Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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 Celiac.com!
    eNewsletter
    Donate

Cranberry Juice, Vitamin Supplements,tofu (And More)


nodrog

Recommended Posts

nodrog Newbie

For several months I had been, and have been, having trouble with an excess amount of gas, bloated abdomen, and so on. My primary physician suggested I take Beano and simethicone to relieve these symptoms.  These didn't seem to be working, so he sent me to have blood work done and to provide stool samples.  None of these tests resulted in anything that stood out.  He then had me get a cat scan.  Again, nothing stood out. (Meanwhile he had me continue taking the Beano and simethicone) In desperation, or perhaps in exasperation, he referred me to a gasterenterolgist.   The gasterenterologist  had me stop taking the Beano and simethicone and instead has me on a probiotic (Align). He also had me stop taking the antibiotic medication I was using to manage a urinary tract infection. He, too, sent me to have blood work done and to provide stool samples.  In adition, he sent me to have xrays and a flouroscopy done. He has me scheduled for a followup appointment this coming Tuesday.  And he suggested I might be allergic to celiac and gluten intolerant, which has lead me to ask the following questions. 

 

If a product is not labeled gluten-free, does that mean it is not gluten-free? Do some food producers not think it is important to label something gluten-free or not? For example the tofu I buy at Trader Joe's is not labeled gluten-free, but I had read somewhere that tofu in general is gluten-free. My local Trader Joe's has a list of gluten-free products, probably a nation-wide generated list.  The list indicates that the Trader Joe's canned pink salmon is gluten-free, but the can says nothing about being gluten-free.

 

I also drink Langer's Zero Sugar Added Cranberry Joice to ward off urinary tract infections, but the label says nothing about it being gluten-free.  What should I be reading on the juice label ingredients to warn me if I am gluten intolerant?

 

How about vitamin supplements?  I noticed that the fourth ingredient on my Centrium multivitamin shows Mannitol (Wheat), so I guess I'll have to stop taking this supplement.  This leads me to another question.  For over twenty years, I have had an ileostomy.  That means, among other things, that I cannot use gel forms of medications because I cannot absorb them properly. Instead, I need to take capsule, chewable, or liquid forms of medication.  (I use a fish oil omega three supplement, instead of a gel tablet.)

 

I know these are lot of questios to pose for a first post, and I even may have omitted some questions that slipped my mind, but I would greatly appreciate your advice and suggestions and eagerly await your responses.

 

Thank you very much.

 

 

Gordon

 

(By the way, the Align doesn't seem to be having any affect on my symptoms.)

 

 

 

 

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



Mr. GF in Indiana Newbie

First congrats on using doctors to pursue your difficulty. However, if he wants to test you later for

villous atrophy (celiac gut damage) you need to keep eating gluten for now. The test could turn up

negative, you could still be gluten sensitive even so, just not "celiac".

Labels in the US are unregulated as to wheat content (or corn, for that matter...lots of people have trouble with corn, celiac or not). You take your chances, check the "search" function on celiac.com for foods and drugs by brand name, lots of information here. You can, if the food is important enough, buy test kits for wheat gluten down to 20 ppm sensitivity or better.

Your statistical odds of having "celiac" or "gluten sensitivity" WITH provable symptoms or consequences, are actually very small, meaning your problems can also be one of many other unfortunate conditions. Open Original Shared Link

Open Original Shared Link

I used align, found it worthless and most probiotics don't do much for most people (unless they are just finished with antibiotic).

In order best to find out what foods and problems you may have...if any can be proven...consider doing an "elimination diet" where you find foods that don't trigger the symptoms, no matter how narrow that may be, then add one food at a time until you think you have the symptoms, repeat, and do research on the internet. This can require considerable discipline and a long time and multiple trials. I found sites such as rightdiagnosis.com to be helpful. Avoid jumping to conclusions; if you focus on one medical condition, use pubmed.com to read the articles description (and limits of each study) for yourself. Also check rxlist.com for all of your medication cross-reactions, it's surprising how difficult it is to avoid side effects as well (since many gut problems come from medications).

