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

Myths About Gluten In Everyday Non Edible Objects?


irish daveyboy

Recommended Posts

Lady Eowyn Apprentice

Hi Gemini

My posts always seem to come out wrong!

My DH is caused by ingesting gluten and I get plenty of gastro symptoms!!! What I mean't was no gastro symptoms from the hair products, etc. As you can tell - I'm prone to brain fog too.

My DH is also aggravated by using seasalt on food - sadly. Also have Hashimotos which is affected by iodine too.

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



  • Replies 59
  • Created
  • Last Reply
Gemini Experienced

Hi Gemini

My posts always seem to come out wrong!

My DH is caused by ingesting gluten and I get plenty of gastro symptoms!!! What I mean't was no gastro symptoms from the hair products, etc. As you can tell - I'm prone to brain fog too.

My DH is also aggravated by using seasalt on food - sadly. Also have Hashimotos which is affected by iodine too.

Oh, the brain fog we all understand! :(

I also have Hashi's and that can be difficult from time to time. I have other AI problems also so can understand the difficulty of having all these things going on. I do not have a problem with other food allergies, though, so feel bad you have to deal with all this. The gastro symptoms are bad enough but to have DH on top of that...... :blink:

Do you manage to control your thyroid well? How long have you had Hashi's?

Link to comment
Share on other sites
Lady Eowyn Apprentice

Hi Gemini

Had Hashi's dx at age 15 - that's 36 years ago (aargh!). In hindsight had the celiac from same time and DH very bad when younger from a similar age. Used to get it on shoulder blades, scalp, buttocks and occasionally face - now almost totally confined to scalp. Incredibly symetrical too. Took thyroxine until about 6 years ago when became ill and could no longer take it - a tiny piece of one tablet made me so hyper. Took nothing for 18 months but TSH got to 6.8 and was not well at all. Luckily, found a good doctor who got me on to natural thyroid hormone - raised it slowly and am now fine and dandy on the thyroid front. :rolleyes:. Tried taking iodine some years ago and it made me hypo within 24 hours.

IMHO the celiac and hashi's are hand in hand - for me, gluten seems to affect my thyroid.

Link to comment
Share on other sites
Gemini Experienced

Hi Gemini

Had Hashi's dx at age 15 - that's 36 years ago (aargh!). In hindsight had the celiac from same time and DH very bad when younger from a similar age. Used to get it on shoulder blades, scalp, buttocks and occasionally face - now almost totally confined to scalp. Incredibly symetrical too. Took thyroxine until about 6 years ago when became ill and could no longer take it - a tiny piece of one tablet made me so hyper. Took nothing for 18 months but TSH got to 6.8 and was not well at all. Luckily, found a good doctor who got me on to natural thyroid hormone - raised it slowly and am now fine and dandy on the thyroid front. :rolleyes:. Tried taking iodine some years ago and it made me hypo within 24 hours.

IMHO the celiac and hashi's are hand in hand - for me, gluten seems to affect my thyroid.

Except for the DH, we sound very similar. I've had thyroid issues since I was 17-18 but the idiots I saw at the time had me start thyroid hormone and never did much follow up on it.

I had an enlarged thyroid and no one seemed to think it an issue. I really do not trust specialists at all because of their malpractice. They just blew everything off. I stopped taking it and then when I hit my early 30's, I tanked, big time. I also had Celiac but that wasn't diagnosed until I was 46....the usual story for a Celiac.

I take Nature-throid and it works pretty well but whenever I am really stressed out, I can swing from low to high. That happened this year because I sold my house and moved....twice. Not really a good time! I have read that using iodine can make Hashi's worse in some people. Never tried that because by the time I was diagnosed with Hashi's (a second time), it was really bad and I needed thyoid hormone.

