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

Wendys Frostys


mmichaud87

Recommended Posts

mmichaud87 Newbie

I have been reading different posts on here about Wendys frostys being gluten free.

I had a question for anyone who might have an answer. Has anyone had a negative reaction after having the frosty. My 5 yr old son and mother in law are both on gluten free diets for celiacs. Today, all of us(my wife, son, mother in law and I) had a frosty. My son and mother in law, within an hour, were both extremely sick. It has been almost 12 hours since they had the frosty, my son is a little better, still has a stomach ache, but my mother in law is still sick. We know it wasnt a bad batch because my wife and I are fine. We called my sons specialist and she said based on his symptoms, it was a reaction to gluten, but I thought they were supposed to be gluten free.

Any help on what to do would be greatly appreciated.


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



Celiac.com Sponsor (A8-M):



still tiredofdoctors Rookie

I thought they were supposed to be gluten-free, too. My reaction to gluten is so delayed (neurogenic vs. gut) that I'm not someone to run immediate reaction by. I'll ask my home health nurse. Her celiac is severe and her sensitivity is almost hair-trigger. She is constantly reading about gluten-free status of foods, and is a really valuable resource. She is coming on Monday. I'll get back with you then.

Judyin Philly Enthusiast
I thought they were supposed to be gluten-free, too. My reaction to gluten is so delayed (neurogenic vs. gut) that I'm not someone to run immediate reaction by. I'll ask my home health nurse. Her celiac is severe and her sensitivity is almost hair-trigger. She is constantly reading about gluten-free status of foods, and is a really valuable resource. She is coming on Monday. I'll get back with you then.

Lynne.....so happy to see you

no on here much anymore but had to say HI

About Wendy's ........I thought they were gluten-free also but i had to stop eating there as even the potato was cc. and after i year of successful eating at wendy's i had to stop.

Maybe someone can ck their web site and see what they are saying now. I havent' looked at it in over a year. I still think the cc there is the worst.

amybeth Enthusiast

They've recently started adding things (cookies?) to some of their frosty's...maybe it's a cc thing now that other ingredients are in the mix...so to speak.

mmichaud87 Newbie

Thank you everyone for the replys. I did check their website. It still says that Frostys are gluten free. But I was wondering about the cc as well. Someone from the company is supposed to be contacting me about this today or tomorrow. When I hear more I will let everyone know,again thank you

Ahorsesoul Enthusiast

I always had problems with their frosty's but haven't tried one for several years. Not likely to do so soon either.

hermitgirl Contributor

CC is a major issue at Wendy's. I have watched at two locations while food is being prepared, and won't eat there. The buns are stored right next to the potatoes at these locations, the person who handles both does not change gloves in between, and got rather crabby about being asked to do so. As far as the frostys, now that they have all these new things with them, do each come out of seperate machines? If not, there is no way to prevent the cross contamination as they aren't going to take the time after each frosty to clean all the shared parts. I gave up on them shortly after being diagnosed. I have gotten sick every time.


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



Celiac.com Sponsor (A8-M):



Ahorsesoul Enthusiast

I have no trouble with blizzards from my local Dairy Queen. I am very sensitive to cc so I'm surprised that I do not have to ask at DQ for them to wipe down the equipment an extra time or to wash their hands before making my blizzard.

I wish I could say this about all fast food places.

heathen Apprentice

I react to Wendy's frosties because of my lactose intolerance--so I order the Junior frosty. Not only is it a very small portion that is cool and chocolatey, but it is also cheaper and doesn't aggravate the lactose intolerance. however, I would stear clear of the shakes--too much risk of contamination.

Lisa Mentor

For those that are newly diagnosed, a good dose of dairy can simulate gluten symtoms.

lizzibug21 Newbie

I eat frostys ALOT more often then I should, and haven't had any issues

brendygirl Community Regular

I always eat frostys. Never had a reaction. I don't eat any sort of potato or fries there, because cc. I only eat fries at Chic-Fil-A and In-n-out.

  • 1 year later...
mingo Newbie

I have been reading different posts on here about Wendys frostys being gluten free.

I had a question for anyone who might have an answer. Has anyone had a negative reaction after having the frosty. My 5 yr old son and mother in law are both on gluten free diets for celiacs. Today, all of us(my wife, son, mother in law and I) had a frosty. My son and mother in law, within an hour, were both extremely sick. It has been almost 12 hours since they had the frosty, my son is a little better, still has a stomach ache, but my mother in law is still sick. We know it wasnt a bad batch because my wife and I are fine. We called my sons specialist and she said based on his symptoms, it was a reaction to gluten, but I thought they were supposed to be gluten free.

Any help on what to do would be greatly appreciated.

I have been Gluten Free for 2 weeks now and have never felt better! At the age of 46, being sick had become a wa of life, I feel like a new person. Last night I ate a Wendy's Frosty. Just like your wife and Mother in law, I became ill within an hour. It is now 10 plus hour later and I am still sick at my stomach. I have never been lactose int either. What the heck is in the frosty? I won't be eating anymore>

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,134
    • Most Online (within 30 mins)
      7,748

    Driver
    Newest Member
    Driver
    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

