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

Pizza Fusion

Alphawave

By Alphawave
in Gluten-Free Restaurants

Recommended Posts

Alphawave Rookie
Alphawave
Posted

Anyone who has Pizza Fusion in their state, have you tried the gluten-free crust? We just had a restaurant move into HOuston, right in my area, and was wanting to know if you liked the pizzas.

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

Celiac.com Sponsor (A8-M):


Coleslawcat Contributor
Coleslawcat
Posted

Anyone who has Pizza Fusion in their state, have you tried the gluten-free crust? We just had a restaurant move into HOuston, right in my area, and was wanting to know if you liked the pizzas.

I went there before I was diagnosed so I didn't try the gluten free crust. I had a regular crust pizza and I liked it. I hear they use Tom Sawyer flour for their pizza crusts. In Arizona there is 1 company that supplies gluten free crusts to a few different chains, they use the Tom Sawyer flour, I have had one of those from Barro's Pizza and it was good. I'm not sure it's the same crust Pizza Fusion in Houston would use, but they are the same supplier for our local Pizza Fusion.

babinsky Apprentice
babinsky
Posted

Anyone who has Pizza Fusion in their state, have you tried the gluten-free crust? We just had a restaurant move into HOuston, right in my area, and was wanting to know if you liked the pizzas.

I have had their pizza a few times....I think it is pretty good.

gaingus Rookie
gaingus
Posted

I have had their gluten free pizza and the brownie that they offer and I like them both pretty well. Since it is an hours drive to the nearest one where I am at here in Ca, and the cost, we don't go very often. B)

Alphawave Rookie
Alphawave
Posted
  • Author

I have had their gluten free pizza and the brownie that they offer and I like them both pretty well. Since it is an hours drive to the nearest one where I am at here in Ca, and the cost, we don't go very often. B)

Thanks for the input. I couldn't believe it when I found out this is the first Pizza Fusion in Texas, let alone Houston, and here it is 2 miles away. I am supposing that they are a bit pricey. But I haven't had a pizza FOREVER !!!!!

gaingus Rookie
gaingus
Posted

The one I have here sells gluten free beer too. It is the more expensive Greene;s brand but it was good to have pizza and a cold beer together.

Alphawave Rookie
Alphawave
Posted
  • Author

The one I have here sells gluten free beer too. It is the more expensive Greene;s brand but it was good to have pizza and a cold beer together.

That sounds great! I have only tried Redbridge beer, so that would be something different for me!

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

Celiac.com Sponsor (A8-M):


nutrifoodie Apprentice
nutrifoodie
Posted

I personally wouldn't go back to Pizza Fusion. I went to the San Diego location. The pizza was mediocre. It was made with Bob's Red Mill and you could tell it WAS gluten free - very bean tasting. The whole pizza was not tasty at all - it totally lacked flavor. It was also a $30 pizza - which is RIDICULOUS. I am not going back. I can seriously make a pizza 20X better at home.

MonKol Rookie
MonKol
Posted

I have been to the one on Biscayne in Miami and thought the Pizza was amazing, especially as I hadn't had any pizza for a few months BUT it is disgustingly expensive for the size of it. It comes in a large only, which is a good job because it's not a large you are used to. It really is a "restaurant" not a pizza joint like you would expect. It is fancy, nice furniture, nice wine list etc etc. I also had the brownies, the manager gave us extra too which was a bonus because they were yummy!

I have to admit, despite the great taste (crust tasted more like a regular flour crust) the nice setting and great brownies, I haven't been back. It's down to the cost and it's just too expensive. This is a case when I truly feel they are jacking up the price to take advantage for a limited market in a restaurant setting, not a pizza place setting. Much like Amy's and Glutino's frozen ones. I can buy the corn flour and make it myself for the SAME price as if I was to make it with regular flour.

I did however go to Slice in Ft Lauderdale this past weekend and spoke to the part owner, Aaron Carter (yes the dancing with the stars, backstreet boy baby brother and teen heartthrob) and asked him about a gluten free pizza... his words were "it's done" so watch this space!!! hopefully we will have a true pizza parlor that caters to gluten free slice lovers!!!

