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

Does Anyone Binge On A Celiac Attack?


Mballerina

Recommended Posts

Mballerina Explorer

I have found that everytime i eat gluten I begin to binge. My hunger is unquenched. I feel so hungry and nauseous and have a migraine. The only time nausea and the migraines go away it is because I am eating. This has become very horrible and I cannot function. I can predict the whole course of it and it always lasts from 2 to 4 days. I am having sort of an emotional breakdown because I really can't stop it and I can't make it end faster. I feel like a schizo basket case, one day okay and the next a complete desparate depressive.


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



Celiac.com Sponsor (A8-M):



mjbennett88 Newbie

Hi,

I'm new to this forum and have been reading for quite a while. Newly diagnosed a couple of months ago and I don't seem to have a typical progression. I'm sure the celiac was triggered last April when I was under a tremendous amount of stress with two deaths in my immediate family 1200 miles away from home. I can pinpoint when the symptoms started, but they weren't really anything that dramatic. Diagnosis came when I went in for a checkup and the dr noticed I was anemic and asked what else was going on. She had it nailed on the first try and referred me to a GI guy. Blood test was negative, but the endoscopy was positive.

Anyway, I've been good for a long time, but yesterday I just lost it. I had two social gatherings and just absolutely could not resist cheese and crackers and oatmeal chocolate chip cookies. I was also kind of curious to find out if I would have a reaction since I have not tested it since going gluten-free. The only negative reaction was hardly mentionable. I'm wondering if there are degrees of celiac disease and if this may indicate that I have maybe a "mild" case and may not have to be as careful as some people who have really bad reactions to any gluten at all. That could be wishful thinking and everything I have read would not indicate that it's true, but are some of us maybe more tolerant of gluten thatn others?

JUDI42MIL Apprentice

Mj- all I know is my mom has celiac, and she cheats, eats all kinds of things I could never. I seem to react right away now, if I mess up and get even the smallest amount.In fact I seem much worse now than before I went gluten-free.

darlindeb25 Collaborator
:( not all celiacs have violent reactions to gluten--i dont have a noticeable reaction to barley, but i know it is still in there causing damage :angry: --you have to all realize this--even if you dont have a reaction that you can notice--that doesnt mean that the gluten isnt doing just as much damage :ph34r: --we CANT cheat--craving something is natural, but you are the only one putting that food in your mouth--no one else makes you do it--celiacs is not making you eat, you are--always remember--you are your own worst enemy :o ----i am sure everyone else on this board has craved the things we cant have--i know i have---i want egg noodles with cream of chicken soup in the worst way, but i want to feel good so much more ;) --this is up to you--only you can keep you healthy--you must be strong---i know this may sound like a lecture, i guess it is--only you can take care of you--as long as you cheat, you are hurting yourself and the ones that love you--deb
clanning Rookie

Mballerina,

I have the same cravings and binges. I've tried baking gluten-free and have failed!! Therefore, I want what I can't have. The hardest thing is.... I want a beer once in awhile.

My husband can tell when I have had gluten. I get real crabby, angry, b%$@#y, etc.. It will last about a week. I also feel real run down and exhausted. I also get the worst stomache, doubling over, holding my breath!! I don't get violently sick like I did 10 yrs ago or even 2 yrs ago. I still function because I've done it to myself. No one forces us to eat gluten.

Eating gluten only makes me miserable and my family.

I can't tell you that we are wrong for our cravings. We are like little kids, telling somebody that they can't have something seems to only make them want it more. It's hard and all we can do is try.

clanning

jenni Newbie

I have been gluten-free for 3 years and I haven't cheated once. ( I accidentally ate a part of a flour tortilla when I was told they were corn, but that's it) I have disease "phobia" and the list of cancers and other autoimmune diseases that can be triggered by eating gluten are too long and horrifying for me to even think about cheating. There is nothing that tastes as good as being cancer free feels.

Rikki Tikki Explorer

I have had the same symptons as you describe usually before I get really sick. I have heard it referred to before as starving stomach, it is the most fierce starving sensation and usually followed by being very ill.

I don't think I have intentionally cheated in over a year because I have found that the price I pay for even a small amount of gluten is not worth the immediate gratification that I would get by eating the food I miss the most.

The hardest part I am having is that I have been unable to put all of the weight on that I initially lost. It seems like the food is so expensive and very hard to find in the small town I live in. Many people will say to order it on the internet but there again it is very expensive.

Lately I have been having instances where my heart will beat very fast and I am very tired. I would like to feel as happy and healthy as I did before I got so sick. It took probably at least 15 years from the time I forst noticied I was ill and couldn't relate it to food poisioning or the flu.

For many years the doctor said that I had irritable bowel and after that I was too embarrased to ask again and it wasn't until a dramatic weight loss that the doctor looked further, if I remember right it was 25 pounds is about a six week period. Several years before the actual confirmation a doctor had said my blood work showed a disease called celiac but that it was so rare that he was sure the blood test was wrong.

