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

Caution On Gluten Free Alternatives


thomas3000

Recommended Posts

thomas3000 Rookie

A study has just been finished on Celiac and food sensitivities. It's amazing what was found. There are many people who have Celiac or are subclinically gluten intolerant. Up to 50 percent of the population is sensitive to Gluten. WOW! Meaning that they don't have celiac but are still sensitive to the Gliadin protein. Many celiacs still have residual symptoms after going gluten free and those are mainly headaches, neuropathy, depression, and anxiety disorders. Staying gluten free will eventually get rid of those symptoms but there is a way to do it within a weeks time and that's to test for further food allergies...The skin scratch test is only 10-15 percent accurate so the blood test for hidden allergies is the way to go.. The number 1 allergy that was found is Yeast, followed by dairy and eggs. Soy was on the list because it is antigenically similar to Gliadin. I really hope this helps some of you because I know some are still suffering even after going gluten free. The alternatives are good, but they still contain yeast, some with eggs and soy products and plenty of sugar. Once the gut heals you can start using these alternatives with caution. Many celiacs developed diabetes and heart disease even going gluten free because of the poor blood sugar regulation caused by the overconsumption of gluten free junk foods. Just because it doesn't contain gluten/gliadin doesn't mean it's healthy. York Labs has a reliable food allergy test and I would encourage those who are still suffering to get the ELISA food allergy panel....Best of luck to all and Merry Christmas!!!!God Bless..


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



Celiac.com Sponsor (A8-M):



Carriefaith Enthusiast

Thank you for posting that information. Do you have a link to the article? Or do you know where to find it?

traveljunkie Rookie

Thanks for the info! It answers a lot of questions about soy. I think I'll stay away from soy for a while, and see what happens when I re- introduce it! :)

Charlene

jerseyangel Proficient

Thanks Thomas--That was really interesting. I've recently been thinking about additional testing for other sensitivites. I would think it would make it so much easier to make choices. Merry Christmas to you :)

jenvan Collaborator

I'd like to see the article too. It would be shocking to me if yeast was #1 and not dairy or soy....

RiceGuy Collaborator
I'd like to see the article too. It would be shocking to me if yeast was #1 and not dairy or soy....

I'm not at all surprized about the yeast, since I discovered that long before the gluten part. Also when you realize that many so-called "health foods" use yeast because it will introduce MSG in a way that lets them avoid listing it on the label, it's no wonder why it's in so darn many prepackaged foods. MSG is known to cause migraines, and a host of other health problems. It damages the brain. Just Google for "yeast msg" and you'll be stunned.

Here's just a sample:

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

Here's something on casein:

Open Original Shared Link

thomas3000 Rookie

I'll post it when it is released. I was actually involved with the study so it may be a few months before it's posted on the internet. It was amazing what was found. Conventional medicine won't even accept that gluten causes all these problems. They also found that many celiacs suffer from dysbiosis in the gut which causes more food sensitivities. Probiotics are big in the recovery process as well has Hawthorne Berry Extract which aids in healing inflammation. The more I research the more I'm convinced that the FDA and AMA know this, but won't accept it because it eats into there revenue. If the CAUSE is found, then drugs and unnecessary surgery won't be needed. I always thought that Kevin Trudeau was a quack, but am slowly starting to believe him. I posted a few months ago about infections, and those were found in 80 percent of celiacs in the study. Mainly H. pylori, it's a bacteria found responsible for ulcers and stomach cancer. I even tested positive for it. Mastica gum kills it, or you can take the triple antibiotic therapy to clear it out. I chose the former. If it doesn't work then I'll take the medication to hopefully kill the bacteria. But, parasites were found in 8 of 10 patients as well. Maybe that has to do with other things going wrong, who knows.. More will be discovered in the near future and will keep all of you posted....


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



Celiac.com Sponsor (A8-M):



Carriefaith Enthusiast
I'll post it when it is released. I was actually involved with the study so it may be a few months before it's posted on the internet. It was amazing what was found.
I would love to see the article when it is done.
Claire Collaborator

Having faced the Delayed Food Alllergy problems long ago and gone the testing route - there is a word of caution.

These tests turn up a large number of false positives - making the results difficult to interpret, Things showup that you never ate in your life!

