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

Papa Johns Pizza, Vitamin A, DH...


Bob Jones

Recommended Posts

Bob Jones Newbie

I'm a self diagnosed celiac in that I had for several years the common traits of celiac disease(I had no idea about the disease before). It was most likely entirely due taking accutane but showed up gradually over a few years.

In any case once I started cutting out the gluten I stopped getting sick(mainly the s$#&s and stomach aches). It seems any time I eat gluten I can have a rather quick reaction and usually know I've made a mistake.

I've noticed though that I never had much problem with pappa johns pizza. I've been rather gluten free(for the most part) for about 1/2 a year but I'm pretty sure I've had some stuff that was contaminated.

This weekend I ate 2 pizzas 1 per day and had very little if any reaction. This is very surprising to me since even a something mild as a cracker can sometimes send me running. I did drink A LOT of water when I hate the pizzas(about 4 bottles over a 30min period) and I took some vitamins while I was eating the pizza. (I repeated this the next day to see if it was going to cause any problems and it didn't seem to).

From my understanding I should have definitely had some reaction. It is possible I had a mild reaction but wasn't severe enough to cause problems. Also, the week before I was eating nothing but potatoes and apples because I ran out of gluten free products.

While I can't be 100% sure I'm a celiac I would bet the chance is 95%+. All the symptoms are there to a 'T' and obviously removing the gluten seems to solve the problem. What's weird is that sometimes having gluten doesn't give a reaction and sometimes it does.

So I have a few questions:

1. Is there anything "special" about the bread in PJ's pizza that may make it less likely to cause symptoms?

2. What is the normal digestive reaction time when indigestion gluten to cause the intestines to go into shock(the runs!). It almost seems like the intestines are trying to flush out all the material as a normal reaction. (It's almost more like water coming out than anything else).

3. Suppose that for some odd reason I am not having the obvious reaction to PJ's as others. Am I doing harm to my gut if I eat the pizza? Obvious answer is yes but can I splurge every once in a while or am I doing more harm than good. (Gets old eating the same crap because of the limited gluten free foods around)

I'm just wondering if I don't have a physically noticeable reaction if something that is just as serious could still be happening. i.e., the destruction of the intestines just as much as any other case.

4. Has anyone noticed if certain things help reduce the symptoms when eating gluten such as certain vitamins, fruits, etc or if certain "forms" of gluten seem to have less of a reaction?

Since it seems that accutane is almost surely created celiac in most people that use it and it is a vitamin A derivative maybe there is a connection between gluten and vitamin A.

Just curious!!!!


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



Celiac.com Sponsor (A8-M):



rosetapper23 Explorer

Wow--lots of questions! I may not have the "answers," but I'm going to guess on a couple of them.

I read not long ago that sourdough bread has a component in it that causes some people not to have a reaction to gluten, so maybe Papa John's uses a sourdough-type crust (??). Just hazarding a guess here....

However, I also really missed pizza, so there was a period of time when I ate it once a month...and I didn't seem to have any reaction to it. That said, after about six months, my ferritin level fell and could NOT be raised no matter how much oral iron I took, so I had to go on iron infusions for years. Apparently, even though I wasn't suffering from any symptoms, damage was still being done. Nowadays, even the slight gluten contamination causes illness and horrible nutritional deficiencies. I got glutened in April 2010, and I'm still suffering the effects of that mistake.

Regarding Vitamin A, there was a recent study that showed that Vitamin A is highly inflammatory for people with celiac disease. I've never been able to take Vitamin A because I'd get immediately ill, and when dermatologists (don't get me started on those idiots!) thought I had a severe case of acne rather than Dermatitis Herpetiformis (DH), they prescribed Retin-A, which completely burned the heck out of my skin. Took years to get rid of the scars.

Are you sure that what you have/had is actually acne? It could be that you suffered from DH. Also, it's possible that a number of celiacs, not knowing they had DH rather than acne, were placed on Accutane....so it might not have been the Accutane that triggered celiac but, rather, a misdiagnosis from the very beginning.

psawyer Proficient

Are you sure that what you have/had is actually acne? It could be that you suffered from DH. Also, it's possible that a number of celiacs, not knowing they had DH rather than acne, were placed on Accutane....so it might not have been the Accutane that triggered celiac but, rather, a misdiagnosis from the very beginning.

This is a very important observation. A correlation between two events does not mean one causes the other.

sreese68 Enthusiast

Are you sure that what you have/had is actually acne? It could be that you suffered from DH. Also, it's possible that a number of celiacs, not knowing they had DH rather than acne, were placed on Accutane....so it might not have been the Accutane that triggered celiac but, rather, a misdiagnosis from the very beginning.

Slightly off topic, but

Lori2 Contributor

Regarding Vitamin A, there was a recent study that showed that Vitamin A is highly inflammatory for people with celiac disease. I've never been able to take Vitamin A because I'd get immediately ill, and when dermatologists (don't get me started on those idiots!) thought I had a severe case of acne rather than Dermatitis Herpetiformis (DH), they prescribed Retin-A, which completely burned the heck out of my skin. Took years to get rid of the scars.

Could you give us a reference on the Vitamin A being inflammatory. I would like to study this a bit.

  • 3 weeks later...
newyorkyankz Newbie

Why not have the test to be 100 % sure you have it?

  • 6 months later...
AHopewell Newbie

I'm a self diagnosed celiac in that I had for several years the common traits of celiac disease(I had no idea about the disease before). It was most likely entirely due taking accutane but showed up gradually over a few years.

