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

Celiac's Vs Gluten Intolerance Diff?


Eric-C

Recommended Posts

caek-is-a-lie Explorer
I am convinced that the reason for this is that medical science is driven and funded by the pharmaceutical industry.

I am a scientist and I can tell you this is not entirely true. Medical science is also heavily funded by the government, specifically the NIH. The last 8 years have seen a serious erosion of scientific funding by the Bush administration, who didn't think science was important or compatible with their fundamentalist beliefs, and current economic times are making grants even harder to come by. A lot harder. We're just trying to keep our jobs right now.

There are probably a lot of scientists that would like to work on Celiac that may be having a difficult time obtaining funding to do their work, and it has nothing to do with pharma companies. So until the economy gets better, you'll have to wait for most of these great discoveries. It's going to take a few years longer than it otherwise would have, so please be patient. As a patient, I know science is agonizingly slow as it is. I hope you'll bear with us.


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



Celiac.com Sponsor (A8-M):



  • Replies 60
  • Created
  • Last Reply
Jestgar Rising Star
I am a scientist ...

cool. me too. what do you do?

caek-is-a-lie Explorer
I'm starting to think, in relation to my second paragraph that maybe Celiac's was incredibly rare, but as wheat flour usage grew so did it. When Enriched flours came out it skyrocketed.

Sorry for the third post in a row!

You are right, but there's even more to it than that. I was reading yesterday about studies on the developing immune system and the effects environmental toxins, viruses, and allergens have on the developing fetus's immune system, and that a lot of our autoimmune problems today and other diseases, whether they be in children or adult-onset, are caused by things babies are exposed to before they are born. For instance, diesel exhaust is linked to asthma.

Basically, if you are genetically predisposed to something, it can get triggered in the womb but not manifest itself until decades after you're born. Even Alzheimers! Celiac was even mentioned in the article, as was Autism. Considering the amount of toxins we have introduced to our environment in the last 100 years, I do not wonder why we have more incidences of diabetes, autism, celiac, alzheimers, adhd, etc., now than ever before in the history of man (and woman!)

So, add a world-wide excess abundance of wheat flour because it's cheap, combined with already compromised immune systems due to environmental factors, and you will see more cases of all these diseases across the board. And I would bet money that's not even the end of the story.

We are slowly destroying our species. If we go extinct, I have no doubt it will be by our own hand.

I don't have the link to the article here...it's at work, but I'll try to post it soon.

Fiddle-Faddle Community Regular
I am a scientist and I can tell you this is not entirely true. Medical science is also heavily funded by the government, specifically the NIH.

The members of NIH have serious financial ties to the pharmaceutical industry, according to mercola.com and several other sources, including Senator Dan Burton. The pharmaceutical industry is the strongest lobby there is.

I'm married to a scientist (who spent many years in DC, working for the government), so I'm not totally out of the loop!

I totally agree with your take on gluten intolerance.

caek-is-a-lie Explorer

Thanks, Fiddle-Faddle, and I believe you. You have a good point. Lobbying is a big problem in DC, and I don't believe for an instant that the NIH is immune. And don't get me started on the FDA. But at least when the NIH funds something, the pharmaceutical companies aren't right there in the lab dictating what we do. Maybe they influenced who got what money, but that's the end of it. We do what we do and that's it. When they're directly funding things, it gets much more complicated, and sometimes downright illegal. So sad what our country has become...

Tim-n-VA Contributor
Here's my take on it, and you are all free to differ. :)

Everyone here is gluten intolerant. It is the big umbrella we all sit under. None of us can tolerate gluten.

Some of us are Celiac, and our immune system is attacking our small intestines. Some of us have neurological problems, and our immune system is attacking our brains. Some of us have DH, and our immune system is attacking our skin.

But it is all because we cannot tolerate eating and/or touching gluten. So, no one is "just" gluten intolerant. We are all very gluten intolerant and we call it different things based on what part of the body it hurts most.

I would strongly agree with one caveat. I don't think - and I don't think you intended to imply - that your list of ways to be gluten intolerant is complete. Classic allergies are one example of an intolerance that is not the immune system attacking the body.

I would prefer the term gluten sensitive only because in some usage of intolerant is a digestive system inability to process a food (lactose intolerant).

ravenwoodglass Mentor
There are probably a lot of scientists that would like to work on Celiac that may be having a difficult time obtaining funding to do their work, and it has nothing to do with pharma companies. So until the economy gets better, you'll have to wait for most of these great discoveries. It's going to take a few years longer than it otherwise would have, so please be patient. As a patient, I know science is agonizingly slow as it is. I hope you'll bear with us.