Swerd1 Newbie
Swerd1
Posted

The one I have here sells gluten free beer too. It is the more expensive Greene;s brand but it was good to have pizza and a cold beer together.

Same with the one by me. It's not my favorite, but better than nothing!

msmini14 Enthusiast
msmini14
Posted

Same with the one by me. It's not my favorite, but better than nothing!

First time posting since they changed the site, so hope this works right.

I will never go back to that place, way over priced for what you get. And to be honest, when I ate there I had terrible terrible gas and I had my pizza made with soy cheese.

Archived

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

Go to topic listing

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate
  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):



    Celiac.com Sponsors (A17-M):



  • Recent Activity

    1. cristiana
      - cristiana replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

      I agree, it so often overlooked! I live in the UK and I have often wondered why doctors are so reluctant to at least exclude it - my thoughts are perhaps the particular tests are expensive for the NHS, so therefore saved for people with 'obvious' symptoms. I was diagnosed in 2013 and was told immediately that my parents, sibling and children should...
    2. chrisinpa
      - chrisinpa commented on Scott Adams's article in Skin Problems and Celiac Disease
      2

      Celiac Disease and Skin Disorders: Exploring a Genetic Connection

      Maybe they can attribute certain skin conditions to either being susceptible to getting Celiac......or the other way around....but I have to ask if certain people are prone to Celiac because of genetics and some people aren't. It's kind of the same thing as what came first.....the chicken or the egg.?
    3. knitty kitty
      - knitty kitty replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      My journey is it gluten or fiber?

      @xxnonamexx, There's labeling on those Trubar gluten free high fiber protein bars that say: "Manufactured in a facility that also processes peanuts, milk, soy, fish, WHEAT, sesame, and other tree nuts." You may want to avoid products made in shared facilities. If you are trying to add more fiber to your diet to ease constipation, considering...
    4. trents
      - trents replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

      Welcome to celiac.com @sha1091a! Your experience is a very common one. Celiac disease is one the most underdiagnosed and misdiagnosed medical conditions out there. The reasons are numerous. One key one is that its symptoms mimic so many other diseases. Another is ignorance on the part of the medical community with regard to the range of symptoms that celiac...
    5. trents
      - trents commented on Jefferson Adams's article in Other Diseases and Disorders Associated with Celiac Disease
      6

      Celiac Disease Patients Face Higher Risk of Systemic Lupus

      What kind of practitioner did the blood test? Was this a medical doctor, a naturopathic doctor, a GI doc? I would certainly follow up with them and ask why they advised you not to eat red meat. I mean, it could be something like they, themselves, are a vegetarian and give that advice to everyone. Have you had an endoscopy with biopsy of the small bowel...
  • Celiac.com Sponsor (A19):

  • Member Statistics

    • Total Members
      132,692
    • Most Online (within 30 mins)
      7,748
    Ali Zaib
    Newest Member
    Ali Zaib
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):

  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):

