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

Rice Krispies


es2443

Recommended Posts

Wheatfreedude Apprentice

I wish I would have read this post before I ate RK treats this past Saturday night.

~Wheatfreedude~

(Now "Ricekrispyfreedude too) :angry:

  • 1 month later...

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



Celiac.com Sponsor (A8-M):



pghmamacita Newbie

Ok, I am new to this with my son being diagnosed this year, but I like to read up on things that will make big changes in my life...and if you have celiac disease even a speck of gluten can cause problems. You may not feel anything physically, but inside it is going to cause complications. Do you people read up on a serious disease you were diagnosed with????? Seriously, trace amounts of gluten add up and I am sorry but I am not putting my child at risk by allowing him something that contains the word malt in it. They are not safe, and if you truly care about yourself and you have celiac disease you will read up on what it does to your body when you consume gluten.

Here is some great advice....when in doubt, do without!!!!

psawyer Proficient

Ok, I am new to this with my son being diagnosed this year, but I like to read up on things that will make big changes in my life...and if you have celiac disease even a speck of gluten can cause problems. You may not feel anything physically, but inside it is going to cause complications. Do you people read up on a serious disease you were diagnosed with????? Seriously, trace amounts of gluten add up and I am sorry but I am not putting my child at risk by allowing him something that contains the word malt in it. They are not safe, and if you truly care about yourself and you have celiac disease you will read up on what it does to your body when you consume gluten.

Here is some great advice....when in doubt, do without!!!!

Long time followers of the diet know that it is not possible to be 100% gluten free in our world. Gluten is everywhere, and you will encounter some.

Even products from so-called gluten-free facilities are subject to contamination from outside sources. At best, and at a high cost, products can be tested for gluten at 5 ppm. Mainstream manufacturers do not test at all, and "gluten-free" facilities which do test can only test to a detection limit. Glutino test to 20 ppm. El Peto test to 5 ppm. In both cases, it is probably zero, but that cannot be proven.

Your body regenerates at a certain rate. The celiac game is to keep the inevitable gluten ingestion at a level that the body heals faster than damage occurs.

Even assuming the worst case for content, ppm is not the whole answer. If I eat one slice of bread that has 20 ppm, or four slices of bread that have 5 ppm, the total amount of gluten is exactly the same in both cases. A tiny medicine tablet with 200 ppm would be less than even one slice of 5 ppm bread.

  • 5 months later...
dice401 Newbie

I realize this is an ages old post, but I just found this hot off the press:

Open Original Shared Link

  • 1 year later...
LisaB Newbie

I realize that the previous posts were from about 6 years ago, but for anyone currently wondering about Rice Krispies, this might be helpful. Lol 6 years later things are FINALLY getting better.

Open Original Shared Link

  • 4 weeks later...
zamm0 Apprentice

I'm glad this one has been dug up. The Celiac organisation Food Directory List says in the UK that Tesco own-brand Rice Krispies are within 20ppm. I've been eating them and my symptoms are quite mild anyway so hard to detect whether they are OK or not. My instinct is that Asda own brand Cornflakes are more innocuous FWIW. The problem with cereal in the 'Free From" isles of supermarkets is a) the packets are tiny and b ) they're very expensive, so was quite keen to work out which 'normal' products are OK.

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

      Issues before diagnosis

    2. - chrisinpa commented on Scott Adams's article in Skin Problems and Celiac Disease
      2

      Celiac Disease and Skin Disorders: Exploring a Genetic Connection

    3. - knitty kitty replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      My journey is it gluten or fiber?

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

      Issues before diagnosis

    5. - 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

  • 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
      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.  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
      @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
      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
      @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
      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.