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

What Are You Thoughts About This


twe0708

Recommended Posts

twe0708 Community Regular

So I was recentely dx with celiac disease and I asked my doctor how serious I need to take this and is it ok to have say a beer or a cupcake once a year. He said if I was at a party and didn't want to hurt the hostess' feelings while celebrating a big event then a beer or piece of cake would be ok. Is this true? :huh:


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



Celiac.com Sponsor (A8-M):



Lisa16 Collaborator

Sorry to tell you this twe, but your doctor is just flat out wrong.

The truth is that people with celiac disease need to be as gluten free. Everytime you eat some, you are seriously damaging your health. If you read more of the posts on this board, you will understand why this is so. To continue eating gluten will actually increase your odds of premature mortality (not to mention a host of other related ailments). Read a few articles on pubmed-- there is a recent study by the Mayo Clinic that supports this. Read the Peter Green book, "Celiac, the Hidden Epidemic." I am afraid that even if your symptoms are mild, this is still the case.

I am afraid there must be no more regular beer and no more regular cupcakes in your future. You will, however, find recipes for gluten-free cupcakes here. And there are such things as gluten free beers. So you will be just fine.

Now the truth is also that from time to time you will accidentally get glutened. Whenever this happens, you will experience a kind of set-back in your recovery. Once you are gluten free and experience what it is like to live free of pain and free of your symptoms, these setbacks will feel horrible and, depending on the severity, may last a few weeks. The longer you are gluten free, the worse the accidents will be for you. For most of us, this is incentive enough.

Good luck in yor transition to a gluten free lifestyle. I am afraid there will be awkward social moments and difficult situations. But that is why we are here. And remember... no matter how bad you think it is, somebody here will have experienced the same thing.

Also, you may consider looking for a doctor who is more knowledgeable about the disease.

Lisa

Shess0816 Apprentice
So I was recentely dx with celiac disease and I asked my doctor how serious I need to take this and is it ok to have say a beer or a cupcake once a year. He said if I was at a party and didn't want to hurt the hostess' feelings while celebrating a big event then a beer or piece of cake would be ok. Is this true? :huh:

That is really funny you mentioned this, because my doctor said that very same thing too! I personally have chosen not to follow that advice. I know how sick I get when I ingest something with gluten and it's just not worth it to me to be sick for 2 weeks for one beer or one cupcake. They may not taste as good, but they do make cupcakes and beer without gluten -- and I personally would much rather feel good the following two weeks!

Back to the doctor, though, he said that he believes there just has not been enough research done on gluten and celiacs to really know what the body can and cannot take. He believes that once you rid yourself of the influx of gluten from eating it for years, your body can tolerate a certain amount. He believes that it is all about finding what amount your body is okay with. Interesting concept, but like I said, I feel bad when I accidently ingest just a little gluten. I don't really want to take the time to figure out how much my body can handle... I actually don't really buy that whole thing at all, but I think he's just trying to help....

Shess0816 Apprentice
Sorry to tell you this twe, but your doctor is just flat out wrong.

The truth is that people with celiac disease need to be as gluten free. Everytime you eat some, you are seriously damaging your health. If you read more of the posts on this board, you will understand why this is so. To continue eating gluten will actually increase your odds of premature mortality (not to mention a host of other related ailments). Read a few articles on pubmed-- there is a recent study by the Mayo Clinic that supports this. Read the Peter Green book, "Celiac, the Hidden Epidemic." I am afraid that even if your symptoms are mild, this is still the case.

I am afraid there must be no more regular beer and no more regular cupcakes in your future. You will, however, find recipes for gluten-free cupcakes here. And there are such things as gluten free beers. So you will be just fine.

Now the truth is also that from time to time you will accidentally get glutened. Whenever this happens, you will experience a kind of set-back in your recovery. Once you are gluten free and experience what it is like to live free of pain and free of your symptoms, these setbacks will feel horrible and, depending on the severity, may last a few weeks. The longer you are gluten free, the worse the accidents will be for you. For most of us, this is incentive enough.

Good luck in yor transition to a gluten free lifestyle. I am afraid there will be awkward social moments and difficult situations. But that is why we are here. And remember... no matter how bad you think it is, somebody here will have experienced the same thing.