If anyone does choose the blood tests you need to look at what common reactives show up. Eliminate these. Then look at any that are foods you do eat but do not seem to have any reaction to. You can do a challenge on these. Eliminate for a couple of weeks. Then add back one food at a time - eat it every day for a week or until 'reaction' set in and you know to quit. If after a week there is no reaction you can assume that one was a false positive. ND's are turning away from these blood tests just because of the many false positives. I had about eight that were absolutely wrong. Claire

Nevadan Contributor
Having faced the Delayed Food Alllergy problems long ago and gone the testing route - there is a word of caution.

These tests turn up a large number of false positives - making the results difficult to interpret, Things showup that you never ate in your life!

Claire

I have had the same experience as Claire. I tested with York Labs IgG ELISA tests. They found reactions to all forms of gluten, wheat, etc and all dairy which is consistent with my dietary experiments; however, they also found several other reactions. I have never eaten some of these and the others I have eliminated and then resumed with no discernable effects.

George

thomas3000 Rookie

i'm just stating what i learned, that's all...Just trying to help, and I know this info will help many people who suffer with symptoms not related to gluten. Such as yeast, eggs, dairy, and soy. I know that gluten sets people up for these allergies, but further testing is still needed, because if you aren't allergic to eggs, then eating them is crucial for good health. Soy can be beneficial for some but not all. Not everyone is allergic to yeast, but some are and it's the main cause of symptoms in some people. This testing helps and takes the guesswork out of elimination diets and speculation. Don't play with your own health, that's all I'm saying and the testing proves that not everyone is the same...It's seems that whenever I discover something, somebody has to come in an give an opinion that's not based on science. If the testing comes up with allergies to foods that you're not eating, it basically means that your immune system is going haywire and is probably reacting to the smallest amounts of either ingested or inhaled substances. I would bet my life that most but not all depressive or anxious symptoms are food related, and we're finding that out with more and more research...

Nevadan Contributor
It's seems that whenever I discover something, somebody has to come in an give an opinion that's not based on science. If the testing comes up with allergies to foods that you're not eating, it basically means that your immune system is going haywire and is probably reacting to the smallest amounts of either ingested or inhaled substances. I would bet my life that most but not all depressive or anxious symptoms are food related, and we're finding that out with more and more research...

I assume you may be referring to my previous post. I wasn't knocking your point that other antigens often cause lingering problems. I was just stating my observation about my experience with the York testing not leading to obvious cause/effect relationships which I found very disappointing. My intuitive feeling is that having multiple reactions show up may be more indictive of a leaky gut. The immune system may be just doing what it's supposed to do when foreign material gets into the bloodstream. The foreign material could be coming from any number of unknown sources. The presence of some of these antibodies may not cause any symptoms, or damage; however, gluten and casein proteins have been shown capable of causing damage; there are probably others as well. I've been gluten-free/CF for several months and after a year or so when a leaky gut might have had time to heal, I may retest with York to see if the number of reactions has decreased.

I also agree with your statements regarding possible coverup from our medical organizations, big pharma, food business, etc. Particularly big pharma would take a huge financial hit if only a few of the benefits of gluten-free/CF were to be realized in the general population, not to mention the grain and dairy businesses.

So far one of the biggest issues is how to get people to take some responsibility for their health and even try eliminating some of these antigens. From my personal experience with friends and family and from posts I see here, there is a huge resistance to changing eating habits, no matter what the benefits might be.

George

Claire Collaborator
So far one of the biggest issues is how to get people to take some responsibility for their health and even try eliminating some of these antigens. From my personal experience with friends and family and from posts I see here, there is a huge resistance to changing eating habits, no matter what the benefits might be.

George

George - you sure got that one right.!!!!! Claire

lgleeson Newbie

I just want to say that everyone that has any kind of condition always assumes that there is a cover up at the pharmaceutical companies. I just want to say, as a scientist at a drug company, who also has Celiac, we all have mothers and fathers and sisters, too and a lot of them have diseases that we would love to be able to cure.

Claire Collaborator

Thomas:

I don't know whether you were responding here to George or to me. Regardless, let this be said: this is a forum and people come here with information and personal opinions as well. Of course you meant to be helpful - so do I - but your post here suggests that you don't much welcome anyone not agreeing with you.

I certainly do agree with some things you said. When it comes to the allergy testing, I most definitely do not. I think it misleading to suggest that elimination diets are guesswork and speculation or that allergy blood testing is definitive. Neither is true. This also implies that we cannot trust our own bodies but we can trust the lab results.

