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 Our Content
    eNewsletter
    Donate

New And With Questions..


Bekka

Recommended Posts

Bekka Newbie

Hey everyone. I'm new here, and new to gluten-free.

Right now, I am in the process of practicing a gluten-free lifestyle as to figure out whether or not I am gluten intolerant. I have no health insurance and no money outside of what I make to pay for bills and living expenses (I'm a broke 25 year old, ha) so I don't really have means to get a test done for Celiac disease. Gluten intolerance has been suggested to me in the past by doctors, but I blew it off because I was an ignorant kid and "didn't care". Recently, because I am in therapy for an ongoing eating disorder, it was suggested to me again, because we were discussing my body image. I explained to my therapist that my body image issues had much to do with how I physically felt, and I've been telling therapists and doctors this for YEARS--- you don't feel like you look that great, when you feel like hell-- and you especially don't feel good about eating when everytime you eat, you feel worse. We made the connection that the foods that seemed to make me feel even worse were foods that contained gluten.

Now, I don't know how probable this is. I really don't know a whole lot about the intolerance/disease and the differences between gluten intolerance and Celiac---I know that Celiac is an autoimmune disease...BUT, do the symptoms differ as well?

I took it upon myself to go gluten-free to see if I noticed any changes. I'm aware it can take a long time to notice differences, however in the past week, I have already noticed drastic changes in my gut. I don't feel weighted down and have irritable bowels as much. It's not perfect yet, as I suspect it's going to take a long time for me to feel "normal" if I am gluten intolerant, but it's a LOT better already.

I guess my main question though is if the symptoms for Celiac differ from those of an intolerance? I ask because I am not sure how far to take this. As far as eating goes I have been eating things that I know are gluten-free (well, to the best of anyone's knowledge, that is) but don't know how important it is to switch shampoos, etc?

I know that there are different levels of sensitivity for people. I live with a boyfriend who is far from gluten-free, and don't want to make him feel obligated to change his way of living, either.

Most of my symptoms are gastrointestinal, but I've also been struggling a lot with anxiety. I also have Raynaud's which sort of came out of nowhere when I was about 20 years old. I am considering whether or not this might be linked? And if so, can something like that be linked with a gluten intolerance, or is it more likely to be linked to Celiac because of the autoimmune aspect? I'm sort of lost. (I also struggle with a host of other symptoms that can be linked to a gluten intolerance/Celiac, much dealing with mental--i.e. foggy brain, fatigue, mood swings, etc.-- and hormonal, as well as skin rashes, the gastrointestinal stuff, etc.)

I'm meeting with a nutritionist on Friday to get things underway and some ideas (free of charge) so I'm hoping to get some answers then, too.

I am just wondering how all of you have determined how sensitive you are? Is it through testing or by observation? I know I should get the test done but simply don't have the money :/ Ideas???


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



Celiac.com Sponsor (A8-M):



mommida Enthusiast

I think everyone finds out that your reaction is an individual experience. It does seem that quite a few people feel reactions to accidental gluten exposure after being gluten free is more severe.

Symptoms of Celiac and gluten intolerance are quite a long and varied list. This has lead to many misdiagnoses for some people.

It might be helpful to keep a food journal. You can track your progress, identify other food intolerances, cross-contamination exposures, and in general just take out a lot of guess work.

Welcome to the board! There are many people willing to help with advice from their own personal experiences and support and understanding the changes you are going through. :)

Kjas Newbie

It certainly sounds like you are gluten intolerant or have celiac disease.

Raynaud's alone is inherently linked to the autoimmune system, so at a guess and along with you other symptoms I would say it's likely. Celiac disease and gluten intolerance aren't really separate things per say, its more of a spectrum. At the moment, we really don't know all there is to know about either of these conditions (barely scratched the surface actually), to the extent that many doctors, particularly GP's believe that the neurological symptoms have nothing to do with the either condition (many of us who live with it know that's incorrect). Testing can be useful but even that is somewhat flawed, as they have a 30% rate of false negatives.

As for how sensitive you are, it's just a learning curve really. When you stop reacting to obvious things, you may start reacting to the less obvious ones. The sensitivity is almost always from observation. It can take a year or so to really get the hang of it, and particularly during the first 3 months, you will probably have quite a few accidents and that's normal. If you get stuck on something or can't figure something out, most here are happy to help with answering any questions, but most of the time it's going to be trial and error.