Also, you may consider looking for a doctor who is more knowledgeable about the disease.

Lisa

Just to build a bit on what Lisa said, too, at some point you have to not worry about whether you hurt someone else's feelings. When I first got diagnosed I was so worried about what everyone would think and whether I'd hurt my boyfriend's parents' feelings when they cooked dinner for us that I slipped up a few times just to be polite. After a couple times of that and several weeks of the aching joints, bathroom trips, headaches, fogginess, stomach pains, I decided that this is about my health. If people are going to feel bad because I want to be healthy and can't eat the cupcakes they made, it's their problem. I am not going to subject myself to a higher risk of cancer and infertility (among other potential issues!) just to make someone feel better about their cooking. Now, when I go to parties where people may not understand my disease, I take my own food or I eat before. Sometimes we call ahead if they are good friends and see exactly what they will be serving and how they are preparing it. For example, we went to a rehearsal dinner for a good friend's wedding and they just had a little cookout with burgers and brats. Well, we stopped by the store on the way to the dinner, picked up some turkey burgers for me (since I don't like beef) and some gluten free buns and gluten free chips. The host was kind enough to cook my burgers on a piece of foil on the grill to avoid cross contamination and then I used my gluten free buns and chips. That way I could eat what everyone else was eating and the host was the only one who knew anything different.

Like Lisa said though, it is your health and you will realize how much better you feel when you do not have gluten. For me, it's definitely not worth it to eat anythign I'm not supposed to have!

twe0708 Community Regular
Just to build a bit on what Lisa said, too, at some point you have to not worry about whether you hurt someone else's feelings. When I first got diagnosed I was so worried about what everyone would think and whether I'd hurt my boyfriend's parents' feelings when they cooked dinner for us that I slipped up a few times just to be polite. After a couple times of that and several weeks of the aching joints, bathroom trips, headaches, fogginess, stomach pains, I decided that this is about my health. If people are going to feel bad because I want to be healthy and can't eat the cupcakes they made, it's their problem. I am not going to subject myself to a higher risk of cancer and infertility (among other potential issues!) just to make someone feel better about their cooking. Now, when I go to parties where people may not understand my disease, I take my own food or I eat before. Sometimes we call ahead if they are good friends and see exactly what they will be serving and how they are preparing it. For example, we went to a rehearsal dinner for a good friend's wedding and they just had a little cookout with burgers and brats. Well, we stopped by the store on the way to the dinner, picked up some turkey burgers for me (since I don't like beef) and some gluten free buns and gluten free chips. The host was kind enough to cook my burgers on a piece of foil on the grill to avoid cross contamination and then I used my gluten free buns and chips. That way I could eat what everyone else was eating and the host was the only one who knew anything different.

Like Lisa said though, it is your health and you will realize how much better you feel when you do not have gluten. For me, it's definitely not worth it to eat anythign I'm not supposed to have!

Thanks for your thoughts. I am not worried about hurting someone else's feelings, those are words the doctor used. I don't know why anyone in our situation were worry about what someone else thinks. If the other people don't understand then that would be their problem.

GottaSki Mentor

Doctor was definitely wrong! During my transition to gluten free it seemed reasonable that if I accidentally consumed gluten it wouldn't be a big deal as prior to gluten-free I had consumed major amounts of gluten.

Boy was I wrong!

You'll find many posts in this forum regarding people becoming extremely sensitive once gluten-free. My body attacks the smallest amount of gluten with a vengeance.

Tigercat17 Enthusiast

Hi everyone,

I have to say my doc told me pretty much the same thing. He told me after I'm heal I might be ablee to "cheat" once in a while. I know... weird? But my nutritionist (who also has celiac disease) told me not even a crumb! Sounds like a lot of doctors aren't as informed as we would like them to be and really don't know a lot about this disease.

I've been gluten free for only two weeks now so I'm pretty new to all of this. A few months ago I didn't have any symptoms. Then I started having serious acid reflux & I lost my voice the whole month of July. Then I started having stomach pains, so the doctors order the endoscopy. I've always been on the slim side & had a very big appitaite. Now I know why.