You are 100% correct....the thyroid is the one of the first and most predominant organs attacked in Celiac Disease, after the small intestine. The pancreas is another big autoimmune target and this is why you see so many thyroid problems and diabetes with Celiac. Once you turn on the attack, it doesn't just stop at your small intestine. It's anyone's guess why this is but gluten most assuredly affects my thyroid. Another reason to avoid the stuff..... :ph34r:

I am happy you have a good thyroid doc...I do too. Not an HMO physician and I attribute it to that! ;)

Link to comment
Share on other sites
Lady Eowyn Apprentice

Except for the DH, we sound very similar. I've had thyroid issues since I was 17-18 but the idiots I saw at the time had me start thyroid hormone and never did much follow up on it.

I had an enlarged thyroid and no one seemed to think it an issue. I really do not trust specialists at all because of their malpractice. They just blew everything off. I stopped taking it and then when I hit my early 30's, I tanked, big time. I also had Celiac but that wasn't diagnosed until I was 46....the usual story for a Celiac.

I take Nature-throid and it works pretty well but whenever I am really stressed out, I can swing from low to high. That happened this year because I sold my house and moved....twice. Not really a good time! I have read that using iodine can make Hashi's worse in some people. Never tried that because by the time I was diagnosed with Hashi's (a second time), it was really bad and I needed thyoid hormone.

You are 100% correct....the thyroid is the one of the first and most predominant organs attacked in Celiac Disease, after the small intestine. The pancreas is another big autoimmune target and this is why you see so many thyroid problems and diabetes with Celiac. Once you turn on the attack, it doesn't just stop at your small intestine. It's anyone's guess why this is but gluten most assuredly affects my thyroid. Another reason to avoid the stuff..... :ph34r:

I am happy you have a good thyroid doc...I do too. Not an HMO physician and I attribute it to that! ;)

:)

Hi (might be doing this wrong)!

I take ERFA thyroid and have just ordered Dr Peter Green's book..

Seem to have strayed from the original topic a bit!

Link to comment
Share on other sites
Gemini Experienced

:)

Hi (might be doing this wrong)!

I take ERFA thyroid and have just ordered Dr Peter Green's book..

Seem to have strayed from the original topic a bit!

Excellent book! It gives a great tutorial on how the digestive process works so you really understand how Celiac progresses.

It's a must read if you have Celiac.

Link to comment
Share on other sites
JNBunnie1 Community Regular

Just wanted to chime in here- I personally have a very mild wheat/gluten allergy on top of

the Celiac. I can wash my hands after handling gluten and be just fine, but I realized

while working at a breakfast buffet that some crumbs that had gotten stuck under a large

ring on my finger had caused a small rash to break out after about 8 hours.

I do not think, in general, that when new people are cautioned against personal care

products containing gluten, that it's because there is concern about them having a topical,

allergic reaction. It is simply too easy to stick your fingers, your hair, anything, in your

mouth. I have very long hair and have to tie it up when it's windy or it's constantly whipping

the chapstick/lipstick off my lips and pasting it onto my glasses (very annoying). It also

took me a VERY long time to learn NOT to put my fingers in my mouth. It's just too easy

for the substance of any personal care product to get transferred into someone's mouth,

and I see no reason why anyone should need to take the risk. It's too easy to avoid when

shopping!

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



Gemini Experienced

Just wanted to chime in here- I personally have a very mild wheat/gluten allergy on top of

the Celiac. I can wash my hands after handling gluten and be just fine, but I realized

while working at a breakfast buffet that some crumbs that had gotten stuck under a large

ring on my finger had caused a small rash to break out after about 8 hours.

I do not think, in general, that when new people are cautioned against personal care

products containing gluten, that it's because there is concern about them having a topical,

allergic reaction. It is simply too easy to stick your fingers, your hair, anything, in your

mouth. I have very long hair and have to tie it up when it's windy or it's constantly whipping

the chapstick/lipstick off my lips and pasting it onto my glasses (very annoying). It also

took me a VERY long time to learn NOT to put my fingers in my mouth. It's just too easy

for the substance of any personal care product to get transferred into someone's mouth,

and I see no reason why anyone should need to take the risk. It's too easy to avoid when

shopping!

