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

Dont get mad, but whats the big deal about 20 PPM?


Washingtonmama

Recommended Posts

Washingtonmama Contributor

I know what it means, and some people are SEVERELY sensitive to it. I have almost no symptoms when I get a tiny bit of gluten. I get gunk running down the back of my throat for a day or two, maybe diarrhea if I eat a bite of something with wheat. What kind of damage does a fraction of gluten do? How severe is it? How long does it last? Do I even need to avoid fractions of gluten? I was just diagnosed last week, so Im still learning. 


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

Just focus on avoiding gluten.  You will know soon enough if you are super sensitive or not.  There is no way to tell, unless you get scoped all the time or you have DH.  Celiac symptoms can change. I was just anemic when diagnosed.  I probably had a few other symptoms that I chalked up to menopause (like anxiety or irritability --- and who would not with 30 day periods!), yet I had moderate to severe patches of villi damage.   Now, I get the classic gut symptoms when exposed to gluten.  

Unfortunately, researchers really don't want to spend anymore time studying this.  They probably  needed a cut-off for the food manufacturers and to implement current laws and regulations.  But we all know that celiac disease is not simple and it's not "one size fits all".  I can tell you that some members eat out  and consume lots of gluten-free processed foods that are not even labeled gluten-free.  They have had follow-up biopsies that have shown no villi damage.  Others are on the gluten-free diet and still have damage.  The point is no one knows for sure.  You just have to figure it out in your own.

Just keep moving forward!  

 

Ennis-TX Grand Master

Celiac is a Autoimmune disease, your body reacts in a similar fashion to the gluten proteins as it does to a germ. A tiny bit will trigger the immune response and your body will release the antibodies to try to attack it damaging your body in the process more or less as a mistaken collateral damage. The antibodies will remain high for weeks afterwards slowly stepping down in response just to make sure they killed it.     NOW in relation to the PPM in the US 20ppm is what is the government required maximum a food can have to be labeled gluten free. Some other countries have it lower, in Europe many have a 5 or 10ppm rule and Australia was pushing for a 0ppm rule.  

As for how you react we are all different, and other things come into the equations for how much of the actual gluten gets to your system. When in very minute amounts below 20ppm and a bit higher the gluten proteins might get damaged, or blocked from being absorbed during food prep, and digestion processes if your lucky, or your body will fight them in the background without having to go completely crazy.  

For me it is really odd, some times I think I get a bit of gluten, and notice a tiny bit of brain fog and less feeling in my hands and feet. Maybe a bit looser stools in very small amounts (Been using a product I sent to a lab for testing at 6ppm and notice these when I consume 1/4 cup of it)  I know other times I have gotten pretty sick from a crumbs, complete fog and dazed from inhaling flour walking through a bakery. 

Now last time I got a full blown gluten attack was from eating out, I had a tiny bit of pulled chicken over salad and steamed veggies, I later learned the chicken had been dredged in four, and they did something a bit special for me for the veggies freshly steaming them since the ones they had already done were butter coated.....well they fresh steamed them over pasta water.   Felt it coming before it hit and rushed home got in the door and, loosing complete motor control dropped to the floor, convulsing in pain and vomiting for hours in my door way. I had a friend who was watching over me, they actually thought I was dead at a few points saying I turned completely white. I wear a fitness monitor and my heart rate for a hour or so dropped to the 32-36 range.  After 7-8 hours I was able to get to the couch and sleep the rest of it off with D all the next day. I then called the restaurant and learned about chicken and the veggies......The manager apologized and it seems the issues was a mis communication and misunderstanding with the chef and the waiter when I told them about my list of allergies and celiac disease. They were not to detailed on it and I have never been back to Red Hot & Blues since.

I do not think you should worry much, just stick to washed naturally gluten-free whole veggies, fruits, meats. And Certified gluten-free foods and you should be just fine. Some naturally gluten free foods in cans and frozen can be safe from certain companies, NOTE if the company does a sauced version or other things that contain gluten think twice.  Always read ingredients and allergen warnings on anything you buy.

GFinDC Veteran

20 PPM is what the FDA set as an upper limit for labeling foods gluten-free in the USA.  But the research they based it on had some participants drop out due to symptoms at that level.  So some people can and do react to lower levels than 20 PPM.

Your immune system "sees" microscopic germs and attacks them.  You can't see those germs with your naked eye.  But your immune system detects them and reacts to kill them.

Washingtonmama Contributor

Ok I understand now. You eat a tiny particle of gluten, and your body, in trying to protect itself, actually attacks itself. It keeps attacking and doing damage for a few weeks, even though you have no idea what's going on. Is that correct? Thanks for your help everyone! 

