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Question About Mcdonalds Hamburgers/salads/condition


GlutenGuy36

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GlutenGuy36 Contributor

Do you think it is safe for me to eat McDonalds hamburgers ( no bun of course , just pickles,ketchup, mustard and onion) and salad ( no croutons) with newmans own ranch dressing. I called McDonalds and they said there shouldn't be a problem with any of those. I was diagnosed back on July 14th, 2008 and only feel marginally better.

Unfortunately, I think I am one of the ones that is super sensitive to gluten now. I never was before. I am going back to the doctors soon to have my Iga levels rechecked. I was so bad I thought I had cancer of some kind. I Had tons or tests...Mri, Cat scans, hemotologist, endocrinologist even psychologist.

I have never gone through anything like this. I still feel sore inside some days are far worse than others allthough I seem to feel a little better after a bm. I feel like the toxcins are leaking into my body and making me sick. My gastro doesn't even believe in candida. I know it's only been six months but, I thought I'd see a huge improvement by now.

I live in a home where others don't have to be concerned with gluten. I am aware of the scratched pans, soaps, lotions, lip balms, places where gluten may hide. I have done my best to not to eat any allthough I know that I have eaten some accidently while on this journey.

I use to be so active now I'm relegated to my house because I feel like crap most days. If I try do the simplest of tasks I get fatigued really easily. I know that I had severe abdominal pains for 9-10 months before they even diagnosed me. I'm wondering if it will just take time to heal.

Any comments will be appreciated.


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YoloGx Rookie

I really doubt that McDonald's could accomodate you at this time. To be certain there will be cross contamination since they don't have a separate area for food prep for celiac. In addition its likely their hamburger has some kind of gluten in it to help "stretch" it. Further its possible the vinegar and pickles etc. could be a problem for you. I can't handle eating any vinegar that either isn't pure wine vinegar or Bragg's or TJ's apple cider vinegar. They say it no longer has any gluten in it but somehow it still seems to for the likes of me. Ditto with various distilled grain alcohols. Plus its likely the servers did not wash their hands before touching your plate.

I am sorry you feel ill so much still. You may need extra help to get your intestines to heal more. I suggest you try slippery elm and marshmallow root to soothe and heal the villi etc. Dandelion root taken now and then will help your liver deal with residual toxicity (avoid extracts due to the likely grain alcohol.) Cleavers or echinacea help detox the lymphatic system. Saunas and exercise also help one to detox. Eating lots of fresh veggies is really important to help detox.

Its also possible you may still be eating some things that have CC or say react to small trace amounts like in the various vinegars and pickles. And/or it may be you could could be allergic to other things in addition. This is very common with celiac due to the damaged villi allowing undigested proteins into the blood stream. Common allergens are corn, milk products (its possible/likely plain yogurt without fillers is OK), potatoes, tomatoes, green peppers, buckwheat, nuts, fermented items, sugars (I'm even allergic to fruit sugar I say sorrowfully). The last could also show a problem with candida or fungus overgrowth. I use stevia for sweetner to have something sweet without actual sugar.

Hope this helps!

Bea

Guhlia Rising Star

I eat the side salads at McDonalds with no problems. They used to have a list stating which dressings were gluten free, but it's no longer online.

Lisa Mentor

Open Original Shared Link

Here is McD's nutritional listing to include ingredients.

McD's and Chic-fil-A are the only fast food places that I will eat. I choooose carefully. ;)

tom Contributor

I'm very sure that the last time I was glutened, Mar 15 2004, was from a McD's salad I was sure was safe. I learned later that the bacon "bits" were dusted w/ flour to prevent them sticking together. Not enough to see, of course.

Don't know whether they still do that - the list at the link just says "bacon bits".

Gemini Experienced
Do you think it is safe for me to eat McDonalds hamburgers ( no bun of course , just pickles,ketchup, mustard and onion) and salad ( no croutons) with newmans own ranch dressing. I called McDonalds and they said there shouldn't be a problem with any of those. I was diagnosed back on July 14th, 2008 and only feel marginally better.

Unfortunately, I think I am one of the ones that is super sensitive to gluten now. I never was before. I am going back to the doctors soon to have my Iga levels rechecked. I was so bad I thought I had cancer of some kind. I Had tons or tests...Mri, Cat scans, hemotologist, endocrinologist even psychologist.

I have never gone through anything like this. I still feel sore inside some days are far worse than others allthough I seem to feel a little better after a bm. I feel like the toxcins are leaking into my body and making me sick. My gastro doesn't even believe in candida. I know it's only been six months but, I thought I'd see a huge improvement by now.