Link to comment
Share on other sites
kareng Grand Master

,

Labels in the US are unregulated as to wheat content (or corn, for that matter...lots of people have trouble with corn, celiac or not). ).

This is not true. In the US, wheat falls under the Allergen labeling laws. It must be declared in a food ingredients.

Corn is considered safe for Celiacs.

Link to comment
Share on other sites
notme Experienced

 I noticed that the fourth ingredient on my Centrium multivitamin shows Mannitol (Wheat), so I guess I'll have to stop taking this supplement.  This leads me to another question. 

 

mannitol is a sugar alcohol derived from a sugar 

Link to comment
Share on other sites
cyclinglady Grand Master

I can address the probiotic.  Its purpose is to re-populate your intestinal tract with good bacteria.   After ending a course of a broad-spectrum antibiotic, you often wipe out or reduce both "good and bad" bacteria.  (Everyone (bacteria and fungus) is jockeying for wall space!)  An unbalanced intestinal tract can lead to all kinds of problems (fungal, bad bacterial over-growth, etc.)

 

So, probiotics are beneficial but don't help with immediate symptoms.  My MD began recommending them almost 20 years ago after ever course of antibiotics he prescribed. I even give them to my dog after she's been given antibiotics.  

Link to comment
Share on other sites
Mr. GF in Indiana Newbie

This is not true. In the US, wheat falls under the Allergen labeling laws. It must be declared in a food ingredients.

Corn is considered safe for Celiacs.

Please feel free to believe whatever works for you and whatever you like. Where I live however, wheat is neither labeled on food cans sitting in my own kitchen, if one knows the hundreds of names under which wheat ingredients hide, or has called the manufacturer (example, wheat is used to act as a paste in wine barrels and to "fine" the wine...think that's disclosed?).

Due to my wheat gluten-identical reactions to eating any corn (maize) I have researched this extensively. It is shown conclusively up to half of "celiacs" show an inflammatory response to corn, demonstrated in a "rectal challenge".

Open Original Shared Link

The same test is used to show that celiacs react chemically to casein (the protein in milk, which is almost identical to the gluten protein). "A mucosal inflammatory response similar to that elicited by gluten was produced by CM protein in about 50% of the patients with coeliac disease. Casein, in particular, seems to be involved in this reaction." Open Original Shared Link

Also, sorghum (a very close corn relative but a major food crop) is thought to be safe for "celiacs"; it isn't if the problem is a prolamin problem, not merely a wheat gluten problem (beware cross contamination, of course).

NOTE: there are about twenty-five thousand medical articles on celiac (coeliac) in worldwide medical journals just in English language alone (see, pubmed.com and other search engines). Please see the Cochrane reviews as to the low quality of many studies and their general statistical methods and reliability or undisclosed conflicts of interest.

Link to comment
Share on other sites
kareng Grand Master

Please feel free to believe whatever works for you and whatever you like. Where I live however, wheat is neither labeled on food cans sitting in my own kitchen, if one knows the hundreds of names under which wheat ingredients hide, or has called the manufacturer (example, wheat is used to act as a paste in wine barrels and to "fine" the wine...think that's disclosed?).Due to my wheat gluten-identical reactions to eating any corn (maize) I have researched this extensively. It is shown conclusively up to half of "celiacs" show an inflammatory response to corn, demonstrated in a "rectal challenge".Open Original Shared LinkThe same test is used to show that celiacs react chemically to casein (the protein in milk, which is almost identical to the gluten protein). "A mucosal inflammatory response similar to that elicited by gluten was produced by CM protein in about 50% of the patients with coeliac disease. Casein, in particular, seems to be involved in this reaction." Open Original Shared LinkAlso, sorghum (a very close corn relative but a major food crop) is thought to be safe for "celiacs"; it isn't if the problem is a prolamin problem, not merely a wheat gluten problem (beware cross contamination, of course).NOTE: there are about twenty-five thousand medical articles on celiac (coeliac) in worldwide medical journals just in English language alone (see, pubmed.com and other search engines). Please see the Cochrane reviews as to the low quality of many studies and their general statistical methods and reliability or undisclosed conflicts of interest.

