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. - marlene333 replied to Grace Good's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Bee balm lipbalm not gluten free

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

      Related issues

    3. - Scott Adams replied to catsrlife's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      Patiently Waiting to See Results

    4. - catsrlife replied to catsrlife's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      Patiently Waiting to See Results

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

      Related issues


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,263
    • Most Online (within 30 mins)
      7,748

    Elyn Joy
    Newest Member
    Elyn Joy
    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

    • marlene333
      To play it safe, use Vasoline Lip Therapy. No questions as to it containing gluten.
    • Mari
      jmartes, Thank you for sharing  more information with us. Most of us Celiacs whose problems do not clear up with in a few years have to decide what to do next. We can keep seeing DR.s and hope that we will get some  medication or advice that will improve our health. Or we can go looking for other ways to improve our health. Usually Celiac Disease is not a killer disease, it is a disabling disease as  you have found out. You have time to find some ways to help you recover. Stay on your gluten-free diet and be more careful in avoiding cross contamination . KnittyKitty  and others here can give you advice about avoiding some foods that can give you the gluten auto immune reaction and advice about vitamins and supplement that help celiacs. You may need to take higher doses of Vit. B12  and D3.  About 20 years before a Dr. suggested I might have Celiac disease I had health problems that all other Dr said they could not identify or treat. I was very opposed to alternative providers and treatments. So many people were getting help from a local healer I decided to try that out. It was a little helpful but then, because I had a good education in medical laboraties she gave me a book  to read and what did I think. With great skeptism I started reading and before I was half way through it I began using the methods outlined in the book. Using those herbs and supplements I went from hardly able to work to being able to work almost fulltime. I still use that program. But because I had undiagnosed celiac disease by 10 years later some  of my problems returned and I started to loose weight.    So how does a person find a program that will benefit them? Among the programs you can find online there are many that are snake oil scams and some that will be beneficial. by asking around, as I did. Is there an ND in your area? Do they reccomend that person? If you would like to read about the program I use go to www.drclark.net   
    • Scott Adams
      It's unfortunate that they won't work with you on this, but in the end sometimes we have to take charge of our own health--which is exactly what happened to me. I did finally get the tests done, but only after years of going down various rabbit holes and suffering. Just quitting gluten may be the best path for you at this point.
    • catsrlife
      My doctor didn't take the time to listen to anything. I don't even think she knows what it means. She is more concerned about my blood pressure that is caused by her presence than anything else and just wants to push pills at me. The so-called dermatologist wouldn't do a skin test. she prescribed all of these silly antihistamine skin meds. This lady didn't even know what she was talking about and said "they never turn out as celiac, they usually just say it's dermatitis so here's your meds," just like my regular quack. I'm trying to change insurance companies at the moment and that has been a battle because of red tape, wrong turns, and workers having wrong phone numbers. What a joke! The allergy blood days say I have a wheat allergy of .31. Hopefully it's just that and until I find a decent doctor and dermatologist, I'll just lay off the wheat anyway, since it gives me asthma, high blood sugar, and joint pain. So frustrated at this point. The rash on my back of arms/elbows is mostly gone. Both calves and chest have started up. smh. It comes and goes. It fades faster now, though, although my forearms still produce one or two bumps on each side. The itching has calmed down a lot except for the bump area. I have dry skin to begin with so anything affecting it just makes it crazy. i'm never going to eat wheat again. I don't care if they need it to produce results or if it is just an intolerance, allergy, or celiac. It gives me hell.
    • Jmartes71
      I had the test done by one of the specialist through second pcp I had only a few months because he was saying I wasn't.Even though Im positive HLA-DQ2 .My celiac is down played.I am with new pcp, seeing another girl doctor who wants to do another breathe test next month though Im positive sibo this year.I have high blood pressure not sure if its pain from sciatica or sibo, ibs or hidden gluten. Im in disability limbo and I should have never been a bus driver because im still suffering and trying to heal with zero income except for my husband. This isnt fare that my health is dictating my living and having ti beg for being revalidation of my disregarded celiac disease. Its an emotional roller coaster I don't want to be on and the medical made it worse.New pcp new gi, exhausted, tired and really fed up. GI doctor NOT girl..
×
×
  • 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.