I and people I know have had these tests. I actually had them three times. So in the first place I speak from experience. Secondly, I have the opinion of a highly respected ND who has stopped using these tests for his patients because he became so concerned that many were eliminating valuable nutrition from their diets based on test results - when many of the identified foods posed no problem. These patients were assisted through 'challenges' - as some have done with gluten - i.e. delete a food for some time and then reintroduce it and eat it regularly. If there is no reaction that food remains available to you. But in order to clarify the tests you still wind up having to do the elimination - challenge - etc.- the very thing you seem to think is guesswork. I have included at the end here an article on this subject that is well worth reading.

Regarding this statement" " If the testing comes up with allergies to foods that you're not eating, it basically means that your immune system is going haywire and is probably reacting to the smallest amounts of either ingested or inhaled substances." Says who? Do you have some 'Scientific" reference for this statement?

You say "It's seems that whenever I discover something, somebody has to come in an give an opinion that's not based on science" I don't see any scientific, professional references in anything you have posted. Again, I remind you that this a forum - people do 'come in and give an opinion'.

I believe the experience of NDs with their patients is a valid reference in support of opinion on these tests. Even if you disgard personal experiences which you seem inclined to do - there are still sufficeint articles available by reputable professionals on this subject to warrant investigation. One such reference is listed here. You can certainly find many others. Claire

IgG FOOD ALLERGY TESTING BY ELISA/EIA - What Do They Really Tell Us?

Open Original Shared Link

thomas3000 Rookie

I know 2 people personally who suffered years and years with depressive/anxiety symptoms. They were treated with guess what??? Antidepressants that didn't work. After the years of suffering they both went through allergy testing, and found yeast allergies and a few others. They cut out the offended food and WHAM! The depression lifted and the anxiety disappeared. It's beneficial trust me on that one, but it's not the only thing to do. You must be checked for infections. Parasitic, bacterial, and fungus can cause food allergies as well. I'm not saying that allergy testing is the cure all, but it's beneficial to many. My uncle had a hidden peanut allergy, he didn't have an immediate reaction, but a delayed onset. He cut out peanuts and his skin cleared up completely and feels a lot more energetic. It's just a peice of the puzzle and only a part of the healing process.

Nevadan Contributor
I just want to say that everyone that has any kind of condition always assumes that there is a cover up at the pharmaceutical companies. I just want to say, as a scientist at a drug company, who also has Celiac, we all have mothers and fathers and sisters, too and a lot of them have diseases that we would love to be able to cure.

Hello Igleeson,

I hear you and apologize for my generalizations; however, it does get pretty frustrating when there seems to be evidence that some, not all I'm sure, suffering from some pretty common maladies such as arthritis, osteoporosis, anemia, reflux(heartburn), etc only get prescribed expensive drugs that usually treat only the symptoms, not the root causes. Maybe the real problem is that so many dr's seem to depend almost exclusively on the pharma salespeople for their continuing education - no drug, no real ailment, "its all in your head". This is even more frustrating when a possible cure is as simple, and cheap, as a good gluten-free diet.

Welcome to the board. Hopefully you can add a new dimension here. I look forward to future posts.

George

thomas3000 Rookie

Oh, and by the way, If you ever get glutened or eat a food and get a reaction, Alka-Seltzer gold stops the reaction....Merry Christmas again!!

Rachel--24 Collaborator
Maybe the real problem is that so many dr's seem to depend almost exclusively on the pharma salespeople for their continuing education - no drug, no real ailment, "its all in your head". This is even more frustrating when a possible cure is as simple, and cheap, as a good gluten-free diet.

I agree George,

I just saw a doctor who believes in finding the root cause of symptoms rather than treating them with meds.

He said his "pet peeve" was doctors who believe "it's all in your head" just because tests are negative or they cant perscribe a drug to "fix" the problem. He said when something shows up in a test that they can "understand" and perscribe something for they will jump into action. He used my Graves Disease as an example..he was right...the docs DID jump into action when they saw those test results. I had completely opposite experience with getting my gluten intolerance recognized....at one point my bathroom looked like a small pharmacy. They love whipping out that prescription pad and when I started refusing the drugs and demanding they search for a cause...I was told to see the psychiatrist and get put on antidepressants. :angry:

Its sad but the majority of doctors out there think and act in this manner.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,855
    • Most Online (within 30 mins)
      7,748

    Tara M
    Newest Member
    Tara M
    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
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
    • Francis M
      Thanks. Since the back and forth and promises of review and general stalling went on for more than six months, the credit company will no longer investigate. They have a cutoff of maybe six months.
×
×
  • 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.