Actually, I do not find it hard at all to not put my fingers in my mouth, unless I have washed them. I did that long before I was diagnosed with Celiac

and gluten should be the least of anyone's worries on that subject. It's a bad habit to have, especially during cold and flu season. Doorknobs and many

other surfaces are just plain dirty and that's how most people end up sick. I rarely am ever sick and only glutened myself once and that had nothing to do with personal care products.

I think everyone has to look at their personal habits and make their decison based on that. Using personal care products is a choice issue based on habits, not a necessity. My health would never be this good if I were glutening myself on a daily basis.

Link to comment
Share on other sites
IrishHeart Veteran

I do not think, in general, that when new people are cautioned against personal care

products containing gluten, that it's because there is concern about them having a topical,

allergic reaction. It is simply too easy to stick your fingers, your hair, anything, in your

mouth. I have very long hair and have to tie it up when it's windy or it's constantly whipping

the chapstick/lipstick off my lips and pasting it onto my glasses (very annoying). It also

took me a VERY long time to learn NOT to put my fingers in my mouth. It's just too easy

for the substance of any personal care product to get transferred into someone's mouth,

and I see no reason why anyone should need to take the risk. It's too easy to avoid when

shopping!

Sweets, I love ya !

First of all, your topical wheat allergy is a different situation.... but to address your other thoughts?

.The minute amount of "gluten" in diluted shampoo ( i.e. hydrolyzed wheat protein ) also

affecting a "wind-whipped, long haired beauty" (such as yourself) whose hair happens to land in her mouth...

or on her glasses? ...would not really cause a problem for the vast majority of celiacs... Sorry.

You are reaching here ...and I am not even sure how chapstick landing on your glasses fits the discussion.

Honestly, I do not pass the day sticking my fingers in my mouth.

The few times I may lick my fingers is when I am baking and check the batter.

(the other time is when I pose provocatively for photo shoots. :)....)

My hands are clean... usually ...and I wash them after I use the loo or stack wood or pet the cat (but not constantly..... because I am not obsessed with it) and honestly, MOST SOAP BARS AND SHAMPOOS AND LOTIONS DO NOT CONTAIN ENOUGH WHEAT TO CAUSE A PROBLEM.

UNLESS YOU HAVE A WHEAT ALLERGY.

LET'S ALL CONSULT Dr. Green's book or every celiac research center and see that this is the truth.

Link to comment
Share on other sites
JNBunnie1 Community Regular

Well, maybe I'm the only one who ever thoughtlessly stuck their finger in

their mouth to remove a popcorn kernel that was stuck in their gums, or a

piece of roast beef stuck between teeth, or sat down at a restaurant booth

and started eating the chips and guac without washing their hands, or

unexpectedly wound up with a mouthful of hair. (which happens all the time

in my sleep- is it just me? :ph34r: )

That's entirely possible. :D

Link to comment
Share on other sites
IrishHeart Veteran

Well, maybe I'm the only one who ever thoughtlessly stuck their finger in

their mouth to remove a popcorn kernel that was stuck in their gums, or a

piece of roast beef stuck between teeth, or sat down at a restaurant booth

and started eating the chips and guac without washing their hands, or

unexpectedly wound up with a mouthful of hair. (which happens all the time

in my sleep- is it just me? :ph34r: )

That's entirely possible. :D

All of these things are "possible" hunny, but you are assuming your hands already have gluten on them from ?what? exactly??

and I do not see how this is possible. If people wash wash their hands, they REMOVE any trace gluten .

And even when I had long hair, it never ended up in my mouth (unexpectedly or otherwise)

Link to comment
Share on other sites
JNBunnie1 Community Regular

Money, books at the library, door handles, small non-gluten-free children, the grocery store/

shopping cart handles, other peoples pets, generally I sort of do always assume

my hands are covered in gluten... just how my brain works :ph34r:

My only point was that it just seems easier, to me, for someone who is new at this

to relieve themselves of any concern in their personal space when it comes to gluten.

