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Fast Food


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celiacfreeman Contributor

Any one had the Burger king Chili before? I don't have any stomach problems to

tell if theres gluten in there or not. I went to Wendy's and they were out of a

baked potatoes and the taco salad and their chili. So I drove to Burger King and

guess I just took a big chance woofing down their chili. I was starving.

Ps I did not think I had any symptoms but since eating gluten free for 35 days

My iron is up to 11.4

I'm sleeping through the night

I'm not irriated by people

I can SEE at night

no need for preperation H

My skin has color again

wow

  • 4 weeks later...

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jillcole Newbie

I'm confused. I too am fairly new to this but if you go to the home page of this web site (celiac.com) and go to the link 'mainstream products that are gluten-free' it has a ton of candy. Butterfingers, snickers and a lot more. There are a ton of gluten-free brownie recipes and mixes. Certainly enough to cure any sweet tooth. I have printed off all the safe and forbidden food lists but both my son & I (mostly me) find this diet fairly easy. I feel like I have a good grasp on what is legal but now I am concerned. Am I missing something?

Also a wonderful recipie for fried chicken breast is as follows:

1. Dust your chicken with a legal flour

2. Roll it in soaked ground flaxseed. (2 tablespoons of ground flaxseed and 2/3

cup of lukewarm water. Give this mix time to absorb. 4 to 5 minutes.

3. roll it in brown rice bread crumbs. I have only used HOL-GRAIN bread crumbs.

4. Then put in in your pan with olive oil, salt it and cook it. Make sure you have

enough HOT oil so your chicken does not stick.

This is a 5 star out of 5. I make it for company & they love it.

  • 2 weeks later...
Debbierb Newbie

Hi

I'm a newly diagnosis celiac (4 weeks) and I found this board when my doctor said he suspected I had celiac disease after an endoscopy. (Of course since then the biopsy and blood test were positive) Since I had never heard of it I immediately turned to the internet and found this site.

After reading a lot of the messages and info I was really excited to have a place to talk to people and learn from people who have had a lot more experience then me.

In all the reading here I've done, I learned of a site www.safetoeat.net that had a list of items that are safe at different fast food places and I also learned about the Outback.

I have to tell you, today was the first day I was really feeling down (pretty depressed) since my diagnosis. It could have to do with the fact that I went for a family birthday gathering at a pizza place last night. This had already been set up before my family new about me having celiac disease and there was nothing I could eat except salad. I hate salads!

This morning my daughter kept after me to take her to the mall and so I finally agreed to do it and I thought 'I need to eat before we go' so I don

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    • MoniqueCham
      Thanks for your reply Scott! A long time ago I realized I didn’t fit neatly into uncomplicated celiac disease. Over the years I’ve been diagnosed and treated for SIBO, pancreatic insufficiency and diagnosed with Stage 2 liver fibrosis. I think all the complications occurred because of the refractory celiac disease. When I hit menopause my gut issues seemed to calm down and because I was stable I made the mistake of not following up with my gastroenterologist. Then other autoimmune problems flared and I tried the methotrexate. It worked like a charm for my skin condition… then my sigmoid colon ruptured. Strange but my autoimmune skin condition remains in remission after 6 months off the medication. We have a very long waiting list to get back into see my GI doctor… I was an emergency referral but am still waiting 6 months after the perforation. I need more surgery to fix a fistula that has formed and to reconnect my colon… I have a colostomy at present. I became a dietitian who specializes in bowel diseases but have never met anyone who’s had so many complications with celiac disease. I have a brother and son who also have been diagnosed. My mother had 4 autoimmune diseases including a vasculitis that eventually resulted in her death and it was my father who had the HLA DQ2 gene. Think I inherited some tendencies from each of them. Thanks again for your response… it feels a little lonely dealing with GI issues when I work so hard to remain gluten free.   
    • HelenH
      Thank.you both
    • Scott Adams
      Yes, unfortunately malt vinegar can definitely trigger a strong reaction in people with celiac disease. Malt vinegar is typically made from barley, which contains gluten, and unlike distilled white vinegar, it is not considered gluten-free. Even a small amount — especially if you’ve been strictly gluten-free for years — can cause a more intense reaction because your body is no longer accustomed to exposure. Many people report significant symptoms after accidental ingestion, including abdominal pain, diarrhea, fatigue, or flu-like feelings. You’re not alone in that experience. It may help to be especially cautious with salad dressings, chips, sauces, and restaurant foods, where malt vinegar is sometimes used.
    • Scott Adams
      A diagnosis of Refractory Celiac Disease Type 2 is a lot to absorb, especially if you feel like the severity wasn’t clearly communicated earlier. It’s understandable to feel shocked and frustrated. RCD Type 2 does require close specialist care, often with a gastroenterologist who has experience managing complex celiac cases, and sometimes coordination with hematology because of the immune cell changes involved. Focusing on nutrition is absolutely important — many people benefit from working with a registered dietitian who specializes in celiac disease to help address malabsorption, weight loss, and vitamin or mineral deficiencies. You’re doing the right thing by seeking information and support. Make sure you feel comfortable asking your care team direct questions about your biopsy results, treatment plan, and monitoring strategy — you deserve clarity and a coordinated approach.
    • Scott Adams
      I’m so sorry you’ve been through all of that — that’s an incredibly complex history. While methotrexate is widely used at low weekly doses for autoimmune conditions, it can, in rare cases, cause serious gastrointestinal side effects, including ulceration, mucosal injury, or even perforation. That said, a spontaneous sigmoid rupture from methotrexate at 15 mg weekly is extremely uncommon. In people with celiac disease — especially refractory celiac — there can already be underlying intestinal inflammation or altered mucosal integrity, which might theoretically increase vulnerability, but there isn’t strong published evidence clearly linking stable celiac disease to a markedly higher risk of methotrexate-related bowel perforation. Other factors such as concurrent inflammation, vascular compromise, infection, steroid use, or microscopic colitis may also contribute. It would be reasonable to review the case with a gastroenterologist familiar with refractory celiac and possibly a rheumatologist, and to report the event as a potential adverse drug reaction. I’d also be very interested to hear if others in the community have had similar experiences.
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