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

Am I Doing Anything Wrong?


Alexolua

Recommended Posts

Alexolua Explorer

Well, been gluten and casien free (hopefully) for 22 days now. I'm not expecting to magically get better all of a sudden, but not really noticing anything yet. So this post is asking if I'm doing anything wrong, and other such things.

Also.. seeing GI Doc again at the end of August, and he doesn't believe I have any problems with gluten. Small Intestines biopsy, was normal. Blood work was inconclusively, and if I'm not feeling any better by the time I see him.. he'll say that shows I don't. Enterolab says different, and just concerned the family support I currently have, might become less, if doctor re-affirms I don't!

And he says Milk isn't a problem either! He claims that since I don't feel the reaction from milk within an hour, I have no problems with casien. I feel it the next day, usually later in the day. I KNOW I react to milk, because it's the same way every time I have milk. Doesn't matter what else I have.. sigh, ranting.

Anyway, me, health wise.. was just a slow, long progression of health worsening since.. like 1993 maybe.. with just some stomach cramping. I think the gluten has just gone after the large intestines, which the GI Doc says isn't possible, of course. Though makes sense with the symptons I have, and with milk affecting me later, since it needs time to get to the more damages area, right?

Okay.. so what I'm doing to aviod gluten, casien.

Got a new pot for cooking, and a pan. It's a non-stick pan. I don't see how that could have gluten in it? I just liked how I didn't need to put anything else in the pan.

Got a new spongue for cleaning too, and keep that and pot and pan seperate.

I haven't gotten any new cups to drink with. Didn't think that was needed, maybe I should get new ones too?

Using the same knife and forks, and spoons (all metal).. didn't buy any new. Maybe that's a mistake?

Though avioding our plates. Using paper ones instead.

I used a bowl once, for a gluten-free cereal and some rice milk, but decided to stop that, since bowls maybe not safe?

Haven't bought any new cooking sheets for the oven, I just put tin foil over them, so any gluten traces on them should be kept off food.

I have had some Lays products they claim to be gluten-free.. though they have that thing on their website saying they could have gluten in them, so think I shouldn't have anymore of that.

Have had some skittles and Starburst, which I've read on here is gluten free.. so that should be safe? Oops if there's casien in them.. argh.

Have had some gluten free products from the store, and I read labels to make sure no dairy.. ugh.. reduces selection.

Maybe it could just take a long while though? Gluten never seemed to cause any real reactions, just worsening health over time. So I don't think even if I was getting traces, I'd know about it. Ugh.. so people real sensitive, lucky in that regard! lol.. sigh.

Answers, comments, anything all welcome. This was part rant, part ask for help! =)


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



Celiac.com Sponsor (A8-M):



gf4life Enthusiast

Hi Alexolua,

Well, there is alot of questions in your post, but I'll try to address a few of them.

First the milk issue. You still might be senstitive to milk, even if your reaction takes a bit longer than an hour. But regardless, you can speed up your gluten recovery time by eliminating all dairy anyhow. So trying gluten and casein free for a while is a good idea. Try for at least two weeks, then add a little bit of milk and if the symptoms return, then you've got your answer. Personally I get a worst stomachache from dairy than I do from gluten, but it goes away sooner. Check all the ingredients of everything you are eating, there is dairy hidden in a lot of foods and not just listed as milk or casein. This also includes whey, sodium caseinate, lactose, and the obvious ones like powdered milk or milk protein. It is not easy being casein free on top of gluten free, but there are so many people out there who do follow the gluten-free/cf diet that you should be able to stick to it pretty well with help.

Starburst and Skittles do NOT have dairy in them. They should be fine.

I think you are doing fine with addressing the cross-contamination issue at home, but make sure you are staying away from all crumbs and such from the counters and tables.