Finally the blood test was done again showing positive and I was sent to a GI doctor who did the biopsy that confirmed that it was celiac and the villi was gone.

There are not any support groups in the area where I live and I feel very alone in this.

I am 5'7" and weigh about 112 pounds and believe me it is not attractive, with the women I work with who are trying to lose weight they don't want to hear about or understand my dilema. Any suggestions would be very much appreciated.


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



Celiac.com Sponsor (A8-M):



tarnalberry Community Regular

Granger,

Well, at least having the correct diagnosis well help. You might want to stock up on nuts and avocados and any other high-caloric density foods you find to help put some weight back on. (You might want to consider weight training - while eating plenty of calories - to add muscle as well.) Sticking with naturally gluten-free foods will help keep the costs down and keep you from having to find speciality stores.

Rikki Tikki Explorer

Thank-you Tiffany for your information. I am really unclear on what is naturally gluten free. I know fruit and vegetables are but am so lost on what else is. It is just so confusing!

Sally

glen4cindy Apprentice

I will have to add too that I am striving to avoid gluten all I possibly can. I am still learning what I can and cannot have. Sure, I crave Krispy Kreme's, but, I KNOW I cannot have that.

The price that I pay for accidentally comsuming gluten is way worse than any amount of purposeful "fudging" would provide!

darlindeb25 Collaborator
;) my 2 cents worth again :rolleyes: ---i have never intentionally cheated after going gluten-free--i never even had the desire to cheat--i was so sick for so long and i tried to avoid what i thought was making me sick--i love vegetables and the only ones i could eat that didnt bother me were green beans and sometimes carrots--little did i know it wasnt the veggies causing the problem :angry:--i work in a convience store and we sell krispy kremes and they have not once tempted me--i was dyvastated when i realized i couldnt have nacho cheesier doritoes--i never could eat them before and now i can and cant have them :unsure: ---there are many good things we can still have--the one thing that would have done me in is peanut butter :( i would have a very hard time giving it up and i do crave egg noodles ;) --i cant find any noodles that compare, maybe my standards are too high--you can look at celiacs as a life sentence or you can look at it as having your life back--i prefer to be happy i feel so much better :D finding out about celiacs has given me back my life :D deb
lilliexx Contributor

i am gluten intolerant ( non- celiac) i had severe stomach problems on a daily basis for 5 years. I have stopped eating wheat gluten and my stomach is normal now :) i am not really effected by barley gluten so i still drink beer. I know i shouldnt, but since it doesnt give me problems that i can feel its a lot easier to justify having it. Beer is the only thing i havnt given up. i even sat at a pizza restaurant with my son last night and wasnt even tempted to have a piece. Its easy to not want to eat wheat, since i know what it does to my stomach.

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. - DebD5 commented on Scott Adams's article in Spring 2026 Issue
      1

      The Dark Side of Gluten-Free: Counterfeit Labels and Global Food Safety Failures

    2. - Jmartes71 replied to Jmartes71's topic in Doctors
      6

      Second chance

    3. - trents replied to EssexMum's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Concerning GP advice

    4. - knitty kitty replied to HectorConvector's topic in Related Issues & Disorders
      327