It may not be the most logical, scientific, 'approved' way to go, but don't new people

have enough stress? I like to walk into my house and not worry about anything,

but I realize that's not an option for everyone. I'm really not trying to be contentious.

Link to comment
Share on other sites
IrishHeart Veteran

Money, books at the library, door handles, small non-gluten-free children, the grocery store/

shopping cart handles, other peoples pets, generally I sort of do always assume

my hands are covered in gluten... just how my brain works :ph34r:

That is just the point! New people have enough stress !---and should not worry about

unnecessary "gluten phobias"

Gluten is not "lurking" on books, door handles, children, shopping cart handles or other people's

pets. Germs, maybe but that's another issue.

Unless you are kidding right now and tell us so, frankly, I am a bit surprised at you. :(

Link to comment
Share on other sites
JNBunnie1 Community Regular

You wouldn't be suspicious of money that's changed hands in a bakery? Or the shopping cart

handle that shoppers push around while eating doughnuts? Children covered in Goldfish

crumbs? Don't we recommend that people get gluten-free pet food so their pets don't lick them w/

gluteny tongues? Like I said, it really is ok if it's just me, was only trying to give examples

of how hard it is at first (it was for me anyway, and again it might just be me) to remember

their hands aren't safe. < disclaimer-happy to admit I'm the only one who sees this stuff.

Link to comment
Share on other sites
Darn210 Enthusiast

You wouldn't be suspicious of money that's changed hands in a bakery? Or the shopping cart

handle that shoppers push around while eating doughnuts? Children covered in Goldfish

crumbs? Don't we recommend that people get gluten-free pet food so their pets don't lick them w/

gluteny tongues? Like I said, it really is ok if it's just me, was only trying to give examples

of how hard it is at first (it was for me anyway, and again it might just be me) to remember

their hands aren't safe. < disclaimer-happy to admit I'm the only one who sees this stuff.

Hey Bunnie,

Just wanted to chime in with some support.

Do I think that there is enough gluten in the gluteny shampoos to cause a reaction? . . . Don't know, haven't called any companies to find out what the ppm is.

Do I think having dry hair blown into my mouth once in a while will transfer enough gluten to cause a reaction? . . . Not by itself

Do I think Celiac/NCGI people have to give up their favorite gluteny shampoo? . . . No

Do I think Celiac/NCGI people who use gluteny shampoos need to be diligent? . . . Yes

If I had Celiac, would I use/switch to gluten free shampoo? . . . Yes (there are plenty of mainstream brands to choose from)

Do I think people have their hands to their faces/mouths a lot more than they think they do? . . . Heck Yes . . . and as luck would have it, as I sat back to read what I wrote so far, I put my hand on my chin and my fingers were touching my lips.

I don't have Celiac, but I prepare the majority of my daughter's meals. I constantly tuck my hair behind my ears. I do not wash my hands everytime I do that. Based on my daughter's history, it takes cumulative small exposures to start a significant reaction. I don't know when, where, how much, how often these small exposures take place? I do know, for her, it's cumulative. So doing something like buying Dove Shampoo and Conditioner so that it's one less thing I have to worry about "accumulating" is well worth it to me. I don't look at buying gluten free shampoo as adding stress, I look at it as eliminating it.

And yes, when I had long hair, it occassionally blew into my mouth on a windy day.

Link to comment
Share on other sites
Lady Eowyn Apprentice

Have a nasty feeling that gluten is lurking out there - there's plenty of it about.

If celiac, I think that a good level of caution should be exercised and I would avoid non edible products containing gluten.

I might of course, just be neurotic :blink: .

Link to comment
Share on other sites
jerseyangel Proficient

I don't look at buying gluten free shampoo as adding stress, I look at it as eliminating it.