Bekka Newbie

thanks guys, for your help and ideas. I am seriously considering getting a quote on how much it would cost out of pocket to get the testing done-- has anyone without insurance done it?

I've read that in order for the test to be as accurate as it can be though, that you can't be eating gluten-free before the test?

The thing that works to my advantage I think is that I've always been sort of hyper-aware of physical sensations and the way my body reacts to things, so I shouldn't have too much trouble recording my observations. I have to say though, it's amazing to me that I haven't had really any tummy trouble for the week that I've been eating gluten free...I can't even remember a time (at least not before the age of 10) that I didn't have a stomach ache for even a day or two. I did go raw-vegan/fruitarian at one point a couple years ago and also noticed a huge difference, but I still struggled with stomach issues because I am pretty certain I also have trouble with nuts. I was eating a lot of raw cashews (making "raw sauces" and stuff out of them) and I found that nuts really screwed my gut up, but at the time it was my only source of protein. I found that on days, though, where I didn't consume nuts, my gut felt pretty darn close to a million bucks...and my hair grew like crazy, too! Raynauds was almost non-existent, and mentally I felt a lot clearer than I have in yeears. Raw-vegan was way too hard to keep up with though, and I ended up gorging on junk when I switched back to a more "normal" way of eating, and then all the other problems began again. Sigh.

researchmomma Contributor

Welcome to the Board. My daughter is non-celiac gluten intolerant. We are seeing that she has malabsorption issues much like Celiac because she has high fecal fat (but we are hoping to rule out some other diseases like Crohn's Dissease too). However, we know she is very sensitive to gluten. So I feel the big difference between gluten intolerance and Celiac is the intestinal villous blunting which is diagnosed by biopsy.

I replied to answer your question about testing. Yes, you have to be eating gluten for them to work. Since you have only been gluten-free for one week, you could start eating it again and get the blood test in a week or two I suppose (someone more medically savvy will reply).

The cost of the blood work is about 200 dollars. We did ours without a doctor through www.ineedlabs.com. However, there is a 30% (at least) false negative. But if you really want to get the blood work done (I did) before you go completely gluten free, do it now because after you are gluten-free for a period of time, it is very hard to go back. My daughter was accidentally glutened after being gluten-free for 3 weeks and she got very sick (all the old symptoms came back with a vengeance). If her doctor asked her to eat gluten again, I am not sure we could do it. Her anxiety, moodiness and gut reactions are not worth eating eat.

If you decide to do the labs from ineedlabs.com, you will want the Comprehensive Celiac Panel, not the HLA gene test if you are trying to save money.

It sure sounds like you have Celiac with that Reynaud's diagnosis. Eating gluten free can be overwhelming in the beginning but this board is a fabulous resource so ask away. My daughter is only frustrated by gluten free if her friends are hanging and eating pizza or some other easy to grab food that she can't have. However, I then remind her that she didn't like pizza because it made her stomach hurt, etc. We laugh then. It is more about being told you can't have something than it is about eating gluten free. Hope that makes sense.

Welcome to the road of better health.

Bekka Newbie

Welcome to the Board. My daughter is non-celiac gluten intolerant. We are seeing that she has malabsorption issues much like Celiac because she has high fecal fat (but we are hoping to rule out some other diseases like Crohn's Dissease too). However, we know she is very sensitive to gluten. So I feel the big difference between gluten intolerance and Celiac is the intestinal villous blunting which is diagnosed by biopsy.

I replied to answer your question about testing. Yes, you have to be eating gluten for them to work. Since you have only been gluten-free for one week, you could start eating it again and get the blood test in a week or two I suppose (someone more medically savvy will reply).

The cost of the blood work is about 200 dollars. We did ours without a doctor through www.ineedlabs.com. However, there is a 30% (at least) false negative. But if you really want to get the blood work done (I did) before you go completely gluten free, do it now because after you are gluten-free for a period of time, it is very hard to go back. My daughter was accidentally glutened after being gluten-free for 3 weeks and she got very sick (all the old symptoms came back with a vengeance). If her doctor asked her to eat gluten again, I am not sure we could do it. Her anxiety, moodiness and gut reactions are not worth eating eat.