Washingtonmama Contributor

Ennis, all I can say is OMG to what happened to you at the restaurant! Geeze! Can you actually die from that kind of reaction? Is there anything they can do at the hospital to help? 

Ennis-TX Grand Master
30 minutes ago, Washingtonmama said:

Ennis, all I can say is OMG to what happened to you at the restaurant! Geeze! Can you actually die from that kind of reaction? Is there anything they can do at the hospital to help? 

Many of us have reactions that get us put in the ER, not much they co do for it, not quite a gluten ebipen yet lol. Plus side I just heard recent news of a new vaccine that turns off the T cells for the gluten antibodies or something like that that is in clinical trials.   I decided to wait it out and just put up with it. at that time I had no insurance so hospital was not a option and nothing they could have done to my knowledge.  

You see the reason why some of us are overly paranoid, if you get that kind of reaction a few times your scared and overly cautious about everything. Washing your hands, not eating out, using expensive test kits, always having emergency meals laid out, and covering your food prep surfaces with freezer paper. Heck I even bring plastic utensils, cups, and bowls when I eat outside my house. Scariest thing in the world is having your own mind and body not do what you want. lol I fear how I would react to a prank if someone did something with gluten or flour on purpose.


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



Celiac.com Sponsor (A8-M):



Jmg Mentor
1 hour ago, Washingtonmama said:

Ok I understand now. You eat a tiny particle of gluten, and your body, in trying to protect itself, actually attacks itself. It keeps attacking and doing damage for a few weeks, even though you have no idea what's going on. Is that correct? Thanks for your help everyone! 

Pretty much. It gets complicated because for some of us it's not just a digestive issue. Gluten messes me with in many ways, of which the digestive is very much a minor player. The neurological aspects are worse for me and they take a lot longer to go. I get depression, brain fog, anxiety, eye issues, nerve stuff etc. I get back pain, chest pain, skin rashes. It's bizarre really and not easy to explain to someone who hasnt experienced it. I'm sure lots of people think I'm nuts. :)

Two links for you which would do a better job than I could. Check out gluten man Open Original Shared Link and see what a range of symptoms can be. For some the tiniest exposure can trigger any one or more combination. 

There's a good article here which shows some of the theories how gluten in the gut can affect the brain: Open Original Shared Link

Hope these of interest :)

 

RMJ Mentor

Antibody reactions to a given amount of antigen (gluten) vary greatly from person to person.  Even if you're trying to create antibodies in very, very inbred animals that are almost identical genetically, the amount of antibodies they will create varies a lot.  If you're lucky you won't be in the super sensitive geoup.

  • 3 weeks later...
pdm1981 Collaborator

You would think that there is enough people out there, people with celiac disease, that we'd be able to push for a better standard than 20ppm. The problem is the FDA. Too much lobbying involved. It's no different than the fight people are having with Monsanto. I hear that there are several medications that are showing promise in Canada who I think also has a better standard than us.(not positive about that though)

Gemini Experienced
On 4/24/2017 at 7:28 AM, pdm1981 said:

You would think that there is enough people out there, people with celiac disease, that we'd be able to push for a better standard than 20ppm. The problem is the FDA. Too much lobbying involved. It's no different than the fight people are having with Monsanto. I hear that there are several medications that are showing promise in Canada who I think also has a better standard than us.(not positive about that though)

The reason they set the limit at 20ppms is that through scientific study, they have proven that the vast majority of people with Celiac Disease do not have an autoimmune reaction to amounts below that......it is a safe limit for most.  Also, just because that limit is set at 20ppms, does not mean that gluten-free products contain that amount of gluten.  Testing for lower levels becomes more expensive with each increment down closer to 0-5ppms, which translates into higher priced products. Unless you eat a lot of processed gluten-free food, which can have a cumulative affect for some, most people do well with the 20ppm limit. 

 

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. - trents replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?

    2. - BlessedinBoston replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?

    3. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      14

      My only proof

    4. - Jmartes71 replied to Jmartes71's topic in Related Issues & Disorders
      14

      My only proof

    5. - marion wheaton posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Are Lindt chocolate balls gluten free?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,407
    • Most Online (within 30 mins)
      7,748

    H2HPizzaWagon
    Newest Member
    H2HPizzaWagon
    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

    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
    • marion wheaton
      Wondering if anyone knows whether Lindt chocolate balls are gluten free. The Lindt Canadian website says yes but the Lindt USA website says no. The information is a bit confusing.
×
×
  • 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.