I will state once again, in the US, wheat as an ingredient in food cannot " hide". If you believe a manufacturer is " hiding " gluten in a food and have proof of that, you should report it. There is a way to do that on the FDA website, I believe.

But seriously...from that study you cited, it doesn't mention corn. The second study gave them gluten with the milk protein.

"Rectal challenge with gluten results in increased luminal levels of NO in a group of patients with treated coeliac disease. Further studies are needed to evaluate the role of NO in coeliac disease and the potential usefulness of rectal NO measurements in aiding diagnosis of this intestinal disorder."

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Here's the link so you can report the unlabeled gluten foods you have purchased

Open Original Shared Link

Link to comment
Share on other sites
IrishHeart Veteran

and most probiotics don't do much for most people (unless they are just finished with antibiotic).

 

 

I am afraid I have to disagree with you, strongly on this one  (and I will get to the erroneous statement about wheat paste and wine later <_< maybe )

.

Dr. Guandalini of the Univ.of Chicago Celiac Center has written an article in the book Real Life With Celiac Disease

by Melinda Dennis and Daniel Leffler about probiotics and their usefulness in treating inflammation in celiac's guts.

 

Other articles have been published in Pub Med that show that they help reduce inflammation in  the gut in people with microscopic colitis, C. Diff, IBS  and Crohn's. etc..

 

A wide spread statement like "most probiotics don't do much for most people" because  is simply untrue.

Many people on this site will attest to their usefulness.

They have helped me enormously as I had no detectable levels of beneficial gut bacteria upon DX and my GI tract was in flames. I am right as rain for the first time in life and my own GI doctor believes in their efficacy.

 

This article sheds some light for the OP:

 

Open Original Shared Link

Link to comment
Share on other sites
IrishHeart Veteran

. It is shown conclusively up to half of "celiacs" show an inflammatory response to corn, demonstrated in a "rectal challenge".

Open Original Shared Link

 

 

 

Why do you use " " around the word "celiacs"?? just curious.

 

Ok, here is what I saw in this Pub Med article:

 

" The aim of this study was to evaluate whether rectal challenge with gluten would trigger an increased local production of the gas nitric oxide (NO), a novel marker of intestinal inflammation"

 

"20 patients with treated coeliac disease and in 13 healthy controls. Luminal levels of NO were measured in the rectum ".

 

How on earth does a study of 20 patients undergoing a rectal challenge with gluten ....show an inflammatory response to corn?????

Link to comment
Share on other sites
Lisa Mentor

You will need to read lables and also make some judgement calls.

 

The US labeling law is not in place yet, but hopefully soon.  Until then, it's voluntary without regulation.

 

Wheat is required, due the allergin law, to be listed.  And sometimes you have to deside if a product includes malt or barley.  Or call the manufacturer.

 

Certified Gluten Free Products ARE tested to be withing the safe limites for most people with Celiac.

 

I generally read the labels of companies that will always disclose all forms of gluten, such as Kraft, Unilever and Hormel  (I think I'm missing one...)  But, still...nothing goes into my cart without me reading the label.
 

Link to comment
Share on other sites
Mr. GF in Indiana Newbie

Hmm...here's the study on corn.  Open Original Shared Link.  I missed.  Since I have over 5000 celiac-oriented articles copied and indexed, clicking the slightly wrong place is rather a hazard of computers.  If anyone has further questions or thoughts on what that all means, or the reason that corn gluten and casein resemble and act on many people in the identical way as if it is wheat gluten (because on a molecular level of the important fraction, it is in general)...feel free to do your own research on PubMed, on its British equivalent, and the French and German versions, and draw your own conclusions (although it seems most major German studies are getting into English...but not all). Every study has its limitations, unfortunately.   Note:  use the word "maize" as well as "corn".  Also, scientists use the word "celiac" in all sorts of senses, one quickly learns that each has a different definition (also, "coeliac" if one is British, Maladie cœliaque if French, etc).      

 

I find that amazon has the largest list of gluten free packaged foods, but I am able to get them locally so far and haven't had to order from them, but the list is useful, maybe you can find the products you like in a competing, but marked "gluten free" package?      

