Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Bk Fries


pnltbox27

Recommended Posts

pnltbox27 Contributor

anybody have any reaction to ff at burger king ?i was in the other day and got a whopper no bun and a salad, i asked the manager about the friers and he told me they use dedicated friers. i personaly am not a big ff eater but i was just curious if any one else had any issues with them


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



Celiac.com Sponsor (A8-M):



MySuicidalTurtle Enthusiast

I believe they fry their onion rings in with their fries but I could be wrong.

debmidge Rising Star

I've gotten French fries that that (ooops!) a breaded onion ring in amongst the fries....

JennyC Enthusiast
I've gotten French fries that that (ooops!) a breaded onion ring in amongst the fries....

Me too. :(

The issue of what to trust is the hardest issue for me. At my home, the limited gluten that is here never touches any surface, never washed with gluten-free dishes, ect. I basically treat it as anthrax. :ph34r: But I can't bring myself to restrict my son to only eating food made at dedicated facilities on dedicated lines. SO MANY normal food companies say that they wash their lines between gluten-free and non-gluten-free foods. I take that as being sufficient but I'm not very comfortable with it. Like the Blue Diamond Nut Thins. At the health food store the guy told me that they were no longer gluten-free because it says on the box that they are made in a shared facility. I bought them anyway. They are the first gluten-free product that my son recognizes and really wants. I just think of it as they're being upfront about it, while other companies that many of us use like Frito-Lay are most likely made in a shared facility and probably on shared lines but don't state that on the package. At the risk of being cliche, it is like drawing lines in the sand.

Sorry. Needed to vent! :rolleyes:

mandasmom Rookie
Me too. :(

The issue of what to trust is the hardest issue for me. At my home, the limited gluten that is here never touches any surface, never washed with gluten-free dishes, ect. I basically treat it as anthrax. :ph34r: But I can't bring myself to restrict my son to only eating food made at dedicated facilities on dedicated lines. SO MANY normal food companies say that they wash their lines between gluten-free and non-gluten-free foods. I take that as being sufficient but I'm not very comfortable with it. Like the Blue Diamond Nut Thins. At the health food store the guy told me that they were no longer gluten-free because it says on the box that they are made in a shared facility. I bought them anyway. They are the first gluten-free product that my son recognizes and really wants. I just think of it as they're being upfront about it, while other companies that many of us use like Frito-Lay are most likely made in a shared facility and probably on shared lines but don't state that on the package. At the risk of being cliche, it is like drawing lines in the sand.

Sorry. Needed to vent! :rolleyes:

There are a wide range of opinions on this--but I do know that many, many celiacs eat(and enjoy) foods made in shared facilites...I know I say this all the time but it bears repeating--risk is part of all of our liives--celiac or not. Raising health children means attnding to their emotional and social health as well. I think eating crakers made in a shared facility is a relativley small price to pay for giving your child some choice and control in his life. In the long run--feeling ocnstantly deprived and out of control will do more harm to his overall development than the risk of a shared facility. I am meticulous about the health of my family--inlcuding myself and cleiac daughter--but i believe very very strongly that allowing as much choice and freedom as possible is part of raising healthy happy children who are confident and who reach their fullest potential. Growing celiac is tough and we owe it to our kids to be sure that we dont make it any tougher than it really is and that the restirictions we impose reflect real risk and not only parental angst...Good luck !!!!!

FeedIndy Contributor

BK fries are officially gluten free and (according to their website) always in a dedicated fryer. The problem comes when the fries are placed in a warmer right next to the onion rings. I don't like BK fries anyway so I can't tell you anything about a gluten experience.

astyanax Rookie

i can understand wanting a child to get to experience something normal like french fries at a fast food place. personally i just 100% avoid BK because, even though they said they were fried in separate friers, i kept finding onion rings in the french fries. i suggest going to any other fast food place with gluten-free fries in dedicated friers.


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



Celiac.com Sponsor (A8-M):



momandgirls Enthusiast

The website and nutritional info in the restaurants do, indeed, state that the fries are gluten free and are made in dedicated fryers. On two different occasions, in two different restaurants in two different states, I still spoke to the managers who were honest enough to tell me that, despite what the website and nutritional info state, they get busy and everything that gets fried gets thrown in together. I was disappointed but happy to know that the managers were being so honest. I even spoke to the regional manager (I wrote a letter to the corporate office and the regional manager called me) and he stated that he was not even aware of the fact that the fries were supposed to be in a dedicated fryer and, of course, had never heard of gluten or celiac. I guess what I'm saying is that we never trust fries from restaurants (I bought a deep fryer to satisfy the very infrequent craving) and we never eat in fast food restaurants - for us, it's just not worth the risk.

bigapplekathleen Contributor

I have eaten fries at at BK in Connecticut many times, and never had an issue. (Never found an onion ring, either). I have spoken with the managers there and they told me they use dedicated fryers. The onion rings are placed in a different area than the fries, too. I don't think I would trust any other BK, though! And certainly, never ever ever McDs fries.