  • Upcoming Events

  • Posts

    • cristiana
      Issues before diagnosis

      By cristiana · Posted

      I agree, it so often overlooked! I live in the UK and I have often wondered why doctors are so reluctant to at least exclude it - my thoughts are perhaps the particular tests are expensive for the NHS, so therefore saved for people with 'obvious' symptoms.  I was diagnosed in 2013 and was told immediately that my parents, sibling and children should be checked.  My parents' GP to this day has not put forward my father for testing, and my mother was never tested in her lifetime, despite the fact that they both have some interesting symptoms/family history that reflect they might have coeliac disease (Dad - extreme bloating, and his Mum clearly had autoimmune issues, albeit undiagnosed as such; Mum - osteoporosis, anxiety).  I am now my father' legal guardian and suspecting my parents may have forgotten to ask their GP for a test (which is entirely possible!) I put it to his last GP that he ought to be tested.  He looked at Dad's blood results and purely because he was not anemic said he wasn't a coeliac. (This was the same GP who said Dad didn't have dementia, when months before one of his colleagues suspected it and told me Dad must be diagnosed).  Hopefully as the awareness of Coeliac Disease spreads among the general public, people will be able to advocate for themselves.  It is hard because in the UK the NHS is very stretched, but the fallout from not being diagnosed in a timely fashion will only cost the NHS more money. Interestingly, a complete aside, I met someone recently whose son was diagnosed (I think she said he was 8).  At a recent birthday party with 8 guests, 4 boys out of the 8 had received diagnosis of Coeliac Disease, which is an astounding statistic  As far as I know, though, they had all had obvious gastric symptoms leading to their NHS diagnosis.  In my own case I had  acute onset anxiety, hypnopompic hallucinations (vivid hallucinations upon waking),  odd liver function, anxiety, headaches, ulcers and low iron but it wasn't until the gastric symptoms hit me that a GP thought to do coeliac testing, and my numbers were through the roof.  As @trents says, by the grace of God I was diagnosed, and the diet has pretty much dealt with most of those symptoms.  I have much to be grateful for. Cristiana
    • knitty kitty
      My journey is it gluten or fiber?

      By knitty kitty · Posted

      @xxnonamexx, There's labeling on those Trubar gluten free high fiber protein bars that say: "Manufactured in a facility that also processes peanuts, milk, soy, fish, WHEAT, sesame, and other tree nuts." You may want to avoid products made in shared facilities.   If you are trying to add more fiber to your diet to ease constipation, considering eating more leafy green vegetables and cruciferous vegetables.  Not only are these high in fiber, they also are good sources of magnesium.  Many newly diagnosed are low in magnesium and B vitamins and suffer with constipation.  Thiamine Vitamin B1 and magnesium work together.  Thiamine in the form Benfotiamine has been shown to improve intestinal health.  Thiamine and magnesium are important to gastrointestinal health and function.  
    • trents
      Issues before diagnosis

      By trents · Posted

      Welcome to celiac.com @sha1091a! Your experience is a very common one. Celiac disease is one the most underdiagnosed and misdiagnosed medical conditions out there. The reasons are numerous. One key one is that its symptoms mimic so many other diseases. Another is ignorance on the part of the medical community with regard to the range of symptoms that celiac disease can produce. Clinicians often are only looking for classic GI symptoms and are unaware of the many other subsystems in the body that can be damaged before classic GI symptoms manifest, if ever they do. Many celiacs are of the "silent" variety and have few if any GI symptoms while all along, damage is being done to their bodies. In my case, the original symptoms were elevated liver enzymes which I endured for 13 years before I was diagnosed with celiac disease. By the grace of God my liver was not destroyed. It is common for the onset of the disease to happen 10 years before you ever get a diagnosis. Thankfully, that is slowly changing as there has developed more awareness on the part of both the medical community and the public in the past 20 years or so. Blessings!
    • knitty kitty
      Dizziness after eating green beans?

      By knitty kitty · Posted

      @EndlessSummer, You said you had an allergy to trees.  People with Birch Allergy can react to green beans (in the legume family) and other vegetables, as well as some fruits.  Look into Oral Allergy Syndrome which can occur at a higher rate in Celiac Disease.   Switching to a low histamine diet for a while can give your body time to rid itself of the extra histamine the body makes with Celiac disease and histamine consumed in the diet.   Vitamin C and the eight B vitamins are needed to help the body clear histamine.   Have you been checked for nutritional deficiencies?
    • sha1091a
      Issues before diagnosis

      By sha1091a · Posted

      I found out the age of 68 that I am a celiac. When I was 16, I had my gallbladder removed when I was 24 I was put on a medication because I was told I had fibromyalgia.   going to Doctor’s over many years, not one of them thought to check me out for celiac disease. I am aware that it only started being tested by bloodwork I believe in the late 90s, but still I’m kind of confused why my gallbladder my joint pain flatulent that I complained of constantly was totally ignored. Is it not something that is taught to our medical system? It wasn’t a Doctor Who asked for the test to be done. I asked for it because of something I had read and my test came back positive. My number was quite high.Are there other people out here that had this kind of problems and they were ignored? 
×
×
  • 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.