Ding Ding Ding

I use gluten free personal care products. Personally, when I'm in the shower, I want to shower and not worry about getting shampoo in my mouth as the water runs down my face.

Early on, I was glutened by using a hair gel that contained wheat. (Wasn't diligent enough to wash it all off, I sometimes chew on my nails a bit) No question, and if my hair had been long and blew onto/into my mouth as it does now on occasion, it would have been a direct hit.

When a person new to the gluten free lifestyle asks the controversial topical question, I say do what is best for you. If you can use your gluten containing stuff without issue, go for it. You can always try to eliminate it if you have continuing reactions after you are sure your diet is clean and see if it makes a difference.

Link to comment
Share on other sites
IrishHeart Veteran

Bun,

I do not purchase shampoo, lotion or lipstick with wheat derivatives in it either.

I take precautions like everyone else.

I am not arguing this point.

In fact, you know me well enough to know I am not arguing at all. :)

We have had many conversations and you know I am all about the "what works for you is all that matters" when it comes to anyone

taking charge of her health.

I have always loved this quote from Shroomie, so much so that I bookmarked it:

If every day you followed the health advice for that particular day, you would drive yourself crazy. blink.gif You would be doing what you weren't doing yesterday, and not doing what you were doing yesterday. All you can do is apply a reasoned mind and weigh the balance of the evidence and do what you think is best.

I just know that some people become absurdly gluten-phobic and that makes being a celiac all the more complicated.

IMHO

As for my long hair, it was during the 70's 80's and 90s.. Back then, we used so much gel and hair spray and other junk that perhaps my hair was just too frozen in place to fly in my mouth.

Link to comment
Share on other sites
Gemini Experienced

Money, books at the library, door handles, small non-gluten-free children, the grocery store/

shopping cart handles, other peoples pets, generally I sort of do always assume

my hands are covered in gluten... just how my brain works :ph34r:

My only point was that it just seems easier, to me, for someone who is new at this

to relieve themselves of any concern in their personal space when it comes to gluten.

It may not be the most logical, scientific, 'approved' way to go, but don't new people

have enough stress? I like to walk into my house and not worry about anything,

but I realize that's not an option for everyone. I'm really not trying to be contentious.

I think much of the stress that new Celiacs feel comes from these far out ideas on how one can be potentially glutened.

They are trying to learn the correct way and instilling exaggerated situations that should not be of concern adds to that stress.

If people want to obsess about door knobs, money and library books, that's fine. Good luck with that! :blink:

Link to comment
Share on other sites
GFinDC Veteran

I take Natural Sources Raw Thyroid. It is gluten-free.

Link to comment
Share on other sites
Lady Eowyn Apprentice

If I handle gluten containing products and touch my DH it certainly has an effect - makes it super sore! Had thought this was part of my celiac and didn't realize this was an additional wheat allergy on top. (I don't mean the DH here, but the external wheat product application). If you can understand this you're doing better than me :wacko: .

As for new people, I'm sure they're not dim-wits. It is nice to read different reactions and make up your own mind - not alone in the struggle.

Probably put my foot in it :ph34r: . (Love the smileys - don't know what they all mean).

Take ERFA (natural thyroid hormone).

Link to comment
Share on other sites
jerseyangel Proficient

As for new people, I'm sure they're not dim-wits. It is nice to read different reactions and make up your own mind - not alone in the struggle.

Probably put my foot in it :ph34r:

Not at all, Lady:). I think you summed it up very nicely, and I wholeheartedly agree.

Link to comment
Share on other sites
IrishHeart Veteran

As for new people, I'm sure they're not dim-wits. It is nice to read different reactions and make up your own mind

Not at all!

No one thinks newbies are dim-wits, but gluten- headed people, anxious people, very ill people and scared and new- to- the- diet people---have a lot of questions. You'd be surprised at some of those questions.

Most of us try to give answers that seem reasonable.

