeks. GI issues often heal first.Eventually that is often followed by migraines will improve and hair loss will slow. Neurological problems and pain are some of the last to go.... This is a generalization and not true of all celiacs, but my point is, that two weeks isn't much time to feel better, and it is most likely not even enough time to stop producing auto-antibodies never mind heal! The problem there is that if you do get tested after being gluten-free for any length of time, and you've stopped making auto-antibodies, your celiac tests will eventually be negative.

 

I would try to push for testing now and then try gluten-free after the tests. Your doctor is right that non-celiac gluten intolerance (NCGI) is much more common than celiac disease, but you might as well get tested for the rarer disease since you have symptoms, and you are eating gluten so the test will most likely be accurate.  

 

Good luck!

Cargo Newbie

Thanks for the info!  I had already sent my doctor another note...telling her that I'd really like to be tested, listing the tests I wanted and all my symptoms...

 

Then I was reading another thread and saw that medications may have gluten.  I'm on A LOT of meds...so it's not as easy as skipping the diagnosis and going on a gluten free diet!  I'd have to check all my medications...a good reason to make sure I get tested! 

GottaSki Mentor

Thanks for the info!  I had already sent my doctor another note...telling her that I'd really like to be tested, listing the tests I wanted and all my symptoms...

 

Then I was reading another thread and saw that medications may have gluten.  I'm on A LOT of meds...so it's not as easy as skipping the diagnosis and going on a gluten free diet!  I'd have to check all my medications...a good reason to make sure I get tested! 

 

yep...be careful with the med one -- all of us...me, son and daughter have been burned by that one more than once when pharmacy switches generics -- thankfully I am off all meds (except for benedryl, inhalers and epi pen as needed), son down to one -- unfortuanately daughter still has a basket full and is quite ill so tough to check every flipping time they are filled -- she is doing a bit better so hopefully she'll get off meds one day too.

Cargo Newbie

Looks like my doc went on vacation.  I won't hear back until mid to late next week. 

Cargo Newbie

Decided, just for the hell of it, to add on the thyroid tests to my request.  My symptoms all fall under Hashimoto symptoms as well, and thyroid issues run in my family.  I just want to feel better!  Being this tired and having all these issues can't be just...nothing.  I mean, I keep telling myself that maybe if I just lose weight, everything will be good again...but how can I work out when I'm so freaking exhausted? 

 

My doc will probably give me a lecture....ugh...stupid VA.  If I didn't have to get my care there, things would be so much easier.  My ability to advocate for myself is so limited. 

GottaSki Mentor

Ummm.....the difficulty you are facing is well know by many of us...HMO, PPO, VA, NHS, hmmm can't remember if Canada has abbreviations....the key is to understand the issues you want tested -- which it sounds like you do.  

 

Hang in there :) ...keep pushing :ph34r:  ...you will find answers  :blink: ...and I am sorry it is frustrating :unsure:  -- I completely understand the frustration  :huh:

Cargo Newbie

Doc ordered my celiac blood tests today!  I think I'm going to do a massive gluten challenge for two weeks before I get the tests done.  I found this article that said two weeks is enough. 

 

Open Original Shared Link

 

 

Instead of eating bread, I plan on buying a bag of gluten for baking and just mixing it will water and chugging it.  I figure two or three tablespoons a day will do it, if I am celiac!

nvsmom Community Regular

Good luck!  Enjoy an Oreo or beer for me.  :D

 

You might want to gluten yourself in the evenings so your days aren't negatively affected by feelings of poor health.

cavernio Enthusiast

Are you crazy??  Enjoy the forbidden foods while you can!

Speaking bags of gluten, the week before my dx I had scoured the store for one because I wanted to try making some vegan dishes with it. What a waste of my money!

 

Also, my personal experience is that I hardly felt better being gluten-free after 2 weeks. It's reaching a year now and I still suffer. If I did not get tested for celiac disease, and it didn't turn up positive, I would likely have ditched my diet ages ago. But I also wasn't as aware as you are of celiac disease, or of non-celiac gluten intolerance.

GFinDC Veteran

Doc ordered my celiac blood tests today!  I think I'm going to do a massive gluten challenge for two weeks before I get the tests done.  I found this article that said two weeks is enough. 

 

Open Original Shared Link

 

 

Instead of eating bread, I plan on buying a bag of gluten for baking and just mixing it will water and chugging it.  I figure two or three tablespoons a day will do it, if I am celiac!

 

Hi Cargo,

 

Two weeks may be enough for 75 percent of celiacs, but if you aren't part of that 75 percent, not so helpful.  Just remember if you get a negative result if t could just mean you are part of the other 25 percent who need longer gluten challenges.  I agree it's pretty good chance of a positive, but not so reliable as a negative.  Just something to be aware of.

Cargo Newbie

I haven't gone gluten free at all yet, but I realized that I've only  been eating a fairly small amount of bread recently and don't want to take any chances on a negative blood test. lol  I'm sure there's gluten in other things I've been eating, but I'm paranoid that it's not enough for the tests.  I know it's not logical. lol  I just want to over do it so I can be sure.

WendyRB Newbie

My doctor, who is a specialist in Celiacs Disease, said to eat at least two peices of bread every day for six weeks before being tested. You might want to watch chugging a whole bunch of gluten- if you are gluten sensitive or have Celiacs it might make you feel really horrible. And I agree with everyone else who says a two week challenge is basically worthless- I was put on a very strict elimination diet and didn't get to add gluten in for at least three months to make sure it was completely out of my system. When i went off of gluten I had a massive headache for five days. Since I went on the elimination diet for digestive issues, it took me a while to realize that my headaches had stopped when I went off of gluten. On this particular diet, when you add in a new food you eat it for three days, then do something else the next three days- they call it a Rotation Diet. It took me a while to realize that during my three days on gluten, I would get really irritable, yell at the kids, fight with my husband, and then get a headache.

Sometimes the symptoms are kind of subtle and you have to pay attention to get the cause and effect.

Cargo Newbie

I got my blood test done Monday...I didn't stuff myself with gluten before hand.  I wasn't eating a ton of it, but I certainly hadn't intentionally removed it from my diet so I'm sure if there's something to show, it'll show.

 

I also requested to be tested for Hashimotos so we'll see how that goes.

 

I have no idea how long it will take to get the results.  I'm nervous!

GottaSki Mentor

No need to stuff yourself with gluten....glad you got them done.  Most blood tests take less than 72 hours....yet results can take a week or so to hit your file.  Make sure you request written or electronic copies from your primary.

 

Hang in there :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,857
    • Most Online (within 30 mins)
      7,748

    LowellFrancis
    Newest Member
    LowellFrancis
    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

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • 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    
×
×
  • 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.