If you decide to do the labs from ineedlabs.com, you will want the Comprehensive Celiac Panel, not the HLA gene test if you are trying to save money.

It sure sounds like you have Celiac with that Reynaud's diagnosis. Eating gluten free can be overwhelming in the beginning but this board is a fabulous resource so ask away. My daughter is only frustrated by gluten free if her friends are hanging and eating pizza or some other easy to grab food that she can't have. However, I then remind her that she didn't like pizza because it made her stomach hurt, etc. We laugh then. It is more about being told you can't have something than it is about eating gluten free. Hope that makes sense.

Welcome to the road of better health.

Sigh, $200? That's not something I can afford anytime soon unfortunately :(

So, I guess my next question is. If I were to take the safe route of just assuming I may have Celiac just to err on the safe side of things-- would it be required to switch all hair products, body soaps, laundry detergents, and other things that only make contact with the skin and are not ingested? Or is this suggested because there's the assumption you will put your hands in your mouth?

What seems the most overwhelming to me, isn't even what I can't have, it's the expense of the gluten-free alternatives to get the feeling that I'm still eating foods I enjoy/other products I enjoy. I guess that would be another question... what are some strategies for living gluten free on a budget? I've read about baking your own gluten-free breads and such. Breads aren't a huge concern to me, pasta is more likely to be a point of weakness for me. And as for the hair/skin products, are there more generic, name-brand products that are gluten free so that I don't have to spend a fortune? (links to other topics about similar things or websites are cool, since I'm sure all of this has been asked at some point)

Today I have to get some new foundation makeup (clumsy and broke my bottle of it this morning) and wondering if any of the cheaper big brands carry any that are gluten free? I was using Cover Girl, but I have no idea where to start in finding out what to watch out for. I have a list of ingredients that aren't safe... but is that all I need? It seems like there can be so many different complications with cross-contaminations or mislabeling. Bah.

I do pretty well with eating gluten-free because a lot of my favorite foods are relatively simple, and I'm used to restrictive diets from being vegan for 8 years, etc. I worry more about everything else that goes into it, the skin products, the worry about CC, etc.

Another thing is trying to help my boyfriend (I live with him) understand all of this. He's super supportive and trying to learn about it but because I don't even know the ins and outs of all of it, (and I'm sure even those who have been gluten-free for years still learn things) I don't totally know how to help him understand and he's not much of a reader :P

Thanks again everyone. Very much appreciate the replies! <3

researchmomma Contributor

You can definitely go gluten free without testing but if you want to know if you are Celiac you need the testing. Is there any State or Federal programs that you would qualify for? Probably not, but thought I should ask.

I am no expert on skin care products but someone posted here that gluten is a large molecule and doesn't cross the skin barrier. Honestly, I would wait for awhile to worry about that. Start eliminating the WADS of gluten that you are ingesting. I will let others comment on that.

Do you have a Trader Joe's near you? Their rice pasta is pretty darn good and dang cheap. I have one indulgence....I cook trader joe's spiral rice pasta (they have a huge list of gluten free products including cosmetics) and I use the Kraft Mac and Cheese packet which is gluten free. I cook the pasta, set it aside, then mix the cheese packet with the butter and milk until smooth and then I toss the pasta in. Cheap and good. If you like canned chicken or tuna you can toss that in. My daughter is so happy I can make that for her.

I am sure if you start feeling better, you boyfriend will be on board. My husband thought "wow, so much work" until he witnessed how much her health improved.


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



Celiac.com Sponsor (A8-M):



Melissa Palomo Apprentice

My opinion isn't always the popular one - but if you feel better gluten-free and don't have the means to easily get tested - then just live a gluten-free life. There's not anything I do differently than my gluten intolerant friends - we both live a gluten free lifestyle. And we both feel like crap when we eat gluten. Sure, it puts you at a higher risk for certain things later in life but not much you can do about it now.

If you later have the means to get tested, go back on gluten and do it - but IMO the goal should be to do what you have to do to feel better whether you have a Celiac diagnosis or not.

Bekka Newbie

researchmomma,

I may qualify actually, because I did in the past when I sprained my ankle...I'll have to check it out.

As for the skin products, I checked out what I use anyway, and I am pretty sure the stuff I use is gluten free--not sure about CC, but the ingredients themselves seem to check out just fine.