      Terrible Neurological Symptoms

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

    • Total Members
      133,641
    • Most Online (within 30 mins)
      7,748

    JennaK23222
    Newest Member
    JennaK23222
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • Jmartes71
      Thats the thing, diagnosed in 1994 before foods eliminated celiac by biopsy colonoscopy at Kaiser in Santa Clara  now condo's but it has to be somewhere in medical land.1999 got married, moved, changed doctor's was with former for 25 years told him I waz celiac and that.Fast forward to last year.i googled celiac specialist and what popped up was a former well known heard of hospital. I thought I would get answers to be put through unnecessary colonoscopy KNOWING im glutenfree and she wasn't listening to me for help rather than screening me for celiac! Im already diagnosed seeking medical help.I did all the appointments ask from her and when I wanted my records se t to my pcp, thats when the with holding my records when I repeatedly messaged, it was down played the seriousness and I was labeled unruly when I asked why am I going through all this when its the celiac name that IS what my issue and All my ailments surrounding it related. I am dea6eoth the autoimmune part though my blood work is supposedly fabulous. Im sibo positive,HLA-DQ2 positive, dealing with skin, eye and now ms.I was employed as a bus driver making good money, I loved it for the few years my body let me do until I was yet again fired.i went to seek medical help because my body isn't well just to be made a disability chaser. Im exhausted,glutenfree, no lawyer will help and disability is in limbo thanks to the lax on my health from the fabulous none celiac Google bay area dr snd team. Its not right.
    • trents
      Welcome to the celiac.com community @EssexMum! First, let me correct some misinformation you have been given. Except in the case of what is known as "refractory" celiac disease, which is very rare, it is not true that the "fingers" will not grow back once a consistently gluten free diet is adopted. Celiac disease is an autoimmune condition whereby the ingestion of gluten triggers an inflammatory process that damages the millions of tiny finger-like projections that make up the lining of the small bowel. We call this the "villous lining". Over time, continued ingestion of gluten on a regular basis results in the wearing down of these fingers which greatly reduces the surface area of this very important membrane. It is where essentially all the nutrition from what we eat is absorbed. So, losing this surface area results in inefficiency in nutrient absorption and often to medical problems related to nutrient deficiencies. Again, if a gluten-free diet is consistently observed, the villous lining of the small bowel should rebound. "We was informed that her body absorbs the gluten rather then rejecting it and that is why she doesn't react to the gluten straight away, it will be a build up and then the pains start. " That sounds like unscientific BS to me. But it does sound like your stepdaughter may have a type of celiac disease we know as "silent" celiac disease, meaning, she is asymptomatic or at least the symptoms are not intense enough to usually notice. She is not completely asymptomatic, however, because you stated was experiencing tummy aches off and on. Cristiana gives some good suggestions about ordering "safe" food for your stepdaughter from restaurant menus in Europe. You must realize that as the step parent who only has her part of the time you have no real control over how cooperative her other set of parents are with regard to your stepdaughter's needs to eat gluten free. It sounds like they don't really understand the seriousness of the matter. This is very common in family settings where other members are ignorant about celiac disease and the damage it can do to body systems. So, they don't take it seriously. The best you can do is make suggestions. Perhaps print out some info about celiac disease from the Internet to send them. Being inconsistent with the gluten free diet keeps the inflammation smoldering and delays or inhibits healing of the villous lining. 
    • Scott Adams
      Here are some articles on cross-reactivity and celiac disease:      
    • knitty kitty
      @HectorConvector, Here are some articles about "dry Beriberi" and neuropathy.  I hope you've been able to acquire thiamine hydrochloride or Benfotiamine.  I'm concerned.   Dry Beriberi Due to Thiamine Deficiency Associated with Peripheral Neuropathy and Wernicke's Encephalopathy Mimicking Guillain-Barré syndrome: A Case Report and Review of the Literature https://pubmed.ncbi.nlm.nih.gov/30862772/ Dry Beriberi Manifesting as Acute Inflammatory Demyelinating Polyneuropathy in a Patient With Decompensated Alcohol-Induced Cirrhosis https://pmc.ncbi.nlm.nih.gov/articles/PMC7707918/ A Rare Case of Thiamine Deficiency Leading to Dry Beriberi, Peripheral Neuropathy, and Torsades De Pointes https://pmc.ncbi.nlm.nih.gov/articles/PMC10723625/
    • cristiana
      Good evening @EssexMum You are quite right to be concerned about this situation.  Once diagnosed as coeliac, always a coeliac, and the way to heal  is through adopting and sticking to a strict gluten diet. That said... I have travelled twice to France since my diagnosis, firstly in May 2013 and again in August 2019.   My spoken French isn't bad, and whilst there I tried my best to explain my needs to chefs and catering staff, and I read labels very carefully when shopping in supermarkets, but both times I came away with worsening gastric symptoms and pain. Interestingly,  after the second holiday, my annual coeliac review took place the following month and although I'd been very careful to avoid gluten all year, thanks to that August holiday my coeliac antibodies were elevated,  Clearly I hadn't been imagining these symptoms and they must have been caused by gluten sneaking in somehow. When I spoke to my gastroenterologist on my return, who is an excellent doctor, he told me with a smile that this was a very common experience in France among his patients, and not to worry too much about it! In fact, before we went away in May 2013, which was just after I had been formally diagnosed, he told me not to even bother trying to adopt a gluten free diet until I returned, knowing what France was like, but I was feeling so awful at that time I ignored his advice and at least tried to make a start with it. (I ought to say - both these visits were some time ago, so perhaps things are a lot better there now.) So what to do?  I would say at least try to explain to catering staff the situation - they should be able to rustle up a plate of cheese, boiled eggs, tuna, salad and fruit, and if things like crackers and gluten-free pot noodle or oats can be packed in the UK, those can be produced at mealtimes.    Of course, most larger supermarkets in France do now cater for coeliacs, but when I was last there the the choice wasn't as wide a range as we have in the UK but I think that is partly because the French like to cook from scratch, whereas our gluten-free aisles have quite a lot of dried or pre-baked goods in them/convenience foods, because I think we as a nation tend to use them more. I would be worth doing a bit of research on the internet before the trip, - the words you want are 'sans gluten'.  I've just googled 'sans gluten Disney Paris" and this came up.  I do hope at least some of this is of help. https://www.tripadvisor.co.uk/Restaurants-g2079053-zfz10992-Disneyland_Paris_Ile_de_France.html  Whatever befalls in France, at least your stepdaughter can resume her usual diet on her return. On a related tack, would you be happy to post any positive findings/tips upon her return - it might be of use to others travelling to Disneyland Paris with children in future? 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.