Link to comment
Share on other sites
kareng Grand Master

Hmm...here's the study on corn. Open Original Shared Link. I missed. Since I have over 5000 celiac-oriented articles copied and indexed, clicking the slightly wrong place is rather a hazard of computers. If anyone has further questions or thoughts on what that all means, or the reason that corn gluten and casein resemble and act on many people in the identical way as if it is wheat gluten (because on a molecular level of the important fraction, it is in general)...feel free to do your own research on PubMed, on its British equivalent, and the French and German versions, and draw your own conclusions (although it seems most major German studies are getting into English...but not all). Every study has its limitations, unfortunately. Note: use the word "maize" as well as "corn". Also, scientists use the word "celiac" in all sorts of senses, one quickly learns that each has a different definition (also, "coeliac" if one is British, Maladie cœliaque if French, etc).

I find that amazon has the largest list of gluten free packaged foods, but I am able to get them locally so far and haven't had to order from them, but the list is useful, maybe you can find the products you like in a competing, but marked "gluten free" package?

..6 people had a slight reaction to someone putting corn in their rectum.

Some of these studies of 10-20 patients that you keep putting on this forum actually say that they are just a preliminary study and more in depth study needs to be made.

If corn bothers you....sorry. don't eat it. But to say that a large % of Celiacs can't eat it safely is not in align with current recommendations.

Open Original Shared Link

Link to comment
Share on other sites
nodrog Newbie

This is all very confusing, but thanks for all the responses. I'm sorry not to have replied sooner, but I keep on getting locked out.

 

 

Gordon

Link to comment
Share on other sites
kareng Grand Master

This is all very confusing, but thanks for all the responses. I'm sorry not to have replied sooner, but I keep on getting locked out.

Gordon

Sorry you thread got hijacked.

To answer your question about foods labelled gluten-free. In the US, there is no definition of gluten-free. Many companies choose to test for gluten and label gluten-free. Some label gluten-free if they use no gluten in the product. Many don't bother to label gluten-free but that doesn't mean there is gluten in the ingredient. For example, canned tomatoes - ingredients : tomatoes, water, salt. That is gluten-free. Probably not labelled gluten-free or tested for gluten as ere is no reason to add that expense to the product.

Because we have no law for what is gluten-free, many companies are waiting to label things gluten-free. Also, its a bit misleading for a company to label an apple as gluten-free. It is naturally gluten-free.

We're you tested for Celiac? You should not eat gluten-free until all the testing is done or they might come up negative. You produce the antibodies and the damage, that is being tested for, when eating gluten. No gluten, no antibodies, basically. Also, Celiac isn't an allergy it is an autoimmune disease.

Have you read the Newbie thread? A lot of basic info there.

Let me get the link

https://www.celiac.com/forums/topic/91878-newbie-info-101/

Link to comment
Share on other sites
nodrog Newbie

Sorry you thread got hijacked.

To answer your question about foods labelled gluten-free. In the US, there is no definition of gluten-free. Many companies choose to test for gluten and label gluten-free. Some label gluten-free if they use no gluten in the product. Many don't bother to label gluten-free but that doesn't mean there is gluten in the ingredient. For example, canned tomatoes - ingredients : tomatoes, water, salt. That is gluten-free. Probably not labelled gluten-free or tested for gluten as ere is no reason to add that expense to the product.

Because we have no law for what is gluten-free, many companies are waiting to label things gluten-free. Also, its a bit misleading for a company to label an apple as gluten-free. It is naturally gluten-free.

We're you tested for Celiac? You should not eat gluten-free until all the testing is done or they might come up negative. You produce the antibodies and the damage, that is being tested for, when eating gluten. No gluten, no antibodies, basically. Also, Celiac isn't an allergy it is an autoimmune disease.

Have you read the Newbie thread? A lot of basic info there.

Let me get the link

https://www.celiac.com/forums/topic/91878-newbie-info-101/

Thanks for your reply, kareng.  Yes I did read that link.