I tried some sort of rice pasta the other day with pesto, it was darn good! Didn't notice much of a difference besides the noodles seemed softer/flimsier, and I'm okay with that because I always overcooked noodles to get them mushy-soft. I have been eating a LOT of low-sodium/gluten free canned tuna and salmon on Udi's bread with that Smart Balance gluten free mayo spread...soo good.

I was laying in bed last night thinking, realizing that I wasn't going to bed with a gurgly, crampy, upset stomach--that alone is worth the gluten-free lifestyle to me. Whether or not I have a problem, I can already see I feel better...digest gluten-free foods much better.

Another question though...I read about teeth and gum problems if you're gluten intolerant/celiac-- when some of you switched to gluten-free did you notice your gums becoming more sensitive at first? The past couple days when I brush my gums bleed like crazy and they never did before? I've had gingivitis for quite some time but never had a big problem with it before.

And Melissa, I like your way of looking at it. Like I said the lack of stomach problems alone is worth it to me.

Thanks guys! :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      129,966
    • Most Online (within 30 mins)
      7,748

    Susan Allsopp
    Newest Member
    Susan Allsopp
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Wheatwacked
      Hello @CeliacNew, If you are Vegan to help you feel better, reconsider returning to omnivore.  Actually, since you are already on a very restrictive diet, transitioning to gluten free might be easier for you.  Read the ingredient labels, Particularly vitamin D and Choline require supplements for vegan diet because our primary source is sun, eggs and beef.  B12 also.
    • Wheatwacked
      Once you've completed testing and still don't have improvement, start a trial gluten free diet.  Looking for imprvement that may indicate Non Celiac Gluten Sensitivity, which is 10 times more prevalent than Celiac Disease. Deficiencies in vitamins B6, B12, D, and C can manifest as skin rashes.  Virtual guaranty you are deficient in vitamin D.
    • cameo674
      So those rs numbers tell researchers where the dbSNP is located in a Genome so that other reasearchers or an AI system can look in that specific spot for that Snip of information.  You can look those rs # s by pasting the numbers after rs into the lookup on this page https://www.ncbi.nlm.nih.gov/snp/ right under the Blue header bar at the top of the webpage.  Since you are not a researcher, I do not know how this will help you though.
    • cameo674
      So I posted here once before, and everyone advocated that I get into a GI doc.  I finally got into my functional health appointment on 6/16 to get my blood results evaluated and get the Gastro referral. I was told that I would be fortunate to see a gastro doctor by December, because of the number of people waiting to get in, but they did believe that I needed to see a GI doc among others.  Well, the stars aligned. I got home. I looked at MyChart and it showed an appointment available for later that same day. I never clicked so fast on an appointment time. The gastro doc ran some additional blood work based off the December values that had confirmed my daughter's suspicion that I have undiagnosed stomach issues.  Gastro has also scheduled me to get an upper endoscopy as well as a colonoscopy since it has been 8 years since my last one. She said it would rule out other concerns if I did not show Celiac per the biopsies.  Those biopsies will not occur until August 29th and like everyone here stated, Gastro wants me to keep gluten in my diet exactly as everyone suggested. To be honest, I was barely eating any gluten since I figured I would have plenty of time to do so before testing.  Doc is also looking for the cause of the low level heartburn that I have had for 30 years.  I have mentioned the heartburn to PCPs in the past and they always said take a tums or other OTC drug.  The upper endoscopy is for ruling out eosinphilic esophagitis, h. pylori, and to biopsy the duodenal bulb and second portion to confirm or exclude celiac. The colonoscopy will have random biopsies to rule out microscopic colitis. I didn't really catch her reasoning for the bloodwork.  Doc looked at the December numbers and said they were definitely concerning for Celiac.  She also said, “Hmm that’s odd; usually it’s the reverse”, but I did not catch which result made her say that. She seems very through.  She also asked why I had never bothered to see a GI before.  To be honest, I told her I just assumed that the heartburn and loose stool were a part of aging.  I have been gassy since I was born and thought constantly passing gas was normal?  Everyone I know with Celiac have horrible symptoms that cannot be attributed to other things.  