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

Would You Get Tested?


gfprof

Recommended Posts

gfprof Newbie

I've never put much faith in doctors, but after increasing GI distress over about a year and a half, I went to my doctor and complained that I thought I had a 'wheat allergy' (I didn't understand the difference at that point). She didn't do any testing, and instead gave me the 'eat more fiber' diagnosis along with the weird 'you get backed up and then it all comes out' explanation. (Hello: I'm having the opposite problem! Where do they get this stuff?) So I went wheat-free, then I was sick only when I ate out, then went gluten free for the last month, and I'm only sick when there's an accident (hidden ingredients, cross-contamination, etc.) This seems like a no-brainer to me, but friends and fam are pushing me to get tested. From lurking on this board, I understand that I have to eat wheat, get really sick, and be toilet- and bed-ridden for many days in order to do this.

Should I do it? Is it even worth it at this point? Has anyone ever had a 'verbal' diagnosis from a very understanding doctor? Am I ignoring another horrible possible disase?

Or should I just LIE to all of those well-meaning folks and say I've been diagnosed so that they'll leave me alone? :unsure:


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



Celiac.com Sponsor (A8-M):



Chicklet Rookie

I wouldn't and didn't. I too went on the gluten-free diet before any testing was done. I will not go back to eating gluten ever, I react strongly to accidents and that is enough proof for me. Not to mention when first going on gluten-free I felt better in 3 days. :D

Now you could find a doctor who knows about Celiac and Gluten Intolerance and he/she might just diagnose you from the diet reactions. :)

par18 Apprentice

Unfortunately I still believe the majority of the doctors out there don't understand the cause/effect of gluten intolerance enough to make a diagnosis based on diet response. That said I for one would like to have known that a diet change was a possibility for my years of symptoms. Even if I might not have gone or stayed on the diet at least I would have known the doctor was thinking it (Celiac) was a possibility. The only way I think real progress will be made as far as early diagnosis and treatment is if more people like yourself prove through diet response that your problem is related to something yhou are eating. I for one applaud anyone who has the knowledge and willpower to give the diet a chance and if successful be satisfied with the results and get on with their life. Whether you spend a lot of money on testing or "figure" it out for yourself the treatment is still the same. Good luck.

Tom

ravenwoodglass Mentor

Here is one possible way you may get your regular doctor to 'diagnose', if you have been ill and have been making frequent visits to your doctor and then he doesn't see you for a year or so and you walk in a different energetic person who has no complaints and then you tell him the only change was the gluten-free diet he may very well at least put gluten intolerant in your record. Doctors are becoming more aware of the drawbacks to the conventional testing, they can firmly rule celiac in but not out. The dietary response is the most important factor and you have that.

You might also consider being tested by Enterolab, they do fecal antibody testing and can also do genetic testing for the celiac genes. You doctor might diagnose based on the results of those tests and dietary response.

gfprof Newbie

Thanks everyone!

I feel so wonderful right now that I can't even imagine having to go through that. I think I'll take your advice about telling my doctor and maybe save a few people after me from the 'metamucil' prescription. ugh.

I will check out Enterolab too, so I can blame the parents later!

Ursa Major Collaborator

Good for you for staying on the diet. You know gluten makes you ill, and it is nobody's business what you eat or don't eat.

I was never officially diagnosed, but know that gluten is terrible for me. I am a very blunt person, beating around the bush is foreign to me. So, I tell people straight out that I can't eat anything containing gluten, and will not eat anything questionable.

I have no qualms when it comes to asking relatives to let me look at the ingredients of whatever spices, sauces etc. they have put into their cooking. If it is not safe, I won't eat whatever the questionable food is. I couldn't care less who might be offended. I refuse to be made sick by anybody's cooking.

Why do your friends and family want you to get tested? Who's body is it? Tell them that you are finally well, after being quite sick for a long time. You have no intentions of getting sick again only to confirm what you already know, namely that gluten makes you ill.

Your doctor had her chance of figuring it out and blew it. Why do people think that you have to be diagnosed by one of those doctors to justify being on the gluten-free diet? I think common sense is better than most doctors, especially when it comes to intolerances and diet. Doctors know precious little about nutrition and intolerances because very little time is spent on those subjects in medical schools.

The pharmaceutical companies control the medical schools, and they don't want people to be diagnosed with illnesses that don't require medication.

lucy lou Newbie
Unfortunately I still believe the majority of the doctors out there don't understand the cause/effect of gluten intolerance enough to make a diagnosis based on diet response. That said I for one would like to have known that a diet change was a possibility for my years of symptoms. Even if I might not have gone or stayed on the diet at least I would have known the doctor was thinking it (Celiac) was a possibility. The only way I think real progress will be made as far as early diagnosis and treatment is if more people like yourself prove through diet response that your problem is related to something yhou are eating. I for one applaud anyone who has the knowledge and willpower to give the diet a chance and if successful be satisfied with the results and get on with their life. Whether you spend a lot of money on testing or "figure" it out for yourself the treatment is still the same. Good luck.

Tom

Very well said, Tom. I'm beginning to feel much the same way as you-that if you feel better eliminating gluten it makes sense to just pay attention to how your body responds. I am very weary of the unending search for a doctor that "gets it". Wish I could pin point what hidden food additives-especially at restaurants cause reactions. Any thoughts?


