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

Anorexia


muffin2

Recommended Posts

muffin2 Newbie

Hello!! Just curious I have been recently dx with Celiacs and had anorexia for 7 years. I am just curious if I have been possibly miss dx and instead of having celiacs is it possible that my symptoms are a result of my past?? I have had blood work done and a small biopsy and the blood work came back positive but the biopsy was negative. My symptoms are still there even though I am gluten-free. Thanks for any help you can give!! :D


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



Celiac.com Sponsor (A8-M):



KaitiUSA Enthusiast

I would go by the bloodwork. Biopsies are good to have but I have heard that if there is not alot of damage yet it can be missed. (that was not a personal experience it was a friends) Symptoms can take a while to go away. I have been gluten-free since Jan of 04 and it took months for the symptoms to go away. Make sure you don't have gluten sneaking in even in the very small amounts because that again will prolong the symptoms. Anorexia can also come with Celiac. Alot of people have eating disorders with Celiac. Hope this helps some :D

MySuicidalTurtle Enthusiast

Blood tests can be unreliable, too.

kvogt Rookie

Bloods tests are more likely to give false negatives. That is, they say you don't have the disease, when actually, you do have it. I've not read any reports of false positives. The disease is underdiagnosed for this reason - not overdiagnosed.

muffin2 Newbie

Thanks for replying. I keep getting different information on the blood tests. I am even getting a allergy test next week. Do you think this will be helpful??

VLK Newbie

Your eating disorder may have caused/triggered your Celiac Disease. This is what happened to me. It's unusual, but may be the case. Worth asking your doctor about.

muffin2 Newbie

Really. It makes sense no one else in my family has celiacs. I figured that being anorexic would come back to haunt me in the future. Thanks for your input!!


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



Celiac.com Sponsor (A8-M):



burdee Enthusiast

I totally disagree that an eating disorder esp. anorexia can 'trigger' celiac disease, although many doctors will blame EDs for just about anything to scare their patients into abstaining from their ED habits. I have corresponded with MANY people struggling with 'disordered eating' habits (including starving, restrictive dieting, bingeing, purging and laxative abuse) and also moderate a website for women who have 'struggled with disordered eating and are now committed recovery'. I have observed that many people use disordered eating, esp. avoiding eating or purging to COPE with celiac disease symptoms(before or after diagnosis). I myself have avoided eating for long periods to avoid the cramping pains or other intestinal discomfort after meals before I realized what I ATE caused those pains. I also have thrown up after eating when I hurt sooo bad that I couldn't tolerate anything passing through my digestive system.

I know anorexics who both starve to avoid celiac disease pain and purge after meals to cope with celiac disease pain. Of course chronic deprivation of food can influence later eating binges. So I see a thin line between disordered eating behaviors and coping with undiagnosed celiac disease symptoms. On the other hand, there are many people who used ED habits to cope with life stresses unrelated to physical pain. Those people do NOT have genetic predispositions for celiac disease and don't develop celiac disease. I also have heard stories about doctors blaming ED habits for ulcerative colitis, lactose intolerance and celiac disease. Doctors don't know much about celiac disease, but they know even LESS about disordered eating habits. ;)

BURDEE

cynicaltomorrow Contributor
Thanks for replying. I keep getting different information on the blood tests. I am even getting a allergy test next week. Do you think this will be helpful??

Allergy tests are generally a waste of time. Very few people have true allergies to foods. Celiacs isn't an allergy at all, it's an intolerance.

MySuicidalTurtle Enthusiast

Allergy testing is not a waste of time. She could have a wheat allergy and not Celiacs.

Mballerina Explorer

Celiac caused leaky gut and that is the main cause of food intolerance and food allergy, so testing is a good idea. The Lame Advertisement test is the best because it uses your white blood cell count as a baseling and therefore can even pinpoint intolerance.

  • 9 months later...
Guest The Weasel

I was about to say the same thing VLK did. I never had celiac disease show up in any blood tests my entire life (and I get blood tests done every single time I go to the doctor for all kinds of things. Celiac Disease never showed up until after I had gone through a lengthy period of disordered eating which also caused all kinds of other problems. My doctor didn't know about my eating problem so he's not the one who put the idea into my head. However, on several other message boards and livejournals I have read other people with disordered eating having tested positive for celiac disease afterwards. I wouldn't totally blame it, but I wouldn't discredit it either so it is a possibility.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,795
    • Most Online (within 30 mins)
      7,748

    susaneschiff
    Newest Member
    susaneschiff
    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

    • Colleen H
      The previous post did not come through right. I wonder if tingling burning feet are part of it.. I'm not sure if it's the med reaction that people with gluten intolerance get or the food we ate  It's frustrating because a person who did not want to admit to himself I had this condition wanted me to eat this chicken sandwich and now I'm stuck with a variety of symptoms plus now I'm hungry on top of it..  I'm new to this so I forget that "one bite" of the wrong thing can hurt us.😔. Do we stop eating if someone exposed us to gluten ??  My stomach is rumbling but my joints hurt ...  It's weird because I can feel the anxiety coming on.  I get joint problems ,  I don't know if anyone ever got hot flashes?? I suppose if it affects people head to toes you can get that too.   It's weird...hard to decipher what is what.   Also how long do I have to deal with this attack??  Makes me feel like not getting up out of bed.  I get too many symptoms which  horrible.  Thank you for your response..  
    • Colleen H
      Hello  I was glutened by a person that knew it.  I'm having 
    • wellthatsfun
      as my last post stated, i was diagnosed via endoscopy on the 14th of june. i have been eating amazing home cooked meals, luckily, mainly cooked by my boyfriend who is extremely careful about contamination (and is an incredible cook at that). however, i find myself in a mental rut still. being 18, this is the time in my life where i should be exploring things, going out, having fun. yet every corner i turn i'm tortured by the amazing smell of something i can't have anymore. the wonderful sight of such yummy foods. it's near torture. if my boyfriend and his friend who lives with us buy something i can't have, they'll usually eat it outside of the house or the car or wherever we are - which is greatly appreciated - but even seeing a burger or chips or a sausage roll in their hands guts me almost beyond repair. i just wanna have it again too. i miss it. i feel left out and it makes me very sad all the time. it's not their fault. they are allowed to eat whatever they want to, whatever their intestines will allow. it just stings, bad. and i feel so ungrateful given i basically have a private chef who is doubly the love of my life. but it's just so hard. i know i'll adapt. i haven't given up hope.i just wanted to vent. thank you for reading
    • RDLiberty
      Thank you. I must have misinterpreted a study or something. Thank you for the clarification. Much appreciated. Almost three years into my celiac diagnosis and I'm still learning new things. 
    • RMJ
      I wasn’t clear, glucagon and gadolinium were intravenous. I drank about 5 cups of the prep during 45 minutes. I feel very tired now, probably partly because I was nervous, and partly because I had to fast for 6 hours beforehand and wasn’t very hungry when I got home.
×
×
  • 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.