I think one of the things that bothers me most is that there is a lot of research out there that is valid and way ahead of the research here in the US when it comes to celaic. But doctors here in the US seem clueless that it even exists. The reason in my opinion is that it is not controlled by drugs. We are very much a pharmacopic society we want instant fixes and doctors are very reluctant to even suggest a change in diet, they think we won't listen anyway. I saw this with celiac (it delayed my diagnosis by many painful years) and I saw this when a doctor told me I had diabetes. I learned nothing from the Diabetes educator, in fact I was handed a slew of papers, told to use them to line my bird cage and a script. When I asked about dietary changes I was told nothing other than to use sugar substitutes and take the pills, no other dietary changes were needed. I had to research stuff like a low glycemic diet on my own. My doctor was very upset that I refused to take the drugs and even more upset when I told him that with an A1C under 6 I disagreed with whether I was diabetic or not.

Doctors and researchers in this country really need to open their eyes, look at some of the research in other countries and try to trust us to be able to handle the changes we need to do. Or at least tell us about them.


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



Celiac.com Sponsor (A8-M):



leslieg Newbie
"We are slowly destroying our species. If we go extinct, I have no doubt it will be by our own hand."

As I've been cramming information about celiac for the past few days, I've thought more than once that this feels like our version of melamine-in-baby-formula.

My mom has always said she was "addicively allergic" to wheat. No one ever tested her for celiac. Now she has Altzheimer's. Is it related? I've spent a fortune on mental health care for me that, frankly, hasn't worked. I have an out-of-control child who has been to jail on assult charges and can't keep a job. Severe ADHD. But he would get so angry if you tried to prevent him from eating junk food. I have a child with spina bifida -- talk about a huge cost on every level. I took prenatal vitamins, but were they absorbed? My 7-year-old might be asperger's, or maybe just ADHD with sensory issues, and already we've paid thousands for therapies ... but he's had intestinal issues for years and has been followed by a GI ... and was never tested for celiac's. As I researched his issues I kept thinking he had such clear signs of rickets ... My 3-year-old is a carb-a-holic who won't use the potty if he doesn't get a treat. I find myself actually wanting thier tests to come back positive because then there won't be any excuses. The evil will be banned from my house. Period.

Fiddle-Faddle Community Regular

Welcome aboard, leslie, and I hope that celiac ends up being the answer to all your family's health problems!

It may sound awful to say "I hope your whole family has this disease," but I say it because I know that it's the easiest and cheapest disorder in the world to manage--a simple diet change, and everyone is perfectly healthy!

Good luck, and please keep us posted. And keep in mind that, no matter what the test results, you do NOT need a doctor's permission to start a gluten-free diet. If you need the doctor's say-so to convince relatives, then, if I were in your shoes, I'd be very tempted to go one step further--I'd LIE and say the doctor said to do the diet anyway. My family has been wonderful, though, so never needed to do it--but if I had to, I would.

I value honesty VERY VERY highly--but I value my family's health even more highly.

Eric-C Enthusiast

I had written out a nice big reply and the system seems to have lost it...thoughts for another day I guess.

Amber M Explorer
Many people with "just" gluten intolerance are actually in the early stage of celiac. They just don't have enough villi damage YET for a diagnosis.

Others with actual celiac are not tested properly, or even with proper testing, still show up as negative.

Then there are those who, according to current thought, are "only" gluten intolerant, but they suffer from multiple autoimmune diseases that are enough to put them in wheelchairs or worse. Those diseases miraculously seem to disappear on a gluten-free diet--which kind of shoots holes in the current thought that "just" gluten intolerance doesn't lead to deadly consequences.

There has been a lot of heated debate on this very topic on this board. The upshot is, you can talk all you want about the differences between celiac and "just" gluten intolerance, but in the final analysis, the cure and the outcome are both the same: either you follow a gluten-free diet, or you suffer ever-worsening systemic damage.

"You hit the nail on the head!" The book-"The Gluten Connection" explained a lot for me.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,563
    • Most Online (within 30 mins)
      7,748

    Bob Madden
    Newest Member
    Bob Madden
    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