 

 

gordon

Link to comment
Share on other sites
kareng Grand Master

For several months I had been, and have been, having trouble with an excess amount of gas, bloated abdomen, and so on. My primary physician suggested I take Beano and simethicone to relieve these symptoms.  These didn't seem to be working, so he sent me to have blood work done and to provide stool samples.  None of these tests resulted in anything that stood out.  He then had me get a cat scan.  Again, nothing stood out. (Meanwhile he had me continue taking the Beano and simethicone) In desperation, or perhaps in exasperation, he referred me to a gasterenterolgist.   The gasterenterologist  had me stop taking the Beano and simethicone and instead has me on a probiotic (Align). He also had me stop taking the antibiotic medication I was using to manage a urinary tract infection. He, too, sent me to have blood work done and to provide stool samples.  In adition, he sent me to have xrays and a flouroscopy done. He has me scheduled for a followup appointment this coming Tuesday.  And he suggested I might be allergic to celiac and gluten intolerant, which has lead me to ask the following questions. 

 

If a product is not labeled gluten-free, does that mean it is not gluten-free? Do some food producers not think it is important to label something gluten-free or not? For example the tofu I buy at Trader Joe's is not labeled gluten-free, but I had read somewhere that tofu in general is gluten-free. My local Trader Joe's has a list of gluten-free products, probably a nation-wide generated list.  The list indicates that the Trader Joe's canned pink salmon is gluten-free, but the can says nothing about being gluten-free.

 

I also drink Langer's Zero Sugar Added Cranberry Joice to ward off urinary tract infections, but the label says nothing about it being gluten-free.  What should I be reading on the juice label ingredients to warn me if I am gluten intolerant?

 

How about vitamin supplements?  I noticed that the fourth ingredient on my Centrium multivitamin shows Mannitol (Wheat), so I guess I'll have to stop taking this supplement.  This leads me to another question.  For over twenty years, I have had an ileostomy.  That means, among other things, that I cannot use gel forms of medications because I cannot absorb them properly. Instead, I need to take capsule, chewable, or liquid forms of medication.  (I use a fish oil omega three supplement, instead of a gel tablet.)

 

I know these are lot of questios to pose for a first post, and I even may have omitted some questions that slipped my mind, but I would greatly appreciate your advice and suggestions and eagerly await your responses.

 

Thank you very much.

 

 

Gordon

 

(By the way, the Align doesn't seem to be having any affect on my symptoms.)

 

Looks like your juice actually says its gluten-free.  Most juice would be gluten-free.  Besides an obvious wheat ingredient (not likely in a juice), it could list barley malt or just malt as a sweetener.  Its an expensive sweetener and not used very often.

 

.Open Original Shared Link

Link to comment
Share on other sites
nodrog Newbie

Looks like your juice actually says its gluten-free.  Most juice would be gluten-free.  Besides an obvious wheat ingredient (not likely in a juice), it could list barley malt or just malt as a sweetener.  Its an expensive sweetener and not used very often.

 

.Open Original Shared Link

Thanks for that link.  I looked pretty carefully on the bottle, but I didn't see "gluten-free" on the label.

 

 

gordon

Link to comment
Share on other sites
notme Experienced

gordon:   what are the ingredients on your juice - is it just plain fruit juice?  or if not, what exactly is added to it?

Link to comment
Share on other sites
kareng Grand Master

gordon:   what are the ingredients on your juice - is it just plain fruit juice?  or if not, what exactly is added to it?

 

 

On the website for the juice it says all their juices are gluten-free.  So I gave him the link.

Link to comment
Share on other sites
notme Experienced

On the website for the juice it says all their juices are gluten-free.  So I gave him the link.

oops, sorry, k - didn't look at the link - i'm the warden at the stoopit prison today :)

 

edited to add:  babysitting my niece and nephew lolz - yes, you must eat lunch!!

Link to comment
Share on other sites
nodrog Newbie

Oatmeal can be problematic, so I pose this question,.I have been buying John McCann Steel Cut Irish Oatmeal from Trader Joe's for some time.  The container does not say anything about being gluten-free, but it also does not say anything about having wheat as an ingredient.  In fact, the only thing it really says is that it is "100 whole grain."  Can I eat the oatmeal?

