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

California Pizza Kitchen


pshifrin

Recommended Posts

pshifrin Apprentice

My wife had a 20% off coupon for CPK so we decided to check out their new gluten-free offerings at the Scarsdale, NY location. Yes I know it's a chain and it's filled with Gluten. I'm intolerant, not Celiac so I was willing to take a chance. Their gluten-free menu came out just a few weeks ago (it's integrated into the regular menu so you don't have to ask for a separate one). It includes a short list of apps, salads, one entree and of course Pizza. All the pizza's can be made gluten-free except two. I ordered the Hawaiian BBQ Chicken Pizza.

Pizza came out, i bit into it and got very worried... it was too good. It was soft a chewy in all the right places and firm on the bottom. I stopped the waitress and verified it was gluten-free, she said yes. I visually compared my pizza to my wife's (she got the whole wheat) and our son's (he got a kid's regular). My pizza crust definitely looked different. I had my wife do a taste test, she thought it was gluten-free. See the problem is the bbq chicken pizza has such an overwhelming flavor (in a good way) that it was hard to taste just the crust. I looked around at other people's pizza, mine didn't look the same.

Here's the bottom line, except for Mozzerrelli's in NYC, this was BY FAR the best gluten-free pizza I've ever tasted. Better than Unos, Pizza Fusion, Mellow Mushroom, any Still Riding or French Meadow i've had in many local pizza places.

I asked the mgr to stop by and chat. Quizzed her on their gluten-free operations. She said they keep the dough separate, prep and cook the pizza on a clean pan and / or aluminum foil, change gloves while prepping it and cook it "not close to the other pizzas." For an intolerant person like myself, I found this completely adequate. FYI, she said they sell about 4 a day on average.

If you used to enjoy CPK and hopefully your local outlet follows the correct procedures, run don't walk. Speaking of running, I'm going to have to burn off some major calories after my lunch at Open Original Shared Link and dinner at Open Original Shared Link.


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



Celiac.com Sponsor (A8-M):



tea-and-crumpets Explorer

That's great that they are paying attention to the CC risks. When they were testing the menu in my area I was told that they had no consideration for CC, used the same pans, all that. It's great to have another option. Thanks for the update.

Juliebove Rising Star

Thanks! I just looked and sadly there are eggs in the crust. So won't work for me.

brendygirl Community Regular

I'm salivating just thinking about it! There's a CPK down the street. I'll be on my way for dinner tonight!

cyberprof Enthusiast

Any celiacs or sensitive people tried this? This might be good for my son, who's less sensitve than I am....

JSWM Newbie

I was just coming to this forum to post about CPK. I went there today. . . a fav of mine! I was so excited that they are so gluten-free friendly! They also have a new gluten-free appetizer, the white corn guacomole that is AWESOME!!! one of the only gluten-free appetizers and great! I will def be going there more often!

melikamaui Explorer

CPK was a staple of ours before everyone was diagnosed (me and both of my children). Their BBQ chicken pizza (sans chicken, I sub avocado instead) was my absolute favorite food of all time. I was SO excited when I found out they were starting a gluten-free menu! Before we went I called our local restaurant and talked to the manager to make sure they were uber-careful about CC. Turns out the managers mother has celiac disease! He answered everything to my satisfaction and we went for lunch the next day. Right when we arrived I asked to see the manager. He came over to our table as I was wiping it down with my wipes from home (too much gluten in a pizza place for me NOT to do that) and said how excited he was that we were there. He said he would personally watch the chefs make our pizzas. And he did! He came over as they were cooking and walked me step-by-step through everything they did. Though I liked the pizza, it tasted like pretty typical gluten-free crust to me. Not what I was hoping for, but it was good. After dinner he gave me his card and told me to email him that night in the hopes that we were all healthy and there were no signs of contamination. We waited about 8 hours, figured out we were all healthy and then emailed him. He was very happy and sent a copy of my email to corporate.

We are THRILLED with the attention CPK is giving this issue, and have been back once more since then. Big thumbs up from my family! :D


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



Celiac.com Sponsor (A8-M):



modiddly16 Enthusiast

I've actually heard quite recently that the CPK's gluten free menu is misleading...I Saw this article from the Gluten Free Girl blog that I follow.

Open Original Shared Link

Apparently their Director of Culinary Devlopment has also said that CPK's Gluten Free pizza is NOT meant for people with celiac disease, but for people who choose not to eat gluten, as they cannot guarantee that it's gluten free.

The article is worth reading before you go eat there, then the decision is yours!

Archived

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

  • 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. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      8

      My only proof

    2. - Wheatwacked replied to Jmartes71's topic in Coping with Celiac Disease
      8

      Related issues

    3. - NanceK replied to Jmartes71's topic in Related Issues & Disorders
      8

      My only proof

    4. - Wheatwacked replied to Scatterbrain's topic in Sports and Fitness
      4

      Feel like I’m starting over

    5. - Scott Adams replied to Kirita's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      Recovery from gluten challenge


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,290
    • Most Online (within 30 mins)
      7,748

