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

Organic Foods Threatened


ginghamkim

Recommended Posts

ginghamkim Apprentice

Has anyone watched the documentary The Future of Food (more information at www.thefutureoffood.com)? I watched it last night and was horrified to learn that the US Government does not enforce that genetically modified foods (GMO)/ingredients have to be labeled. The European Union enforces labeling laws on GMO and Japan even bans gmo imports. If you get a chance, watch this documentary (netflix) and you will learn so much.

I came from a farm and we did everything that the documentary profiled because we didn't know any better and both my parents had cancer (that's right, we had wheat crop every year too, ah irony...I used to eat it raw from the hopper wagons). :huh: Just FYI---we would by corn seed every year that had a pink coating so that rats/mice/insects would not eat it. The corn ears that it would grow was sterile, so that you would have to buy new seed every year.

Anyway, the problem is that gmo seed and pollen can contaminate our precious organic foods and the USDA is not doing anything to stop it (it has to do with patent laws). I am writing my congress person using this site... The Campaign to Label Genetically Engineered Foods www.thecampaign.org.

This is very serious...I am not an activist but a concerned citizen. How many of you rely completely on organic food since you became gluten-free? Please take some time to look into genetically modified food and make your own decisions.

Kim


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



Celiac.com Sponsor (A8-M):



gfp Enthusiast

I have to say this is one of those issues people ignore or think they will worry about later.

Its really not like that, later will be too late once the GM crops have cross pollented... sure theoretically they are not meant to but this is nature, albeit a frankenstein equavalent.

When you grow hundreds of millions of GM crops every year one of them will mutate, nothing is more certain over time.

I'm not saying Jurassic park is a scientifically accurate film but the point were the guy says "They can't breed" is pretty spot on...

Breeding is the primary directive of all life... nature will find a way and always does.

If GM foods were not so actively opposed by gruops who go over the top in other things perhaps more people would take this seriously.

ginghamkim Apprentice

The big problem is that mega companies can patent gmo seed. If the gmo seed cross pollinates with an organic farmer's crop, takes on the characteristics of the patented gmo seed, the mega company can claim that it is infringement and the courts will demand that the organic farmer's seed/plant be destroyed. If the organic farmer has to destroy his seed, then he cannot plant the organic (non-gmo) crop next year.

Imagine this on a larger scale and there would be no organic farming with non-gmo seed.

This is not hypothetical, this is already happening to American Farmers.

We have power as consumers...let's look at Europe as an example.

tummytroubles Newbie

I just saw the movie a couple of nights ago with my husband. Our local library had it. I'm definitely going to get more involved, as well as tell everyone I know. It's so frustrating that genetically modified food doesn't have to be labelled, and that through no fault of their own, organic farmer's crops are getting cross pollenated by this stuff. Who knows how many people are allergic and/or sensitive to these new forms of food.

Thanks for starting this thread and making more people aware :-)

Felidae Enthusiast

I learned about GMO's in several of my classes, one of them being Botany. It sure is a very interesting topic. Europe has a completely different viewpoint than the US and Canada.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,898
    • Most Online (within 30 mins)
      7,748