I hope you start feeling better soon. But don't expect you feeling better to get your doctor to support you. It didn't work with mine. She still insists that it is IBS and wants me to eat MORE wheat fiber! I know that I am gluten intolerant and that has to be enough for me right now. My Enterolab results say positive, and that is enough for me. And I do feel so much better being gluten free, and casein free. Just try not to get contaminated too often, that just seems to do me in far too often.

God bless,

Mariann

Alexolua Explorer

Thanks for the reply.

So I shouldn't be scared to use our bowls? Or be better to get new ones? Also with cups, they have had milk in them.. should still be okay, or no? And fork/knives/spoons.. should be safe?

And yeah, I hate whey! LOL.. there were all these gluten free products I found that had whey in them, made me wanna cry!

I think though, it seems gluten free products are much better at labelling if something is containamented.

Though to make matter worse, you could say.. also pretty sure I'm allergic or intorlent to nuts.

So, trying to be casein, nut, and gluten free!

And actually, my doctor has been quite understanding of my wants.. even said if I'm feeling better when I see him, then good! I have been gluten-free/cf for 3 weeks.. unless I messed up somewhere, like with the lays.

Hmm.. think that's all I got for now. Thanks! Oh, and in your opinion, better to stay away from Lays then too? And sorry, this post is question packed too, lol.

Thanks again! =)

Alexolua Explorer

Oh yeah, and to aviod crums and such.. like if I'm putting my spongue down, I put it on a paper towel, so hopefully safe there! Think I'm doing better than when I first started. =)

lovegrov Collaborator

No need to avoid old cups, bowls, plates or silverware.

richard

catfish Apprentice

I think the level of caution is very dependant on the person. I don't eat anything I know or suspect to have gluten in it, but I use the same plates, pots, etc in my house except for wooden spoons which are designated specifically gluten-free or non-gluten-free (and also one for vegetarian food only since we have vegetarian friends). I don't obsess about whether a bowl was once used to hold cookies because that level of paranoia is really bad for my nerves and is likely to add to my symptoms more than 1/100th of a gram of bread crumbs, IMO.

Also, regarding milk- I normally don't get my symptoms from it until the next day (usually the next morning) but they are very definitely milk related and quite severe. I can eat small amounts of dairy with little to no symptoms, but the more I eat the greater the symptoms. Thus I don't obsess about cutting it down to no contamination there either, I just keep tabs on it and don't eat a bowl of ice cream unless I'm prepared to pay for it later. But I might eat a single cheese puff without worrying about it, or put a bit of shredded parmesan on my rice pasta without any concern.

burdee Enthusiast

Alexolua: I've been gluten free (with lotsa slips at first) for 12 weeks and casein free (with one bad slip) for almost 2 weeks. I went casein free after I did a milk free 36 hour test (in anticipation of my Enterolab results). My dramatic reaction to a 1/4 c. 'lactose free' milk convinced me I needed to avoid all dairy even before my E-lab results said gluten and casein antibodies. BTW 'whey protein isolate' in TWO SMALL BITES of a gluten free/lactose free "Protein Fusion" frozen juice bar after a 10 day CF period made me VERY ILL within 24 hours of ingesting that tiny amount. Just as I experienced with gluten avoidance after a short gluten free period, tiny amounts of casein give me terrible reactions. However my casein symptoms differ slightly from my gluten symptoms. Both are very gastrointestinal, but different symptoms help me trace the source of my painful reactions.

I'm sorry to hear you don't tolerate nuts either. I rely on peanut and other nut butters on toast for quick breakfasts, since I don't tolerate soy milk right now. I like PB&J on toast well enough I don't want to try rice or nut milks after doing high fiber gluten cereals and casein filled milk for YEARS to cope with my irregularity symptoms. BTW eliminating the dairy did even more to resolve chronic constipation than eliminating the gluten. CAN YOU TOLERATE SOY? That would give you a great dairy substitution. There are many different varieties and brands of soy milks, yogurts, ice creams, margarine/butter substitutes and even Gluten-free Casein-free dark chocolate bars, if you can tolerate soy.

