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

U.s. Policies Around Gluten & Other Food Allergens


lucia

Recommended Posts

lucia Enthusiast

Hi everyone,

I'm in the advanced stages of my recovery from gluten intolerance/celiac, thanks to a combination of strict dietary regulation (including the Specific Carbohydrate diet) and Traditional Chinese Medicine (both acupuncture and herbs). I'm so grateful for my recovery. I was able to take a vacation last week to Rome and Florence to see the sights and to the U.K. to visit my godchild. A great trip, especially after such a difficult year.

I find myself wondering though: why have the governments of both Italy and the U.K. instituted policies that address people's medical issues with gluten, but my government has not.

In Italy, gluten-free foods are available in every pharmacy, right next to the diabetic foods. The government mandates this. In restaurants, when I described myself as a celiac or asked for gluten-free food, my servers were serious about accommodating my needs. Sometimes, I was turned away from a restaurant, but I was not served food with gluten. Given the seriousness with which my servers treated me, I wondered if the government also holds restaurants responsible for what they serve people? Of course, in a country with so much awareness of celiac, gluten-free goods were also readily available in supermarkets and restaurants with gluten-free menus were easy to find.

In the U.K., every packaged food product is labelled as to its allergens, including gluten (but also wheat, soy, milk, etc. and even celery). Even all prepared foods, such as soups and salads, are labelled. I can't comment on eating in restaurants, since on our short trip, I ate only prepackaged, prepared foods and home-cooked meals. But, also, on British Air, I was served a gluten-free dinner without any fuss.

Laws requiring 1) labels alerting consumers to food allergens, and 2) availability of gluten-free goods in pharmacies seem like solutions that are both simple and effective for people like us who struggle with a gluten-free diet. These measures also seem like they'd be no sweat off the backs of the politicians who get them passed. So, what's the hold-up in the U.S.? I know that the American medical community is hardly as responsive about diagnosing celiac/gluten intolerance as their peers in Europe, but still - isn't it so often consumer-led groups that get bills passed in the U.S.? Is there a lobbying group of celiacs out there that is working to get measures like these passed? Or is this the kind of thing that will be taken seriously only if it's led by doctors?

And, most importantly, what can I do to support such policies?


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



Celiac.com Sponsor (A8-M):



tarnalberry Community Regular

Part of the reason is political - it *is* a big sweat off the politicians backs, because the agriculture business has a HUGE lobby with a LOT of money paying them to keep things easy. Not to mention the lawsuit fears that are rampant in this country. Write to your congress people and voice support of *reasonable* legislation (even if it's not the ideal of what you'd like). And vote with your pocketbook in places that make things as much like you would prefer as possible.

love2travel Mentor

I understand your frustration. In Canada we are even behind the U.S.! In preparation for a recent trip to Italy and Croatia I discovered that testing for celiac disease for every single person in Italy is mandatory by the age of 5. Amazing. It was interesting eating out in Italy; at a gelateria I was told I definitely could not have any of the gelato (Venice) but I could have the granita (delicious - I love granita). The employee even got the list of ingredients out to show me. Their knowledge was incredible. Rather than being met with blank stares, employees are so well versed in gluten-free. Croatia was not as easy but still easier than Canada (at least where I live where there are literally ZERO eateries I can eat at). Restaurant cards helped. Good to know that those of us with celiac disease are able to continue to safely eat in Europe!

ravenwoodglass Mentor

Part of the reason is political - it *is* a big sweat off the politicians backs, because the agriculture business has a HUGE lobby with a LOT of money paying them to keep things easy. Not to mention the lawsuit fears that are rampant in this country. Write to your congress people and voice support of *reasonable* legislation (even if it's not the ideal of what you'd like). And vote with your pocketbook in places that make things as much like you would prefer as possible.

In addition to this we also have Big Pharma who would rather sell us meds for symptoms. Over just the last 10 to 20 years or so a lot of the meds to control celiac related symptoms have gone to OTC so folks self medicate instead of insisting on a diagnosis of what is really wrong. We are actually taught from a young age that we should take a pill rather than finding out what the cause is. Many think feeling ill is 'normal for them'. That means lot of money lost when folks no longer need daily immodium, laxatives and meds for stomach pain, headaches, psychological and learning problems etc. In the US they give us pills to control symptoms rather than figuring out the cause.

ErinP Newbie

I think big pharma does indeed have a LOT to do with it, but--

Part of the reason is political - it *is* a big sweat off the politicians backs, because the agriculture business has a HUGE lobby with a LOT of money paying them to keep things easy.

I think this is the primary reason right here.

Despite the fact that grains are the most caloric-dense, and least nutritive of almost any food we consume, that they comprise the BASE of the US's food pyramid should be clue #1.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,806
    • Most Online (within 30 mins)
      7,748

    MoonBear
    Newest Member
    MoonBear
    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

    • Scott Adams
      What you've described—the severe weight loss, the cycle of medications making things worse, and the profound fear of eating before leaving the house—is a heavy burden to carry for 15 years. It is absolutely not your fault. While everyone's journey with celiac is different, the struggles with the learning curve, social isolation, and dietary grief are feelings many in the community know all too well. Your question about whether you should just eat what you want and manage the symptoms is a heartbreaking one, born from years of frustration. It's crucial to know that the diarrhea is a sign of ongoing damage to your small intestine from gluten, and simply managing the symptom with Imodium doesn't stop that internal harm or the risk of other complications. The fact that you are still getting sick within an hour of eating, even while trying to be gluten-free, is a huge red flag that something isn't right. This could be due to cross-contamination in your kitchen (e.g., using a shared toaster, colander, or condiment jars), hidden gluten in foods, or the possibility of another concurrent condition like refractory celiac disease. Don't give up!  This article has some detailed information on how to be 100% gluten-free, so it may be helpful (be sure to also read the comments section.):    
    • KathyR37
      I am new here but celiac disease is not new to me. I was diagnosed with it at age 60. At the time I weighed a whopping 89 pounds. I was so ignorant to celiac so I buried myself in learning all about it and looking for food I could eat. I lost so much weight and stayed sick all the time. So to combat the sickness I was give all sorts of meds for loose bowels and vomiting. All that just made me sicker. Eventually I chucked it all and went back to eating like I had all my life. Now I am from the south and biscuits and gravy are a big part of our food, as are breaded foods, pasta, and sandwich bread. Through the years I would try to do the gluten free thing again and am doing it now. It has not helped any. Within and hour of eating I have to run to the bathroom. I am now 75 and am wondering if I should just forget it and eat what I like, take Immodium and live the best I can. I cannot eat before going anywhere for fear of embarrassing myself. Family and church dinners are out of the question unless I eat and run straight home. I am so frustrated I just want to sit down and cry or throw something. Does everyone go through all this?
    • Scott Adams
      This article, and the comments below it, may be helpful:    
    • nanny marley
      Oh yes I can understand the tiredness after going threw all that, must be exhausting especially on the mind I have high aniexty so I can understand that , I wish there more easier ways for people to get help , I had a MRI on my spine some years ago without anything it was really quick and no prep , I understand the need for  them to see better with the bowel ,but you think they would use something a little less traumatic  for ibd sufferers on the bowels by now ,I hope your feeling better today 🙏
    • Colleen H
      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..  
×
×
  • 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.