    MLucia
    Newest Member
    MLucia
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Welcome to the forum, @Judy M! Yes, he definitely needs to continue eating gluten until the day of the endoscopy. Not sure why the GI doc advised otherwise but it was a bum steer.  Celiac disease has a genetic component but also an "epigenetic" component. Let me explain. There are two main genes that have been identified as providing the "potential" to develop "active" celiac disease. We know them as HLA-DQ 2.5 (aka, HLA-DQ 2) and HLA-DQ8. Without one or both of these genes it is highly unlikely that a person will develop celiac disease at some point in their life. About 40% of the general population carry one or both of these two genes but only about 1% of the population develops active celiac disease. Thus, possessing the genetic potential for celiac disease is far less than deterministic. Most who have the potential never develop the disease. In order for the potential to develop celiac disease to turn into active celiac disease, some triggering stress event or events must "turn on" the latent genes. This triggering stress event can be a viral infection, some other medical event, or even prolonged psychological/emotional trauma. This part of the equation is difficult to quantify but this is the epigenetic dimension of the disease. Epigenetics has to do with the influence that environmental factors and things not coded into the DNA itself have to do in "turning on" susceptible genes. And this is why celiac disease can develop at any stage of life. Celiac disease is an autoimmune condition (not a food allergy) that causes inflammation in the lining of the small bowel. The ingestion of gluten causes the body to attack the cells of this lining which, over time, damages and destroys them, impairing the body's ability to absorb nutrients since this is the part of the intestinal track responsible for nutrient absorption and also causing numerous other food sensitivities such as dairy/lactose intolerance. There is another gluten-related disorder known as NCGS (Non Celiac Gluten Sensitivity or just, "gluten sensitivity") that is not autoimmune in nature and which does not damage the small bowel lining. However, NCGS shares many of the same symptoms with celiac disease such as gas, bloating, and diarrhea. It is also much more common than celiac disease. There is no test for NCGS so, because they share common symptoms, celiac disease must first be ruled out through formal testing for celiac disease. This is where your husband is right now. It should also be said that some experts believe NCGS can transition into celiac disease. I hope this helps.
    • Judy M
      My husband has had lactose intolerance for his entire life (he's 68 yo).  So, he's used to gastro issues. But for the past year he's been experiencing bouts of diarrhea that last for hours.  He finally went to his gastroenterologist ... several blood tests ruled out other maladies, but his celiac results are suspect.  He is scheduled for an endoscopy and colonoscopy in 2 weeks.  He was told to eat "gluten free" until the tests!!!  I, and he know nothing about this "diet" much less how to navigate his in daily life!! The more I read, the more my head is spinning.  So I guess I have 2 questions.  First, I read on this website that prior to testing, eat gluten so as not to compromise the testing!  Is that true? His primary care doctor told him to eat gluten free prior to testing!  I'm so confused.  Second, I read that celiac disease is genetic or caused by other ways such as surgery.  No family history but Gall bladder removal 7 years ago, maybe?  But how in God's name does something like this crop up and now is so awful he can't go a day without worrying.  He still works in Manhattan and considers himself lucky if he gets there without incident!  Advice from those who know would be appreciated!!!!!!!!!!!!
    • Scott Adams
      You've done an excellent job of meticulously tracking the rash's unpredictable behavior, from its symmetrical spread and stubborn scabbing to the potential triggers you've identified, like the asthma medication and dietary changes. It's particularly telling that the rash seems to flare with wheat consumption, even though your initial blood test was negative—as you've noted, being off wheat before a test can sometimes lead to a false negative, and your description of the other symptoms—joint pain, brain fog, stomach issues—is very compelling. The symmetry of the rash is a crucial detail that often points toward an internal cause, such as an autoimmune response or a systemic reaction, rather than just an external irritant like a plant or mites. I hope your doctor tomorrow takes the time to listen carefully to all of this evidence you've gathered and works with you to find some real answers and effective relief. Don't be discouraged if the rash fluctuates; your detailed history is the most valuable tool you have for getting an accurate diagnosis.
    • Scott Adams
      In this case the beer is excellent, but for those who are super sensitive it is likely better to go the full gluten-free beer route. Lakefront Brewery (another sponsor!) has good gluten-free beer made without any gluten ingredients.
    • trents
      Welcome to the forum, @catsrlife! Celiac disease can be diagnosed without committing to a full-blown "gluten challenge" if you get a skin biopsy done during an active outbreak of dermatitis herpetiformis, assuming that is what is causing the rash. There is no other known cause for dermatitis herpetiformis so it is definitive for celiac disease. You would need to find a dermatologist who is familiar with doing the biopsy correctly, however. The samples need to be taken next to the pustules, not on them . . . a mistake many dermatologists make when biopsying for dermatitis herpetiformis. 
×
×
  • 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.