 

Open Original Shared Link

 

 

gordon

Link to comment
Share on other sites
kareng Grand Master

Oatmeal can be problematic, so I pose this question,.I have been buying John McCann Steel Cut Irish Oatmeal from Trader Joe's for some time.  The container does not say anything about being gluten-free, but it also does not say anything about having wheat as an ingredient.  In fact, the only thing it really says is that it is "100 whole grain."  Can I eat the oatmeal?

 

Open Original Shared Link

 

 

gordon

No.

Oatmeal is an exception. It must say gluten-free. It's just one of those odd things.

However, because a significant percentage of Celiacs react to gluten-free oat, it is recommended that you do not eat them until 6 -12 months gluten-free. Then add them back and see how you do.

Link to comment
Share on other sites
nodrog Newbie

No.

Oatmeal is an exception. It must say gluten-free. It's just one of those odd things.

However, because a significant percentage of Celiacs react to gluten-free oat, it is recommended that you do not eat them until 6 -12 months gluten-free. Then add them back and see how you do.

 

Kareng, thanks again for your advice and comments.  I really appreciate it.  This afternoon I see my gastroenterologist for the first time since I had my blood work, stool samples, x-rays, fluoroscopy. We'll see what, if any, conclusions he might have drawn

 

Thanks, again.

 

 

gordon

Link to comment
Share on other sites
Gemini Experienced

Do not eat the McCann's Oatmeal!  I made that mistake early on and had a pretty good reaction to it.  It is not gluten free...like Quaker Oatmeal.  I do not react to gluten free oats at all but if you buy any that are mainstream and are not from a dedicated facilty/processing, you will probably react to them from cc.

 

As far as the advice from the AMA to wait a long time before trying oatmeal....I didn't.  My gut was totally trashed at diagnosis too.  I waited only 2 months and tried the certified gluten-free oats with great success.  Go figure!  I would say that if you ate oatmeal regularly, like I did, before you were diagnosed, you may not have to wait.  It can be a fiber issue.  Many people do not eat enough fiber in their diets so when they try oatmeal, the fiber causes problems that mimic a gluten reaction.  I love oatmeal and didn't want to wait.

Link to comment
Share on other sites

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,070
    • Most Online (within 30 mins)
      7,748