They are in a lot of stomach pain.  I do not go through that.  I attribute my issues to the lactose intolerance that comes with aging, but have slowly been eliminating foods from my diet due to the heartburn or due my assumption that they did not agree with a medication that I was prescribed. I have already eliminated milk products especially high fat ones like ice cream; fats like peanut butter; acids like citrus and tomatoes; chocolate in all forms; and breads more because it is so hard to get in 100 grams of protein if I eat any foods that are not a protein.  I would not have even done the testing if my daughter had not brought up the fact that she thought I might have an undiagnosed condition since she has issues with bloating and another sibling has periodic undiagnosed stomach pain that GI docs throw pills at instead of helping.  Who knew that Bristol scale 5 and 6 were not considered normal especially multiple times a day? I watched my MIL go through basically the same bowel changes starting at 50 so to be honest, I really did think it was normal before this week's appointment.   December 2024's blood tests ran through Quest Labs were:  Deamidated Gliadin (IgA) 53.8 U/mL Above range >15.0 U/mL; Deamidated Gliadin (IgG) >250.0 U/mL Above Range >15.0 U/mL; Tissue Transglutaminase (IgA) 44.0 U/mL Above range >15.0 U/mL; Tissue Transglutaminase (IgG) <1.0 In range <15.0; Immunoglobulin A (IgA) 274 mg/dL In range 47-310 mg/dL 6/16/25 bloodwork:  Until today, I did not really know what all the four tubes of blood were for and since I did not understand the results, I got into the clinical notes to see what was ordered, but it did not exactly explain why for everything. Immunoglobulins IGG, IGA, IGM all came back in range:  IGG 1,010 mg/dL In range 600-1,714; IgA 261 mg/dL In range 66-433 mg/dL; IGM 189 mg/dL In range 45-281.  How do these numbers help with diagnosis? Google says she checked these to see if I have an ongoing infection? I do have Hashimoto's and she did say once you have one autoimmune disease others seem to follow. Celiac Associated HLD-DQ Typing: DQA1* Value: 05; DQA1*DQA11 Value: 05; DQB1* Value: 02; DQB1-DQB11 Value: 02; Celiac Gene Pairs Present Value: Yes; Celiac HLA Interpretation Value: These genes are permissive for celiac disease.  However, these genes can also be present in the normal population. Testing performed by SSOP.  So google failed me.  I think these results basically say I have genes, but everybody has these genes so this test was just to confirm that there is a vague possibility?  Maybe this test result explains why I do not have the horrible symptoms most individuals with celiac have?  I told the GI my assumption is that I am just gluten intolerant since I do not have the pain? So maybe this test explains why I have antibodies? Comprehensive Metabolic Panel: Everything was in the middle of the normal range.  Google says this just says I am metabolically healthy. Tissue Transglutaminase ABS test results – Done by the Mayo Clinic’s Labs –  T-Transglutaminase IGA AB --Value: 3.1 U/mL – Normal Value is <4.0 (negative) U/mL; Tissue Transglutaminase, IgG -- Value: 15.3 U/mL High -- Normal Value is <6.0 (Negative) U/mL – Interpretation Positive (>9.0) – These are the only labs the GI did that have been labeled Abnormal.  I am confused at how/why these came back different than the December labs? Because these numbers seem to be the opposite of what the were in December and I know I have eaten less gluten.  They were definitely measured differently and had different ranges. This must be why she said they are usually opposite? Molecular Stool Parasite Panel said I was Negative for Giardia Lamblia by PCR; Entamoeba Histolytica by PCR and Cryptosporidium Parvum/Hominis by PCR.  So at least I do not need to do a parasite cleanse like everyone on TikTok seems to be doing. So I guess, I am just really asking why the Tissue Transglutaminase numbers are different.  Was it because they were truly different tests? Is it because I have not consumed the crazy amount of gluten one is suppose to eat prior to testing? To be honest, I thought that was only for the biopsy testing. I generally only eat twice a day, and the thought of eating the equivalent of 6 slices of bread is daunting. Even in my youth, I probably only consumed the equivalent of maybe 3 slices a day. Like I said before, now I usually focus on trying to eat 60 gram of protein.  I am suppose to consume 100 grams, but have failed to succeed. I will focus on eating gluten starting in July now that I know my procedure date.
    • Scott Adams
      I agree with @trents and wiping down the spot you eat your lunch, and eating the food your brought from home should be safe for even sensitive celiacs. Gluten can jump on your food, so it would likely better better for you to continue eating where you prefer.
×
×
  • Create New...