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

Undiagnosed, Feeling Unwell, Not Sure What To Do Next!


hopeonthemove

Recommended Posts

hopeonthemove Newbie

Hi!

In the last 2 years or so I've come to realize that desserts (with gluten and esp those with gluten and lactose) and some foods (pasta, crackers, etc) have kind of intense reactions with my body, and I've tried to stay away from them.  I haven't been tested, I'm kind of afraid of the cost of it knowing that it's only partially accurate, but some of my symptoms are:

 

tiredness (serious food coma/crashed on the couch after "white foods" inc pasta, potato, pizza, too much sugar, etc)

increased depression

bloating in stomach and face

scalp psoraisis, thinning hair

stomach cramps/diarrhea (I find that I only get this once I have seriously overdone it on gluten, it seems like I can get away with small amounts without this happening)

unable to lose weight

all-over body aches

enamel damage (the last time I went to the dentist, I had 7 cavities!  I've only had 3 others in my life)

 

My friend has very strong symptoms of celiac, she vomits whenever she eats even the smallest amount, but my mostly mild symptoms kind of lure me into the thought that it's too expensive and hypochondriac-like to go get tested, or really change my lifestyle if it's not presenting super strong.

 

I know that the most sensible thing would be to just cut out all gluten.  

Really, I know.  

I often feel like if someone could just walk up to me and say: "You have celiac disease.  You're going to kill yourself if you don't clean up your eating.", I would be able to do it with much more conviction.  And I can play those head games with myself, saying, "Yeah, I probably have it", but honestly I feel like I'm riding on the coattails of people who've actually been diagnosed.  Even though I know it would change my mindset and help me commit, is it weird to tell other people I have celiac when I don't know for sure?

 

 

 


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



Celiac.com Sponsor (A8-M):



freeme808 Apprentice

I'm totally in the same boat as you!!! I feel your frustration.  :unsure: I did go out of my way and pay for stool testing, which came did come back positive as far as having a reaction to it. I also have two genes(one from each parent) that supposedly makes me so much more prone to having this reaction? It said that I don't have the gene specific to Celiac and that Celiac is unlikely do to that fact. BUT I've also heard contradicting stories about the gene thing. Im at this point, where I think I might go in and tell the doctor to just prove me wrong...if he thinks that I don't have it, then please go ahead and prove me wrong!(I remember a lady saying that to her doc, and well she did have it). Like I said, cause even if I don't have it, I know I have a severe reaction to gluten. I think my fuel to know whether or not is due to 1) I want to start trying for a baby within the next year, and need to know for the sake of my child 2) on a social level it would be easier for me to deal, heck even on a personal level. 

Im think I'm just trying to figure out within myself how important knowing or not is...I know it's going to a bit of a frustrating process to go in one more time, but I'm thinking, at least I'll hopefully, finally know? <_<

I'm just debating if I should....

w8in4dave Community Regular

I also know what your going thru!! I have alot of the classic symptoms , I went in for blood work and it came back negative , I decided it was up to me to know what is good for my body and what isn't. I know gluten is not good for me!! So I decided on my own "I am not going back for more test" I will take care of me!! I will let my Dr. know next time I go see him I have gone gluten free, because he should know. If I continue to feel bad and have all the same symptoms I had before then, I know it is not Celiac, I may just be sensitive, But thats ok !! I will take care of me!! 

freeme808 Apprentice

w8indave, YES! Me too! 

I think we should listen to ourselves. I was really torn today...but, after a reality check...I know I can't doubt myself cause others do. I know what's best for me. I think the more confident I am in that aspect, maybe I will get more respect from others. 

 

Good luck to you both!  :)

Brandiwine Contributor

I wanted to get the tests done because it is weird to say you have Celiac when you don't have a diagnoses and people don't take it seriously if you call it a sensitivity. I just can not make myself go back to eating gluten knowing what it does to me, if one meal would be enough to test I still wouldn't want to but probably would. I just can't suffer for weeks for a diagnoses. :-/

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. - Jmartes71 replied to chrish42's topic in Doctors
      7

      Doctors and Celiac.com

    2. - Wheatwacked replied to MauraBue's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Have Tru Joy Sweets Choco Chews been discontinued??

    3. - Theresa2407 replied to chrish42's topic in Doctors
      7

      Doctors and Celiac.com

    4. - Scott Adams replied to MauraBue's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Have Tru Joy Sweets Choco Chews been discontinued??

    5. - Scott Adams replied to chrish42's topic in Doctors
      7

      Doctors and Celiac.com

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

    • Total Members
      133,263
    • Most Online (within 30 mins)
      7,748

    Fruitypebbles
    Newest Member
    Fruitypebbles
    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

    • Jmartes71
      I appreciate you validating me because medical is an issue and it's not ok at all they they do this. Some days I just want to call the news media and just call out these doctors especially when they are supposed to be specialist Downplaying when gluten-free when they should know gluten-free is false negative. Now dealing with other issues and still crickets for disability because I show no signs of celiac BECAUSE IM GLUTENFREE! Actively dealing with sibo and skin issues.Depression is the key because thats all they know, im depressed because medical has caused it because of my celiac and related issues. I should have never ever been employed as a bus driver.After 3 years still healing and ZERO income desperately trying to get better but no careteam for celiac other than stay away frim wheat! Now im having care because my head is affected either ms or meningioma in go in tomorrow again for more scans.I know im slowly dying and im looking like a disability chaser
    • Wheatwacked
      M&M Peanuts. About the same calories and sugar while M&M Peanuts have fiber, potassium, iron and protein that Tootsie Rolls ("We are currently producing more than 50 million Tootsie Rolls each day.") don't. Click the links to compare nutritional values.  Both are made with sugar, not high fructose corn syrup.  I use them as a gluten free substitute for a peanut butter sandwich.  Try her on grass fed, pasture fed milk. While I get heartburn at night from commercial dairy milk, I do not from 'grassmilk'.     
    • Theresa2407
      I see it everyday on my feeds.  They go out and buy gluten-free processed products and wonder why they can't heal their guts.  I don't think they take it as a serious immune disease. They pick up things off the internet which is so far out in left field.  Some days I would just like to scream.  So much better when we had support groups and being able to teach them properly. I just had an EMA blood test because I haven't had one since my Doctor moved away.  Got test results today, doctor ordered a D3 vitamin test.  Now you know what  type of doctors we have.  Now I will have to pay for this test because she just tested my D3 end of December, and still have no idea about my EMA.    
    • Scott Adams
      Some of the Cocomels are gluten and dairy-free: https://cocomels.com/collections/shop-page
    • Scott Adams
      Thank you for the kind words! I keep thinking that things in the medical community are improving, but a shocking number of people still post here who have already discovered gluten is their issue, and their doctors ordered a blood test and/or endoscopy for celiac disease, yet never mentioned that the protocol for such screening requires them to be eating gluten daily for weeks beforehand. Many have already gone gluten-free during their pre-screening period, thus their test results end up false negative, leaving them confused and sometimes untreated. It is sad that so few doctors attended your workshops, but it doesn't surprise me. It seems like the protocols for any type of screening should just pop up on their computer screens whenever any type of medical test is ordered, not just for celiac disease--such basic technological solutions could actually educate those in the medical community over time.
×
×
  • 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.