    TT24
    Newest Member
    TT24
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Fluka66
      Thank you again for your reply and comments which I have read carefully as I appreciate any input at this stage. I'm tending to listen to what my body wants me to do, having been in agony for many years any respite has been welcome and avoiding all wheat and lactose has thankfully brought this.  When in pain before I was seen by a number of gynacologists as I had 22 fibroids and had an operation 13 years ago to shrink them . However the pain remained and intensified to the point over the years where I began passing out. I was in and out of a&e during covid when waiting rooms where empty. My present diet is the only thing that's given me any hope for the future. As I say I had never heard of celiac disease before starting so I guess had this not come up in a conversation I would just have carried on. It was the swollen lymph node that sent me to a boots pharmacist who immediately sent me to a&e where a Dr asked questions prescribed antibiotics and then back to my GP. I'm now waiting for my hospital appointment . Hope this answers your question. I found out more about the disease because I googled something I wouldn't normally do, it did shed light on the disease but I also read some things that this disease can do. On good days I actually hope I haven't got this but on further investigation my mother's side of the family all Celtic have had various problems 're stomach pain my poor grandmother cried in pain as did her sister whilst two of her brother's survived WW2 but died from ulcers put down to stress of fighting.  Wishing you well with your recovery.  Many thanks  
    • knitty kitty
      Welcome to the forum, @Nacina, What supplements is your son taking?
    • knitty kitty
      @BluegrassCeliac, I'm agreeing.  It's a good thing taking magnesium. And B vitamins. Magnesium and Thiamine work together.  If you supplement the B vitamins which include Thiamine, but don't have sufficient magnesium, Thiamine won't work well.  If you take Magnesium, but not Thiamine, magnesium won't work as well by itself. Hydrochlorothiazide HCTZ is a sulfonamide drug, a sulfa drug.  So are proton pump inhibitors PPIs, and SSRIs. High dose Thiamine is used to resolve cytokine storms.  High dose Thiamine was used in patients having cytokine storms in Covid infections.  Magnesium supplementation also improves cytokine storms, and was also used during Covid. How's your Vitamin D? References: Thiamine and magnesium deficiencies: keys to disease https://pubmed.ncbi.nlm.nih.gov/25542071/ Hiding in Plain Sight: Modern Thiamine Deficiency https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533683/ The Effect of a High-Dose Vitamin B Multivitamin Supplement on the Relationship between Brain Metabolism and Blood Biomarkers of Oxidative Stress: A Randomized Control Trial https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316433/ High‐dose Vitamin B6 supplementation reduces anxiety and strengthens visual surround suppression https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9787829/ Repurposing Treatment of Wernicke-Korsakoff Syndrome for Th-17 Cell Immune Storm Syndrome and Neurological Symptoms in COVID-19: Thiamine Efficacy and Safety, In-Vitro Evidence and Pharmacokinetic Profile https://pubmed.ncbi.nlm.nih.gov/33737877/ Higher Intake of Dietary Magnesium Is Inversely Associated With COVID-19 Severity and Symptoms in Hospitalized Patients: A Cross-Sectional Study https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132593/ Magnesium and Vitamin D Deficiency as a Potential Cause of Immune Dysfunction, Cytokine Storm and Disseminated Intravascular Coagulation in covid-19 patients https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7861592/ Sulfonamide Hypersensitivity https://pubmed.ncbi.nlm.nih.gov/31495421/
    • BluegrassCeliac
      Hi,   Not saying Thiamine (B1) couldn't be an issue as well, but Mg was definitely the cause of my problems. It's the only thing that worked. I supplemented with B vitamins, but that didn't change anything, in fact they made me sick. Mg stopped all my muscle pain (HCTZ) within a few months and fixed all the intestinal problems HCTZ caused as well. Mom has an allergy to some sulfa drugs (IgG Celiac too), but I don't think I've ever taken them. Mg boosted my energy as well. It solved a lot of problems. I take 1000mg MgO a day with no problems. I boost absorption with Vitamin D. Some people can't take MgO,  like mom, she takes Mg Glycinate. It's one of those things that someone has try and find the right form for themselves. Everyone's different. Mg deficiency can cause anxiety and is a treatment for it. A pharmacist gave me a list of drugs years ago that cause Mg deficiency: PPIs, H2 bockers, HCTZ, some beta blockers (metoprolol which I've taken -- horrible side effects), some anti-anxiety meds too were on it. I posted because I saw he was an IgG celiac. He's the first one I've seen in 20 years, other than my family. We're rare. All the celiacs I've met are IgA. Finding healthcare is a nightmare. Just trying to help. B  
    • Scott Adams
      It sounds like you've been through a lot with your son's health journey, and it's understandable that you're seeking answers and solutions. Given the complexity of his symptoms and medical history, it might be beneficial to explore a few avenues: Encourage your son to keep a detailed journal of his symptoms, including when they occur, their severity, any triggers or patterns, and how they impact his daily life. This information can be valuable during medical consultations and may help identify correlations or trends. Consider seeking opinions from specialized medical centers or academic hospitals that have multidisciplinary teams specializing in gastrointestinal disorders, especially those related to Celiac disease and Eosinophilic Esophagitis (EOE). These centers often have experts who deal with complex cases and can offer a comprehensive evaluation. Since you've already explored alternative medicine with a nutrition response doctor and a gut detox diet, you may want to consider consulting a functional medicine practitioner. They take a holistic approach to health, looking at underlying causes and imbalances that may contribute to symptoms. Given his low vitamin D levels and other nutritional markers, a thorough nutritional assessment by a registered dietitian or nutritionist specializing in gastrointestinal health could provide insights into any deficiencies or dietary adjustments that might help alleviate symptoms. In addition to routine tests, consider asking about more specialized tests that may not be part of standard screenings. These could include comprehensive stool analyses, food intolerance testing, allergy panels, or advanced imaging studies to assess gut health.
×
×
  • Create New...