    Joycemarie
    Newest Member
    Joycemarie
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • knitty kitty
      @NanceK, I do have Hypersensitivity Type Four reaction to Sulfa drugs, a sulfa allergy.  Benfotiamine and other forms of Thiamine do not bother me at all.  There's sulfur in all kinds of Thiamine, yet our bodies must have it as an essential nutrient to make life sustaining enzymes.  The sulfur in thiamine is in a ring which does not trigger sulfa allergy like sulfites in a chain found in pharmaceuticals.  Doctors are not given sufficient education in nutrition (nor chemistry in this case).  I studied Nutrition before earning a degree in Microbiology.  I wanted to know what vitamins were doing inside the body.   Thiamine is safe and nontoxic even in high doses.   Not feeling well after starting Benfotiamine is normal.  It's called the "thiamine paradox" and is equivalent to an engine backfiring if it's not been cranked up for a while.  Mine went away in about three days.  I took a B Complex, magnesium and added molybdenum for a few weeks. It's important to add a B Complex with all eight essential B vitamins. Supplementing just one B vitamin can cause lows in some of the others and result in feeling worse, too.  Celiac Disease causes malabsorption of all the B vitamins, not just thiamine.  You need all eight.  Thiamine forms including Benfotiamine interact with each of the other B vitamins in some way.  It's important to add a magnesium glycinate or chelate supplement as well.  Forms of Thiamine including Benfotiamine need magnesium to make those life sustaining enzymes.  (Don't use magnesium oxide.  It's not absorbed well.  It pulls water into the intestines and is used to relieve constipation.)   Molybdenum is a trace mineral that helps the body utilize forms of Thiamine.   Molybdenum supplements are available over the counter.  It's not unusual to be low in molybdenum if low in thiamine.   I do hope you will add the necessary supplements and try Benfotiamine again. Science-y Explanation of Thiamine Paradox: https://hormonesmatter.com/paradoxical-reactions-with-ttfd-the-glutathione-connection/#google_vignette
    • Wheatwacked
      Your goal is not to be a good puppet, there is no gain in that. You might want to restart the ones that helped.  It sounds more like you are suffering from malnutrition.  Gluten free foods are not fortified with things like Thiamine (B1), vitamin D, Iodine, B1,2,3,5,6 and 12 as non-gluten free products are required to be. There is a Catch-22 here.  Malnutrition can cause SIBO, and SIBO can worsen malnutrition. Another possibility is side effects from any medication that are taking.  I was on Metformin 3 months before it turned me into a zombi.  I had crippling side effects from most of the BP meds tried on me, and Losartan has many of the side effects on me from my pre gluten free days. Because you have been gluten free, you can test and talk until you are blue in the face but all of your tests will be negative.  Without gluten, you will not create the antigen against gluten, no antigens to gluten, so no small intestine damage from the antigens.  You will need to do a gluten challange to test positive if you need an official diagnosis, and even then, no guaranty: 10 g of gluten per day for 6 weeks! Then a full panel of Celiac tests and biopsy. At a minimum consider vitamin D, Liquid Iodine (unless you have dermatitis herpetiformis and iodine exasperates the rash), and Liquid Geritol. Push for vitamin D testing and a consult with a nutritionist experienced with Celiack Disease.  Most blood tests don't indicate nutritional deficiencies.  Your thyroid tests can be perfect, yet not indicate iodine deficiency for example.  Thiamine   test fine, but not pick up on beriberi.  Vegans are often B12 deficient because meat, fish, poultry, eggs, and dairy are the primary souces of B12. Here is what I take daily.  10,000 IU vitamin D3 750 mg g a b a [   ] 200 mg CoQ10 [   ] 100 mg DHEA [   ] 250 mg thiamine B1 [   ] 100 mg of B2 [   ] 500 mg B5 pantothenic acid [   ] 100 mg B6 [   ] 1000 micrograms B12 n [   ] 500 mg vitamin c [   ] 500 mg taurine [   ] 200 mg selenium   
    • NanceK
      Hi…Just a note that if you have an allergy to sulfa it’s best not to take Benfotiamine. I bought a bottle and tried one without looking into it first and didn’t feel well.  I checked with my pharmacist and he said not to take it with a known sulfa allergy. I was really bummed because I thought it would help my energy level, but I was thankful I was given this info before taking more of it. 
    • Wheatwacked
      Hello @Scatterbrain, Are you getting enough vitamins and minerals.  Gluten free food is not fortified so you may be starting to run low on B vitamins and vitamin D.   By the way you should get your mom checked for celiac disease.  You got it from your mom or dad.  Some studies show that following a gluten-free diet can stabilize or improve symptoms of dementia.  I know that for the 63 years I was eating gluten I got dumber and dumber until I started GFD and vitamin replenishment and it began to reverse.  Thiamine can get used up in a week or two.  Symptoms can come and go with daily diet.  Symptoms of beriberi due to Thiamine deficiency.   Difficulty walking. Loss of feeling (sensation) in hands and feet. Loss of muscle function or paralysis of the lower legs. Mental confusion. Pain. Speech difficulties. Strange eye movements (nystagmus) Tingling. Any change in medications? Last March I had corotid artery surgery (90 % blockage), and I started taking Losartan for blood pressure, added to the Clonidine I was taking already.  I was not recovering well and many of my pre gluten free symptoms were back  I was getting worse.  At first I thought it was caused a reaction to the anesthesia from the surgery, but that should have improved after two weeks.  Doctor thought I was just being a wimp. After three months I talked to my doctor about a break from the Losartan to see if it was causing it. It had not made any difference in my bp.  Except for clonindine, all of the previous bp meds tried had not worked to lower bp and had crippling side effects. One, I could not stand up straight; one wobbly knees, another spayed feet.  Inguinal hernia from the Lisinopril cough.  Had I contiued on those, I was destined for a wheelchair or walker. She said the symptoms were not from Losartan so I continued taking it.  Two weeks later I did not have the strength in hips and thighs to get up from sitting on the floor (Help, I can't get up😨).  I stopped AMA (not recommended).  Without the Losartan, a) bp did not change, after the 72 hour withdrawal from Losartanon, on clonidine only and b) symptoms started going away.  Improvement started in 72 hours.  After six weeks they were gone and I am getting better.  
    • Scott Adams
      Hopefully the food she eats away from home, especially at school, is 100% gluten-free. If you haven't checked in with the school directly about this, it might be worth a planned visit with their staff to make sure her food is safe.
×
×
  • 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.