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



Celiac.com Sponsor (A8-M):



ksymonds84 Enthusiast

Hello and welcome to the board! If you decide to stay gluten free without testing, read over the mayo clinic's website on celiac. They state that a diagnosis can be made through a positive dietary response. They also say not to do this if you want further testing because it will be negative. I feel that the Mayo Clinic in Rochester MN is one of the top notch facilities in the US and if they will diagnose on dietary response alone then thats all I need to know. I do have a understanding doctor that diagnosed me after being impressed that all my gastro symptoms went away on a gluten free diet (except when I accidentally mess up which happens alot in the beginning!) but those docs are extremely hard to find. Your family will hopefully come around when they see how much better you are but you have all of us here on the board for support whenever you need us!

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. - catnapt posted a topic in Related Issues & Disorders
      0

      anyone here diagnosed with a PARAthyroid disorder? (NOT the thyroid) the calcium controlling glands

    2. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      how much gluten do I need to eat before blood tests?

    3. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      Curious question

    4. - Amy Barnett posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Question

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

    • Total Members
      133,322
    • Most Online (within 30 mins)
      7,748

    avery144
    Newest Member
    avery144
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • catnapt
      learned I had a high PTH level in 2022 suspected to be due to low vit D  got my vit D level up a bit but still have high PTH   I am 70 yrs old (today in fact) I am looking for someone who also has hyperparathyroidism that might be caused by malabsorption    
    • catnapt
      I am on day 13 of eating gluten  and have decided to have the celiac panel done tomorrow instead of Wed. (and instead of extending it a few more weeks) because I am SO incredibly sick. I have almost no appetite and am not able to consume the required daily intake of calcium to try to keep up with the loss of calcium from the high parathyroid hormone and/or the renal calcium leak.    I have spent the past 15 years working hard to improve my health. I lost 50lbs, got off handfuls of medications, lowered my cholesterol to enviable levels, and in spite of having end stage osteoarthritis in both knees, with a good diet and keeping active I have NO pain in those joints- til now.  Almost all of my joints hurt now I feel like someone has repeatedly punched me all over my torso- even my ribs hurt- I have nausea, gas, bloating, headache, mood swings, irritability, horrid flatulence (afraid to leave the house or be in any enclosed spaces with other people- the smell would knock them off their feet) I was so sure that I wanted a firm diagnosis but now- I'm asking myself is THIS worth it? esp over the past 2 yrs I have been feeling better and better the more I adjusted my diet to exclude highly refined grains and processed foods. I didn't purposely avoid gluten, but it just happened that not eating gluten has made me feel better.   I don't know what I would have to gain by getting a definitive diagnosis. I think possibly the only advantage to a DX would be that I could insist on gluten-free foods in settings where I am unable to have access to foods of my choice (hospital, rehab, nursing home)  and maybe having a medical reason to see a dietician?   please let me know if it's reasonable to just go back to the way I was eating.  Actually I do plan to buy certified gluten-free oats as that is the only grain I consume (and really like) so there will be some minor tweaks I hope and pray that I heal quickly from any possible damage that may have been done from 13 days of eating gluten.    
    • Jmartes71
      So I've been dealing with chasing the name celiac because of my body actively dealing with health issues related to celiac though not eating. Diagnosed in 1994 before foods eliminated from diet. After 25 years with former pcp I googled celiac specialist and she wasn't because of what ive been through. I wanted my results to be sent to my pcp but nothing was sent.I have email copies.I did one zoom call with np with team member from celiac specialist in Nov 2025 and she asked me why I wanted to know why I wanted the celiac diagnosis so bad, I sad I don't, its my life and I need revalidaion because its affecting me.KB stated well it shows you are.I asked then why am I going through all this.I was labeled unruly. Its been a celiac circus and medical has caused anxiety and depression no fault to my own other than being born with bad genetics. How is it legal for medical professionals to gaslight patients that are with an ailment coming for help to be downplayed? KB put in my records that she personally spent 120min with me and I think the zoom call was discussing celiac 80 min ONE ZOOM call.SHE is responsible for not explaining to my pcp about celiac disease am I right?
    • Amy Barnett
      What is the best liquid multivitamin for celiac disease?
    • Jmartes71
      I've noticed with my age and menopause my smell for bread gives me severe migraines and I know this.Its alarming that there are all these fabulous bakeries, sandwich places pizza places popping up in confined areas.Just the other day I suffered a migraine after I got done with my mri when a guy with a brown paper bag walk in front of me and I smelled that fresh dough bread with tuna, I got a migraine when we got home.I hate im that sensitive. Its alarming these places are popping up in airports as well.I just saw on the news that the airport ( can't remember which  one)was going to have a fabulous smelling bakery. Not for sensitive celiacs, this can alter their health during their travel which isn't safe. More awareness really NEEDS to be promoted, so much more than just a food consumption!FYI I did write to Stanislaus to let them know my thoughts on the medical field not knowing much about celiac and how it affects one.I also did message my gi the 3 specialist names that was given on previous post on questions on celiac. I pray its not on deaf door.
×
×
  • 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.