I live in a home where others don't have to be concerned with gluten. I am aware of the scratched pans, soaps, lotions, lip balms, places where gluten may hide. I have done my best to not to eat any allthough I know that I have eaten some accidently while on this journey.

I use to be so active now I'm relegated to my house because I feel like crap most days. If I try do the simplest of tasks I get fatigued really easily. I know that I had severe abdominal pains for 9-10 months before they even diagnosed me. I'm wondering if it will just take time to heal.

Any comments will be appreciated.

One of the biggest errors many people can make is assuming that all of their troubles are gluten related. Even though it can take a awhile for your intestines to heal, you should be feeling better by now, if your problem is just gluten. Many Celiacs also have other food intolerances or allergies, particularly to soy and dairy.

I was also extremely ill and end stage but after 3 months on the gluten-free diet, I was a new person. So I am concerned that you say you are only marginally better after 6 months....could be another intolerance. Do you notice any worsening of symptoms after consuming dairy? You may have to keep a diary or just make note when you feel badly and what you have eaten. This can be time consuming and a pain in the butt but worth the effort if you feel better.

As far as topical products go, you do not need these to be gluten-free unless you ingest them on a regular basis. Except, of course, anything that goes on the lips. Many people automatically blame topical products and it most likely is not going to be those. Candida could be another issue also and that is hard because many doctors are clueless about candida.

I would stay away, if possible, from all eating out right now. Start with the basics and see what you tolerate. Only go with companies that service the gluten-free community as a whole. I know this sounds depressing but you need to start at square one and go up from there. Maybe you could have some allergy testing done

to see if that could be an additional problem. The only other comment I could add is that you may have refractory sprue but that is rare. Did you have an endoscopy? If so, a re-check now could give you some clues as to whether you are healing well or not.

I am sorry this has been so hard for you but if you genuinely do not feel better by now, your doctor should be more willing to investigate some of the things I mentioned. Do not panic.....it may take some time but through trial and error, you can figure this out. Best of luck to you!

Mr.GlutenFree Newbie

The only thing i trust from McDonald's is there fries. Only because they use a separate fryer for them.

At home you should have a separate cabinet where all your gluten-free foods are put at. The only way i get through the day at home with two male room mates is making sure the kitchen is always clean. Also have meeting and updates for everyone, keep people involved. One of my room mates actually started a gluten-free diet just to help out and he actually liked it after a while. There's just a few ways i get through being gluten-free in a none gluten-free house. You kinda got to segregate your food from everyone else and guard it with your life, so to speak.

My doctor told me it's going to take time for the intestinal lining to heal over until you start to digest food properly. One suggestion and what i did was start taking vitamins and fiber drinks.The vitamins help with the healing process and the fiber is a cleanser for your insistent lining. It took about 3 months before i started to see results. IF you would like to know more about what vitamins i took let me know.


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larry mac Enthusiast

I eat a McD burger occassionally with no problems. But I always watch them make it, just in case they forget, put it on a bun, and then take it off. I seriously doubt that they are lying about the meat being 100% beef (ie. no fillers).

Can't say about the salads, as I rarely eat salads.

Eat the fries probably once a week.

best regards, lm

Juliebove Rising Star

I have not eaten at McDonalds in years. I do not trust them since they said they fries were vegan but contain beef. And then they didn't disclose the milk and wheat in their fries. What else are they not telling us?

If I had to eat there for some reason, I would get the apples. They are in a package and I would feel they were safe.

I do eat at Wendys and Burger King. Not the best food but it works in a pinch.

lizard00 Enthusiast

I don't do much fast food either. I find that for me, it's more "hit" than "miss". I'm pretty sensitive, too.

If I must... I eat Wendy's chili. Their fries used to be on the gluten-free list, but I tried them a few times, and every time I felt yucky after I ate them. Our family doesn't really frequent McD's, except a few occasions when my husband has to have their fries. Maybe a few times a year, at most. I have had the apples, and they're ok. They taste like apples from a bag, but they won't gluten you. ;)

I have not had much success with Chick Fil A, but they've never been a favorite of mine.

My standby is Chipotle.

lovegrov Collaborator

Fast food is a VERY bad idea if you're still having problems. Don't do it.

richard

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    • marion wheaton
      Thanks for responding. I researched further and Lindt Lindor chocolate balls do contain barely malt powder which contains gluten. I was surprised at all of the conflicting information I found when I checked online.
    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
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