Now I'm wondering what kind of reaction I'm going to have when I get glutened by accident. It doesn't sound like fun.


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



Celiac.com Sponsor (A8-M):



GottaSki Mentor
Now I'm wondering what kind of reaction I'm going to have when I get glutened by accident. It doesn't sound like fun.

Try not to worry...you may not have severe reactions...I went undx'd for 43 years and was much more ill than my 15 year old son. I now have severe reactions, but he only feels tired with accidental glutening. Some Celiacs have little or no reaction.

Good Luck to you!

mysecretcurse Contributor

That "doctor" should lose his license to practice.

It's stuff like this that made me stop seeing doctors years ago, after they failed to tell me my problems could be caused by something I was eating. I had to find out on my own the hard way after years of suffering and thousands upon thousands of dollars spent on these "doctors" who know less than I do about celiac disease. When WE have to educate our doctors, something is VERY wrong.

angieInCA Apprentice

My Doctor actually said kind of the same thing. Said cheating every once in a while if I could tolerate it probably would hurt too much :rolleyes:

I decided to take the advice of the good people here who have lived with this disease for years and stay far far away from the stuff. Besides, for me small accidental glutenings are just terrible to deal with for days....I can't imagine doing that to myself on purpose.

heatherjane Contributor

I think the point of all this is that when it comes to celiac, sometimes we have to take our doctors' advice with a grain of salt, unless they've proven their research and knowledge to be trustworthy. I've read and heard that since celiac was once considered rare and has no cure other than diet restrictions, that most mainstream docs are simply under-informed, due to the lack of time spent studying the condition in medical school and in outside research.

If your doc is telling you something that doesn't sit right, feel free to find a new one. I'm still not 100% sold on mine, but I'm trying to give him a good year before moving to another one. We'll see.

lovegrov Collaborator

You need a new doctor.

richard

tarnalberry Community Regular

don't discount the fact that doctors will often try to find the "best" approach for their patient. not the healthiest, but the best when all things are considered. if they (rightly, based on the research that's been done on the "general celiac population") assume that you're going to find a 100% of the time gluten free diet too hard to stick to, then they may well hope that the option of having that two or three time a year "pass" will keep you gluten free the rest of the time. it's true that eating gluten only two or three times a year is far better than ignoring the gluten free diet. it's not anywhere close to as good as maintaining a strictly gluten free diet, but if your doctor doesn't think you'll do that (and patient compliance problems are always an issue in a doctor's practice), then he/she may be trying to suggest something that's better than nothing.

(no, I don't think they should go around making these assumptions. I think they're creating self-fulfilling prophecies. but I think you may get a doctor who knows 100% gluten free is the best route, but may still say this to a patient to otherwise improve compliance.)

I would probably ask the doctor *why* that advice, if I were thinking about replacing the doctor. maybe they don't know, maybe they're making bad assumptions. the latter is easier to correct (though still not always possible) than the former.

angieInCA Apprentice

My whole problem with the "alright to cheat every once in a great while" sceanario is, while we all have the best intentions to be good on our diet, if we give ourselves a pass 2 or 3 time a year, that 2 or 3 could easily and quickly turn into 4 or 5 or once a month or everyother week before one knows it.

For me, there is no other option than being strict about the diet. Lord knows I get accidentially glutened often enough, I don't need to do it on purpose.

Besides, the one thing I noticed is after a while the gluten cravings went away and even the smell of gluten isn't appitizing. By reintroducing it into my diet I would wake up the whole craving process again. It would be like breaking myself from a drug over and over and over.....what a nightmare <_<

tarnalberry Community Regular

I should have clarified - I absolutely think the doctor's advice is horrid. Absolutely dumb advice to be giving a patient. But I think it's fair to try to understand why they might say something dumber than you'd ever expect, in order to try to work past that with your doctor. It's not just useful for "treatment" of celiac, but for most other things that you may see your doctor for, since the diagnostics and prescribing they do are going to - necessarily in order to get the job done - be full of assumptions.

That said, the doctor is still giving terrible, awful, don't-ever-listen-to-it advice.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,949
    • Most Online (within 30 mins)
      7,748

    Stephanie94
    Newest Member
    Stephanie94
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
    • DebJ14
×
×
  • 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.