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

Gluten Free Pizza


Booghead

Recommended Posts

Booghead Contributor

Before being diagnosed about 2 weeks ago I would sell my soul for Pizza Hut Supreme Pan Pizza. I love it so much. SO MUCH. I was wondering if you guys had any recipes for really good pan pizza crust or pizza sauce. I heard you have to drown gluten free pizza crust in sauce because it all gets absorbed. I love pizza so much. How do I get that oily and greasy, deep fried taste of pizza hut? Please help? lol


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



Celiac.com Sponsor (A8-M):



Takala Enthusiast

Uhm, ah, what does this stuff taste like ? :o:ph34r:

How do I get that oily and greasy, deep fried taste of pizza hut? Please help? lol

If you want a crust that is sort of grease- crusted, you would lay a lot of olive oil down in the pizza pan first, maybe sprinkle with some gluten free cornmeal, then put the dough in it to bake until almost done. THEN you would put the toppings on it to finish it off, but you'd spread the top surface of the dough first with olive oil, then add the sauce, cheese, and toppings, then run it under the broiler again.

Alternatively, you could use a dedicated cast iron pan for gluten free cooking, and preheat it w/ olive oil, then add your crust, then it would bake/fry, but getting the pizza crust into the hot oiled pan would be a little tricky. You can preheat the pan on the stovetop burner. But that is another way to get a crispy fried bottom crust.

sa1937 Community Regular

I hear you, Booghead! I used to love Pizza Hut Supreme Pan Pizza, too, but now make my own. It's not Pizza Hut but it's good and and it satisfies my pizza cravings but I don't make it greasy. Takala has given you some good suggestions for that. And no, you don't have to drown a gluten-free pizza crust in sauce. The only time I had trouble with that was when I used gluten-free Bisquick for a crust.

You might want to check this recent pizza crust thread and see if you can find a recipe that appeals to you.

Marilyn R Community Regular

Before being diagnosed about 2 weeks ago I would sell my soul for Pizza Hut Supreme Pan Pizza. I love it so much. SO MUCH. I was wondering if you guys had any recipes for really good pan pizza crust or pizza sauce. I heard you have to drown gluten free pizza crust in sauce because it all gets absorbed. I love pizza so much. How do I get that oily and greasy, deep fried taste of pizza hut? Please help? lol

The most palatable crust I've found is the pizza mix by Chebes, which a local health food store sells for less than $3, & the gluten-free mall carries it. There are a few gluten-free bloggers that have recreated the mix by using tapioca flour, etc., but I haven't tried that yet. If you check the ingredients on pizza sauce, they should be great. There's an organic one the I like available locally.

Get one of those holy pizza pans at Wal-Mart. $12.

SUPER SUPREME PIZZA

A feast of pepperoni, ham, beef, pork sausage, Italian sausage, red onions, mushrooms, green peppers and black olives.

I pasted that from Pizza Hut's web site, it should all be safe, but check ingredients. Just remember that when you're making pizza everything is in little bits, so unless you have other plans for those toppings, I'd trim it down a bit.

I had an unfortunate former marriage to someone who owned a pizza parlor, so I've had a LOT of pizza. My favorite is sausage, mushrooms and onion on a thin crust with lots of cheese. You can cook pizza in the oven (follow directions on the Chebe package) or grill it, it's yummy.

I'm not doing corn. Here's how I make pizza.

Make Chebe mix according to directions. Once rolled out(or patted, if you don't have a rolling pin), use a soup spoon to apply pizza sauce, and use the back of it to smooth it over the crust. You want to see some white on the crust, don't put the sauce on too thickly. Scatter your minced/chopped ingredients on the crust. Top with freshly shredded mozzarella cheese and some grated parmesan cheese. Drizzle a little olive oil over the top. Add S&P and Italian spices if desired and bake or grill per pkg. instructions.

I don't even bother reheating the leftovers, eat 'em cold. There's an older thread about pizza if you search, so maybe somebody has a better recipe than this one, but I'm really happy with this one.

Reba32 Rookie

Boston Pizza has a gluten free pizza that is a little like the Pizza Hut pan pizza

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,962
    • Most Online (within 30 mins)
      7,748

    AlissaW
    Newest Member
    AlissaW
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.