Kat

sunshinen Apprentice

I've eaten BK fries on a few road trips and never had a problem.

mcsteffi Rookie

I have gotten ff at Burger King and found a stray onion ring. So either they fry them together or they put the in the same bin after they are cooked. I have had better luck at McDonalds than BK. Though, I have learned to say my son is allerigic to bread rather than saying wheat. I have been told many times at fast food places,,, "its white bread not wheat bread".

Stephanie

hannahsue01 Enthusiast

My daughter and I have gotten french fries a number of times from burger king and had no problems. Here they have dedicated friers. We have also had good luck at wendeys (have to check as not all Wendeys have dedicated friers....the newer ones do) and chickfalay (all there locations have dedicated friers for there waffle fries). Chickfalay has awsome gluten-free chicken breasts. Wendeys are gluten-free as well but not as good. Last I knew Burger Kings hamburgers were not gluten-free but Wendeys are. I have had bad luck with McDonalds french fries and have gotten sick every time I have tried eating them.

blueeyedmanda Community Regular

I have to say I never saw seperate fryers, and I know I have many times gotten onion rings in with my fries.

VydorScope Proficient
I have had bad luck with McDonalds french fries and have gotten sick every time I have tried eating them.

That would be likly due to the fact they are NOT on the gluten-free menu for McDonalds and have wheat listed in their ingredients....

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,269
    • Most Online (within 30 mins)
      7,748

    Jen54
    Newest Member
    Jen54
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.8k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Peggy M
      Kroeger has quite a few Gluten free items.  Right now they are redoing my Kroeger store and are adding everything into the regular sections.  Since this was done some new ones have been added.  Publix and Ingles also have great selections. I actually shop Walmart and Food City to since prices on some items vary from store to store.
    • Scott Adams
      Sorry but I don't have specific recommendations for doctors, however, starting out with good multivitamins/minerals would make sense. You may want to get your doctor to screen you for where you different levels are now to help identify any that are low, but since you're newly diagnosed within the past year, supplementation is usually essential for most celiacs.
    • trents
      Yes, I can imagine. My celiac journey started with a rejection of a blood donation by the Red Cross when I was 37 because of elevated liver enzymes. I wasn't a drinker and my family doctor checked me for hepatitis and I was not overweight. No answers. I thought no more about it until six years later when I landed a job in a healthcare setting where I got annual CMP screenings as part of my benefits. The liver enzymes were continually elevated and creeping up every year, though they were never super high. My primary care doc had no clue. I got really worried as your liver is pretty important. I finally made an appointment with a GI doc myself and the first thing he did was test me for celiac disease. I was positive. That was in about 1996. After going on a gluten-free diet for three months the liver enzymes were back in normal range. Another lab that had gotten out of whack that has not returned to normal is albumin/total protein which are always a little on the low side. I don't know what that's about, if it's related to the liver or something else like leaky gut syndrome. But my doctors don't seem to be worried about it. One thing to realize is that celiac disease can onset at any stage of life. There is a genetic component but there is also an epigenetic component. That is, the genetic component is not deterministic. It only provides the potential. There needs also to be some health or environmental stressor to activate the latent gene potential. About 40% of the population have the genetic potential to develop celiac disease but only about 1% actually do.
    • cristiana
      Hello @Heather Hill You are most welcome.  As a longstanding member and now mod of the forum, I am ashamed to say I find numbers and figures very confusing, so I rarely stray into the realms of explaining markers. (I've self-diagnosed myself with dyscalculia!)  So I will leave that to @Scott Adams or another person. However as a British person myself I quite understand that the process with the NHS can take rather a long time.  But just as you made a concerted effort to eat gluten before your blood test, I'd advise doing the same with eating gluten before a biopsy, in order to show if you are reacting to gluten.  It might be worth contacting the hospital or your GPs secretary to find out if they know what the current waiting time is. Here is a page from Coeliac UK about the current NHS recommendations. https://www.coeliac.org.uk/information-and-support/coeliac-disease/getting-diagnosed/blood-tests-and-biospy/#:~:text=If you remove or reduce,least six weeks before testing. Cristiana  
    • MI-Hoosier
      Thanks again. My mom was diagnosed over 50 years ago with celiac so grew up watching her deal with the challenges of food. I have been tested a few times prior due to this but these results have me a bit stunned. I have a liver disease that has advanced rapidly with no symptoms and an allergy that could be a contributing factor that had no symptoms. I guess I’ll call it lucky my Dr ordered a rescreen of a liver ultrasound from 5 years ago that triggered this or I would likely have tripped into cirrhosis. It’s all pretty jarring.
×
×
  • Create New...