In any case once I started cutting out the gluten I stopped getting sick(mainly the s$#&s and stomach aches). It seems any time I eat gluten I can have a rather quick reaction and usually know I've made a mistake.

I've noticed though that I never had much problem with pappa johns pizza. I've been rather gluten free(for the most part) for about 1/2 a year but I'm pretty sure I've had some stuff that was contaminated.

This weekend I ate 2 pizzas 1 per day and had very little if any reaction. This is very surprising to me since even a something mild as a cracker can sometimes send me running. I did drink A LOT of water when I hate the pizzas(about 4 bottles over a 30min period) and I took some vitamins while I was eating the pizza. (I repeated this the next day to see if it was going to cause any problems and it didn't seem to).

From my understanding I should have definitely had some reaction. It is possible I had a mild reaction but wasn't severe enough to cause problems. Also, the week before I was eating nothing but potatoes and apples because I ran out of gluten free products.

While I can't be 100% sure I'm a celiac I would bet the chance is 95%+. All the symptoms are there to a 'T' and obviously removing the gluten seems to solve the problem. What's weird is that sometimes having gluten doesn't give a reaction and sometimes it does.

I have figured out the same exact thing. For some reason Papa John's pizza does not affect me like others when I am brave enough to try it. Wish we knew the WHYs.


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



Celiac.com Sponsor (A8-M):



  • 3 weeks later...
Ryniev Apprentice

I have figured out the same exact thing. For some reason Papa John's pizza does not affect me like others when I am brave enough to try it. Wish we knew the WHYs.

I always tried to avoid Papa John's in particular when I still ate gluten because it hurt my stomach worse than anything. My stomach would swell up to three times it's normal size and along with the diahrea, cramps and never-ending gas!

I know I'm not your mother (or your doctor) but I'm throwing this out there as a life lesson. Five years ago I suspected I had celiac disease. I finally got a dr. to do a blood test and it was negative. Went back to eating gluten gradually and for a while it was okay.

It eventually caught up to me in spades. I got to the point where if they told me all I could eat for the rest of my life was bananas to feel better I would do it. At this point, I don't even mess with "trying just a little". Please don't take this as a lecture, I just truly want to spare people what I've been through.

squirmingitch Veteran

I've noticed though that I never had much problem with pappa johns pizza. I've been rather gluten free(for the most part) for about 1/2 a year but I'm pretty sure I've had some stuff that was contaminated.

This weekend I ate 2 pizzas 1 per day and had very little if any reaction. This is very surprising to me since even a something mild as a cracker can sometimes send me running. I did drink A LOT of water when I hate the pizzas(about 4 bottles over a 30min period) and I took some vitamins while I was eating the pizza. (I repeated this the next day to see if it was going to cause any problems and it didn't seem to).

From my understanding I should have definitely had some reaction. It is possible I had a mild reaction but wasn't severe enough to cause problems. Also, the week before I was eating nothing but potatoes and apples because I ran out of gluten free products.

So I have a few questions:

1. Is there anything "special" about the bread in PJ's pizza that may make it less likely to cause symptoms?

2. What is the normal digestive reaction time when indigestion gluten to cause the intestines to go into shock(the runs!). It almost seems like the intestines are trying to flush out all the material as a normal reaction. (It's almost more like water coming out than anything else).

3. Suppose that for some odd reason I am not having the obvious reaction to PJ's as others. Am I doing harm to my gut if I eat the pizza? Obvious answer is yes but can I splurge every once in a while or am I doing more harm than good. (Gets old eating the same crap because of the limited gluten free foods around)

I'm just wondering if I don't have a physically noticeable reaction if something that is just as serious could still be happening. i.e., the destruction of the intestines just as much as any other case.

4. Has anyone noticed if certain things help reduce the symptoms when eating gluten such as certain vitamins, fruits, etc or if certain "forms" of gluten seem to have less of a reaction?

Do you believe in magic? I don't.

sa1937 Community Regular

The OP only made one post on the forum on July 9...so it's doubtful that he'll even see these last responses.

For anyone else reading...it is NOT okay to eat Papa John's pizza on a gluten-free diet!!!

squirmingitch Veteran

Thanks for pointing that out Sylvia. Makes one wonder if someone was pulling a prank doesn't it?

sa1937 Community Regular

Thanks for pointing that out Sylvia. Makes one wonder if someone was pulling a prank doesn't it?

It sure does or they simply don't want to deal with the answers they get. We also have a number of people come on and post once or twice and then simply disappear never to be heard from again.

Ryniev Apprentice

It sure does or they simply don't want to deal with the answers they get. We also have a number of people come on and post once or twice and then simply disappear never to be heard from again.

I didn't even look at the date, I just saw the topic and thought, "wow! Papa John's doesn't make someone sick". :blink: I was one of those people that posted 5 or 6 times several years ago and left. Some of us come back. When my blood test came back negative several years ago, I didn't think I belonged. Come to find out, I do.

sa1937 Community Regular

I didn't even look at the date, I just saw the topic and thought, "wow! Papa John's doesn't make someone sick". :blink: I was one of those people that posted 5 or 6 times several years ago and left. Some of us come back. When my blood test came back negative several years ago, I didn't think I belonged. Come to find out, I do.

We can dream, can't we! tongue.gif Hopefully everyone reads past the first post when a title like that catches their attention!!! If something sounds too good to be true, it usually is.

And welcome back!!! Now you know that you belong here with us! smile.gif

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,953
    • Most Online (within 30 mins)
      7,748

    ramonaja
    Newest Member
    ramonaja
    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.