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

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
      131,855
    • Most Online (within 30 mins)
      7,748

    Tara M
    Newest Member
    Tara M
    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

    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
    • Francis M
      Thanks. Since the back and forth and promises of review and general stalling went on for more than six months, the credit company will no longer investigate. They have a cutoff of maybe six months.
    • Scott Adams
      Is this the same restaurant? https://www.facebook.com/TheHappyTartFallsChurch/ Is it too late to take this up with your credit card company? Normally you have a few months to do a chargeback with them. It seems very odd that they are taking this approach with someone who is likely to be a regular customer--not a good business-minded way of handling things!
    • Scott Adams
      Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: The most common nutrient deficiencies associated with celiac disease that may lead to testing for the condition include iron, vitamin D, folate (vitamin B9), vitamin B12, calcium, zinc, and magnesium.  Unfortunately many doctors, including my own doctor at the time, don't do extensive follow up testing for a broad range of nutrient deficiencies, nor recommend that those just diagnosed with celiac disease take a broad spectrum vitamin/mineral supplement, which would greatly benefit most, if not all, newly diagnosed celiacs. Because of this it took me decades to overcome a few long-standing issues I had that were associated with gluten ataxia, for example numbness and tingling in my feet, and muscle knots--especially in my shoulders an neck. Only long term extensive supplementation has helped me to resolve these issues.        
×
×
  • 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.