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.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

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

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,957
    • Most Online (within 30 mins)
      7,748

    Dogdad21
    Newest Member
    Dogdad21
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.