    • Sarah Grace
      Dear Kitty Since March I have been following your recommendations regarding vitamins to assist with various issues that I have been experiencing.  To recap, I am aged 68 and was late diagnosed with Celiac about 12 years ago.  I had been experiencing terrible early morning headaches which I had self diagnosed as hypoglycaemia.  I also mentioned that I had issues with insomnia, vertigo and brain fog.   It's now one year since I started on the Benfotiamine 600 mg/day.  I am still experiencing the hypoglycaemia and it's not really possible to say for sure whether the Benfotiamine is helpful.  In March this year, I added B-Complex Thiamine Hydrochloride and Magnesium L-Threonate on a daily basis, and I am now confident to report that the insomnia and vertigo and brain fog have all improved!!  So, very many thanks for your very helpful advice. I am now less confident that the early morning headaches are caused by hypoglycaemia, as even foods with a zero a GI rating (cheese, nuts, etc) can cause really server headaches, which sometimes require migraine medication in order to get rid off.  If you are able to suggest any other treatment I would definitely give it a try, as these headaches are a terrible burden.  Doctors in the UK have very limited knowledge concerning dietary issues, and I do not know how to get reliable advice from them. Best regards,
    • knitty kitty
      @rei.b,  I understand how frustrating starting a new way of eating can be.  I tried all sorts of gluten-free processed foods and just kept feeling worse.  My health didn't improve until I started the low histamine AIP diet.  It makes a big difference.   Gluten fits into opioid receptors in our bodies.  So, removing gluten can cause withdrawal symptoms and reveals the underlying discomfort.  SIBO can cause digestive symptoms.  SIBO can prevent vitamins from being absorbed by the intestines.  Thiamine insufficiency causes Gastrointestinal Beriberi (bloating, abdominal pain, nausea, diarrhea or constipation).  Thiamine is the B vitamin that runs out first because it can only be stored for two weeks.  We need more thiamine when we're sick or under emotional stress.  Gastric Beriberi is under recognised by doctors.  An Erythrocyte Transketolace Activity test is more accurate than a blood test for thiamine deficiency, but the best way to see if you're low in thiamine is to take it and look for health improvement.  Don't take Thiamine Mononitrate because the body can't utilize it well.  Try Benfotiamine.  Thiamine is water soluble, nontoxic and safe even at high doses.  I thought it was crazy, too, but simple vitamins and minerals are important.  The eight B vitamins work together, so a B Complex, Benfotiamine,  magnesium and Vitamin D really helped get my body to start healing, along with the AIP diet.  Once you heal, you add foods back in, so the AIP diet is worth doing for a few months. I do hope you'll consider the AIP diet and Benfotiamine.
    • captaincrab55
      Imemsm, Most of us have experienced discontinued, not currently available or products that suddenly become seasonal.   My biggest fear about relocating from Maryland to Florida 5 years ago, was being able to find gluten-free foods that fit my restricted diet.  I soon found out that the Win Dixie and Publix supper markets actually has 99% of their gluten-free foods tagged, next to the price.  The gluten-free tags opened up a  lot of foods that aren't actually marked gluten-free by the manufacture.  Now I only need to check for my other dietary restrictions.  Where my son lives in New Hartford, New York there's a Hannaford Supermarket that also has a gluten-free tag next to the price tag.  Hopefully you can locate a Supermarket within a reasonable travel distance that you can learn what foods to check out at a Supermarket close to you.  I have dermatitis herpetiformis too and I'm very sensitive to gluten and the three stores I named were very gluten-free friendly.  Good Luck 
    • rei.b
      Okay well the info about TTG-A actually makes a lot of sense and I wish the PA had explained that to me. But yes, I would assume I would have intestinal damage from eating a lot of gluten for 32 years while having all these symptoms. As far as avoiding gluten foods - I was definitely not doing that. Bread, pasta, quesadillas (with flour tortillas) and crackers are my 4 favorite foods and I ate at least one of those things multiple times a day e.g. breakfast with eggs and toast, a cheese quesadilla for lunch, and pasta for dinner, and crackers and cheese as a before bed snack. I'm not even kidding.  I'm not really big on sugar, so I don't really do sweets. I don't have any of those conditions.  I am not sure if I have the genes or not. When the geneticist did my genetic testing for EDS this year, I didn't think to ask for him to request the celiac genes so they didn't test for them, unfortunately.  I guess another expectation I had is  that if gluten was the issue, the gluten-free diet would make me feel better, and I'm 3 months in and that hasn't been the case. I am being very careful and reading every label because I didn't want to screw this up and have to do gluten-free for longer than necessary if I end up not having celiac. I'm literally checking everything, even tea and anything else prepacked like caramel dip. Honestly its making me anxious 😅
    • knitty kitty
      So you're saying that you think you should have severe intestinal damage since you've had the symptoms so long?   DGP IgG antibodies are produced in response to a partial gluten molecule.  This is different than what tissue transglutaminase antibodies are  produced in response to.   TTg IgA antibodies are produced in the intestines in response to gluten.  The tTg IgA antibodies attack our own cells because a structural component in our cell membranes resembles a part of gluten.  There's a correlation between the level of intestinal damage with the level of tTg antibodies produced.  You are not producing a high number of tTg IgA antibodies, so your level of tissue damage in your intestines is not very bad.  Be thankful.   There may be reasons why you are not producing a high quantity of tTg IgA antibodies.  Consuming ten grams or more of gluten a day for two weeks to two months before blood tests are done is required to get sufficient antibody production and damage to the intestines.  Some undiagnosed people tend to subconsciously avoid lots of gluten.  Cookies and cakes do not contain as much gluten as artisan breads and thick chewy pizza crust.  Anemia, diabetes and thiamine deficiency can affect IgA antibody production as well.   Do you carry genes for Celiac?  They frequently go along with EDS.
×
×
  • 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.