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.

  • 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. - catnapt posted a topic in Related Issues & Disorders
      0

      anyone here diagnosed with a PARAthyroid disorder? (NOT the thyroid) the calcium controlling glands

    2. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      how much gluten do I need to eat before blood tests?

    3. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      Curious question

    4. - Amy Barnett posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Question

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

    • Total Members
      133,321
    • Most Online (within 30 mins)
      7,748

    Yvonne Thomas
    Newest Member
    Yvonne Thomas
    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

    • catnapt
      I am on day 13 of eating gluten  and have decided to have the celiac panel done tomorrow instead of Wed. (and instead of extending it a few more weeks) because I am SO incredibly sick. I have almost no appetite and am not able to consume the required daily intake of calcium to try to keep up with the loss of calcium from the high parathyroid hormone and/or the renal calcium leak.    I have spent the past 15 years working hard to improve my health. I lost 50lbs, got off handfuls of medications, lowered my cholesterol to enviable levels, and in spite of having end stage osteoarthritis in both knees, with a good diet and keeping active I have NO pain in those joints- til now.  Almost all of my joints hurt now I feel like someone has repeatedly punched me all over my torso- even my ribs hurt- I have nausea, gas, bloating, headache, mood swings, irritability, horrid flatulence (afraid to leave the house or be in any enclosed spaces with other people- the smell would knock them off their feet) I was so sure that I wanted a firm diagnosis but now- I'm asking myself is THIS worth it? esp over the past 2 yrs I have been feeling better and better the more I adjusted my diet to exclude highly refined grains and processed foods. I didn't purposely avoid gluten, but it just happened that not eating gluten has made me feel better.   I don't know what I would have to gain by getting a definitive diagnosis. I think possibly the only advantage to a DX would be that I could insist on gluten-free foods in settings where I am unable to have access to foods of my choice (hospital, rehab, nursing home)  and maybe having a medical reason to see a dietician?   please let me know if it's reasonable to just go back to the way I was eating.  Actually I do plan to buy certified gluten-free oats as that is the only grain I consume (and really like) so there will be some minor tweaks I hope and pray that I heal quickly from any possible damage that may have been done from 13 days of eating gluten.    
    • Jmartes71
      So I've been dealing with chasing the name celiac because of my body actively dealing with health issues related to celiac though not eating. Diagnosed in 1994 before foods eliminated from diet. After 25 years with former pcp I googled celiac specialist and she wasn't because of what ive been through. I wanted my results to be sent to my pcp but nothing was sent.I have email copies.I did one zoom call with np with team member from celiac specialist in Nov 2025 and she asked me why I wanted to know why I wanted the celiac diagnosis so bad, I sad I don't, its my life and I need revalidaion because its affecting me.KB stated well it shows you are.I asked then why am I going through all this.I was labeled unruly. Its been a celiac circus and medical has caused anxiety and depression no fault to my own other than being born with bad genetics. How is it legal for medical professionals to gaslight patients that are with an ailment coming for help to be downplayed? KB put in my records that she personally spent 120min with me and I think the zoom call was discussing celiac 80 min ONE ZOOM call.SHE is responsible for not explaining to my pcp about celiac disease am I right?
    • Amy Barnett
      What is the best liquid multivitamin for celiac disease?
    • Jmartes71
      I've noticed with my age and menopause my smell for bread gives me severe migraines and I know this.Its alarming that there are all these fabulous bakeries, sandwich places pizza places popping up in confined areas.Just the other day I suffered a migraine after I got done with my mri when a guy with a brown paper bag walk in front of me and I smelled that fresh dough bread with tuna, I got a migraine when we got home.I hate im that sensitive. Its alarming these places are popping up in airports as well.I just saw on the news that the airport ( can't remember which  one)was going to have a fabulous smelling bakery. Not for sensitive celiacs, this can alter their health during their travel which isn't safe. More awareness really NEEDS to be promoted, so much more than just a food consumption!FYI I did write to Stanislaus to let them know my thoughts on the medical field not knowing much about celiac and how it affects one.I also did message my gi the 3 specialist names that was given on previous post on questions on celiac. I pray its not on deaf door.
    • xxnonamexx
      Thanks for the info. I have been taking the ones you recommended but when I saw this I was curious if it was something else to add to the journey Thank  
×
×
  • 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.