I asked a few doozies myself in the beginning and I got panicky at times by what people told me. There is no handbook really, no set- in -stone guidelines and common sense is most definitely needed.

When you first start out, though, it can be very confusing.

Link to comment
Share on other sites
  • 4 weeks later...
danalolly Newbie

Yep.

i have onlyknown i have had celiac for 2 years now, I am 36 years old. I am extremely careful with what i eat so I do not have sttomach issues at all anymorw. only twice duid i get sick by mistake. in the past couple months i have had alot of skin issues, extremely itchy skin everywhere, open sores on my scalp, no relief. i was tested for DH, i dont have. i figured out that the shampoos, hairsprays, and hair dyes had gluten. It has only been 3 days, but my scalp is almost back to normL AND THE ITCHING AND RASHES WENT FROM 100% TO ABOUT 10%. nO DOCTOR TOLD ME THIS, i FIGURED IT OUT, it is frustrating to me that since Ifound out I was celiac, it seems I have to find out what to do all on my own. doctors at times look at me like i am crazy.

another thing weird is that i have had vitiligo ( a skin condition where i do not have pigment in my skin). since I went gluten-free, i have been getting pigment back in my skin. No doctor seems to care about this either. I also had psyoriasis prior to diagnosis, and now it is gone

Link to comment
Share on other sites
  • 1 month later...
JoyMurphy Apprentice

I have severe psoriasis on my scalp. Thus, there are many open wounds on my scalp. I use gluten free hair products. When I am glutened, it affects my hair and my skin as well. I get a wide strip of very coarse hair from the middle of my scalp. My skin becomes thin and easily damaged as well as hyper sensitive. So I have no doubts that inhaling trace amounts or having them seep in, is not safe - at least for me.

I know if I use a hand soap w gluten, it shreds my hands and they dry out and peel like crazy. gluten-free soap doesn't do that.

Not sure about wheat in fabric starch. But after sleeping in a hotel with a heavily starched bed, I had a raging headache. I am very suspicious. Gluten full mascara has the same effect

Not sure if anyone else has the same findings.

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
      121,088
    • Most Online (within 30 mins)
      7,748

    Aventine
    Newest Member
    Aventine
    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