    • Scott Adams
      Oats naturally contain a protein called avenin, which is similar to the gluten proteins found in wheat, barley, and rye. While avenin is generally considered safe for most people with celiac disease, some individuals, around 5-10% of celiacs, may also have sensitivity to avenin, leading to symptoms similar to gluten exposure. You may fall into this category, and eliminating them is the best way to figure this out. Some people substitute gluten-free quinoa flakes for oats if they want a hot cereal substitute. If you are interested in summaries of scientific publications on the topic of oats and celiac disease, we have an entire category dedicated to it which is here: https://www.celiac.com/celiac-disease/oats-and-celiac-disease-are-they-gluten-free/   
    • knitty kitty
    • knitty kitty
      Hi, @Ginger38, I've had shingles in the past.  I understand how miserable you're feeling.   Not only do i have the chickenpox virus lurking about, I also have the cold sore virus that occasionally flares with a huge cold sore on my lip when stressed or exposed to gluten.  The virus lives dormant in the nerves on the left side of my face.  It causes Bell's Palsy (resulting in drooling).  The cold sore virus is also in my eye.  My eye swells up and my vision is diminished permanently whenever I have a flare, so it's of the utmost importance to keep flares away and treat them immediately if they do happen so I don't lose any more vision.   I take the amino acid supplement L-Lysine.  Lysine messes with the replication of viruses, which helps the body fight them off.   I haven't had an outbreak for several years until this year when exceptionally stressed and contaminated, it flared up again. Lysine has been shown to be beneficial in suppression of viruses like the cold sore virus (a herpetic virus), the chickenpox virus (also a herpetic virus), as well as the HIV virus, and even the Covid virus.   I also take additional Thiamine in the form TTFD (tetrahydrofurfuryl disulfide) because Thiamine has antiviral properties as well.   For pain, a combination of Thiamine (like TTFD or Benfotiamine or Thiamine Hydrochloride), with B12 Cobalamine, and Pyridoxine B6 have been shown to have analgesic properties which relieve pain and neuropathy.    The combination of Thiamine B1, Pyridoxine B6 and Cobalamine B12 really does work to relieve pain.  I take it for back pain from crushed vertebrae in my back.  This combination also works on other pain and neuropathy.   I usually buy a supplement that combines all three and also Riboflavin B2 called EXPLUS online.  However, it's made in Japan and the price with the tariffs added makes it really expensive now.  But the combination of Thiamine B1, Pyridoxine B6 and B12 Cobalamine (and Riboflavin B2) still work even if taken separately.   I can't take Tylenol or ibuprofen because of stomach upsets.  But I can take the vitamin combination without side effects.  However, you can take the three vitamins at the same time as other pain relievers for added benefit.  The vitamins help other pain relievers work better. I hope you will try it.  Hopeful you'll feel better quickly. Interesting Reading: Thiamine, cobalamin, locally injected alone or combination for herpetic itching: a single-center randomized controlled trial https://pubmed.ncbi.nlm.nih.gov/23887347/ Mechanisms of action of vitamin B1 (thiamine), B6 (pyridoxine), and B12 (cobalamin) in pain: a narrative review https://pubmed.ncbi.nlm.nih.gov/35156556/ Analgesic and analgesia-potentiating action of B vitamins https://pubmed.ncbi.nlm.nih.gov/12799982/ A Narrative Review of Alternative Symptomatic Treatments for Herpes Simplex Virus https://pmc.ncbi.nlm.nih.gov/articles/PMC10301284/
    • Mari
      I think, after reading this, that you areso traumatized by not being able yo understand what your medical advisors have been  what medical conditions are that you would like to find a group of people who also feel traumatized who would agree with you and also support you. You are on a crusade much as the way the US Cabinet  official, the Health Director of our nation is in trying to change what he considers outdated and incorrect health advisories. He does not have the education, background or experience to be in the position he occupies and is not making beneficial decisions. That man suffered a terrible trauma early in his life when his father was assonated. We see now how he developed and worked himself into a powerful position.  Unless you are willing to take some advice or  are willing to use a few of the known methods of starting on a path to better health then not many of us on this Celiac Forum will be able to join you in a continuing series of complaints about medical advisors.    I am almost 90 years old. I am strictly gluten free. I use 2 herbs to help me stay as clear minded as possible. You are not wrong in complaining about medical practitioners. You might be more effective with a clearer mind, less anger and a more comfortable life if you would just try some of the suggestions offered by our fellow celiac volunteers.  
    • Jmartes71
      Thus has got to STOP , medical bit believing us! I literally went through 31 years thinking it was just a food allergy as its downplayed by medical if THEY weren't the ones who diagnosed us! Im positive for HLA-DQ2 which is first celiac patient per Iran and Turkey. Here in the States especially in Cali its why do you feel that way? Why do you think your celiac? Your not eating gluten so its something else.Medical caused me depression. I thought I was safe with my former pcp for 25 years considering i thought everything I went through and going through will be available when I get fired again for health. Health not write-ups my health always come back when you're better.Im not and being tossed away at no fault to my own other than shitty genes.I was denied disability because person said he didn't know how to classify me! I said Im celiac, i have ibs, hernia, sciatica, high blood pressure, in constant pain have skin and eye issues and menopause intensified everything. With that my celiac nightmare began to reprove my disregarded disease to a bunch of clowns who think they are my careteam when they said I didn't have...I feel Im still breathing so I can fight this so no body else has to deal with this nightmare. Starting over with " new care team" and waisting more time on why I think I am when diagnosed in 1994 before food eliminated from my diet. P.s everything i went through I did write to medical board, so pretty sure I will continue to have a hard time.
×
×
  • 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.