    • Anmol
      Thanks this is helpful. Couple of follow -ups- that critical point till it stays silent is age dependent or dependent on continuing to eat gluten. In other words if she is on gluten-free diet can she stay on silent celiac disease forever?    what are the most cost effective yet efficient test to track the inflammation/antibodies and see if gluten-free is working . 
    • trents
      Welcome to the community forum, @Anmol! There are a number of blood antibody tests that can be administered when diagnosing celiac disease and it is normal that not all of them will be positive. Three out of four that were run for you were positive. It looks pretty conclusive that you have celiac disease. Many physicians will only run the tTG-IGA test so I applaud your doctor for being so thorough. Note, the Immunoglobulin A is not a test for celiac disease per se but a measure of total IGA antibody levels in your blood. If this number is low it can cause false negatives in the individual IGA-based celiac antibody tests. There are many celiacs who are asymptomatic when consuming gluten, at least until damage to the villous lining of the small bowel progresses to a certain critical point. I was one of them. We call them "silent" celiacs".  Unfortunately, being asymptomatic does not equate to no damage being done to the villous lining of the small bowel. No, the fact that your wife is asymptomatic should not be viewed as a license to not practice strict gluten free eating. She is damaging her health by doing so and the continuing high antibody test scores are proof of that. The antibodies are produced by inflammation in the small bowel lining and over time this inflammation destroys the villous lining. Continuing to disregard this will catch up to her. While it may be true that a little gluten does less harm to the villous lining than a lot, why would you even want to tolerate any harm at all to it? Being a "silent" celiac is both a blessing and a curse. It's a blessing in the sense of being able to endure some cross contamination in social settings without embarrassing repercussions. It's a curse in that it slows down the learning curve of avoiding foods where gluten is not an obvious ingredient, yet still may be doing damage to the villous lining of the small bowel. GliadinX is helpful to many celiacs in avoiding illness from cross contamination when eating out but it is not effective when consuming larger amounts of gluten. It was never intended for that purpose. Eating out is the number one sabotager of gluten free eating. You have no control of how food is prepared and handled in restaurant kitchens.  
    • knitty kitty
      Forgot one... https://www.hormonesmatter.com/eosinophilic-esophagitis-sugar-thiamine-sensitive/
    • trents
      Welcome to the forum community, @ekelsay! Yes, your tTG-IGA score is strongly positive for celiac disease. There are other antibody tests that can be run when diagnosing celiac disease but the tTG-IGA is the most popular with physicians because it combines good sensitivity with good specificity, and it is a relatively inexpensive test to perform. The onset of celiac disease can happen at any stage of life and the size of the score is not necessarily an indicator of the progress of the disease. It is likely that you you experienced onset well before you became aware of symptoms. It often takes 10 years or more to get a diagnosis of celiac disease after the first appearance of symptoms. In my case, the first indicator was mildly elevated liver enzymes that resulted in a rejection of my blood donation by the Red Cross at age 37. There was no GI discomfort at that point, at least none that I noticed. Over time, other lab values began to get out of norm, including decreased iron levels. My PCP was at a complete loss to explain any of this. I finally scheduled an appointment with a GI doc because the liver enzymes concerned me and he tested me right away for celiac disease. I was positive and within three months of gluten free eating my liver enzymes were back to normal. That took 13 years since the rejection of my blood donation by the Red Cross. And my story is typical. Toward the end of that period I had developed some occasional diarrhea and oily stool but no major GI distress. Many celiacs do not have classic GI symptoms and are "silent" celiacs. There are around 200 symptoms that have been associated with celiac disease and many or most of them do not involve conscious GI distress. Via an autoimmune process, gluten ingestion triggers inflammation in the villous lining of the small bowel which damages it over time and inhibits the ability of this organ to absorb the vitamins and minerals in the food we ingest. So, that explains why those with celiac disease often suffer iron deficiency anemia, osteoporosis and a host of other vitamin and mineral deficiency related medical issues. The villous lining of the small bowel is where essentially all of our nutrition is absorbed. So, yes, anemia is one of the classic symptoms of celiac disease. One very important thing you need to be aware of is that your PCP may refer you to a GI doc for an endoscopy/biopsy of the small bowel lining to confirm the results of the blood antibody testing. So, you must not begin gluten free eating until that is done or at least you know they are going to diagnose you with celiac disease without it. If you start gluten free eating now there will be healing in the villous lining that will begin to take place which may compromise the results of the biopsy.
    • Anmol
      Hello all- my wife was recently diagnosed with Celiac below are her blood results. We are still absorbing this.  I wanted to seek clarity on few things:  1. Her symptoms aren't extreme. She was asked to go on gluten free diet a couple years ago but she did not completely cut off gluten. Partly because she wasn't seeing extreme symptoms. Only bloating and mild diarrhea after a meal full of gluten.  Does this mean that she is asymptomatic but enormous harm is done with every gram of gluten.? in other words is amount gluten directly correlated with harm on the intestines? or few mg of gluten can be really harmful to the villi  2. Why is she asymptomatic?  3. Is Gliadin X safe to take and effective for Cross -contamination or while going out to eat?  4. Since she is asymptomatic, can we sometimes indulge in a gluten diet? ----------------------------------------------------------------------------------------------- Deamidated Gliadin, IgG - 64 (0-19) units tTG IgA -  >100 (0-3) U/ml tTG IgG - 4   (0-5) Why is this in normal range? Endomysial Antibody - Positive  Immunoglobulin A - 352 (87-352) ------------------------------------------------------------------------------------------------ Thanks for help in advance, really appreciate! 
×
×
  • Create New...