Have you checked www.gfcfdiet.com which provides dietary intervention support for parents of children with autistic spectrum disorders? They have a great list of 'forbidden' ingredients which contain either gluten or casein. I had just about gotten the list of gluten ingredients memorized when I got my official E-lab casein intolerant diagnosis. So the GFCFDIET website's list has alerted me to all the forms of dairy ingredients hidden in foods.

Feel free to email me to share struggles and/or triumphs with your Gluten-free Casein-free experiences or just keep posting your questions here. Several of us are Gluten-free Casein-free, and maybe others also can't eat nuts. Above all, IT DOES GET BETTER. Yesterday I actually had my FIRST painfree day since starting the gluten-free approach 3 months ago. :D I can't remember how many YEARS I had struggled with abdominal pain before that, but I was given the "IBS" and lactose intolerance MISdiagnoses over 10 years ago. I received that diagnosis after I finally told a doctor about my symptoms which I suffered for MANY years. Going through a day undistracted by abdominal pain was a strange but wonderful experience. I look forward to many more days like that. ;)

BURDEE


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



Celiac.com Sponsor (A8-M):



Alexolua Explorer

Thanks all for responses! =)

catfish -> Yeah, I'm still kinda in crazy mode, a bit.. lol.

burdee:

I'm not sure about Soy, I should just drink a big glass of soy milk to find out, if Soy is bad or not, lol.. though haven't found any soy milk I actually like enough to do that with.

I do have Rice Dream's Rice Drink. Seemed decent.. so, think I'd like to find that ice cream you mention!

Did find a soy margarine though.. which to me seems to taste just like butter! Quite happy with that.

That website, I should go visit too.. kinda haven't been too proactive in looking up CF stuff.. trying to get a handle on the gluten-free part.. was enough at the time, lol.

Hmm.. only question currently I got, is if anyone knows of any brands of potato chips (or junk in general) that are gluten-free without the contamination Lays may have?

I need to go to the store, and write down the phone numbers and such on the products to find out.. but if anyone knows off hand, that'd be easier! LOL

Till later. =)

burdee Enthusiast

Alexolua: I don't think Rice Dream's drink is gluten-free. :o That's why I tried soy milks and then bought some almond milk. Maybe someone else can verify this, but I vaguely recall they used barley in processing that beverage. :unsure:

BURDEE

Alexolua Explorer

Oh shoot! I wasn't even thinking about gluten-free when I got it..

Need to think in terms of gluten-free/CF, both!!

Least I haven't been drinking it that much, like only twice. Didn't enjoy it that much.

  • 1 month later...
BRCoats Enthusiast

I also thought that Rice Dream was gluten-free, but heard that they use barley enzymes. :-( That was a bummer, but I did feel better after eliminating it from my diet. Sorry for the bad news, but hope that helps!!

Brenda

Alexolua Explorer

Thanks Brenda.. and yeah, I got rid of the Rice Dream. Ended up having some of the Rice Dream icecream too, that wasn't dairy free when it claimed so! Ugh.. so, not buying anymore of their stuff. =)

Littlewolf Newbie

Remember to check spices and seasons and read labes for "natural and artifical seasoning" which can contain all that stuff you don't want to eat.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      126,097
    • Most Online (within 30 mins)
      7,748

    John.B
    Newest Member
    John.B
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.2k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • cristiana
      Not sure if related to coeliac disease but my ear ringing  has stepped up a notch since diagnosis.  Even since a child silence really hurts my ears - there is always a really loud noise if there is no other noise in a quiet room - but my brain has learned to filter it out.  Since diagnosis in my forties I also get a metallic ringing in my ears, sometimes just one, sometimes both.  But it comes and goes.   My sister also suffers now, we are both in our fifties, but she is not a coeliac, so for all I know it could just be an age thing.  I do get occasional stabbing pain in my ears but that has been all my life, and I do appear to be vulnerable to outer ear infections too.  So not a particularly helpful reply here, but I suppose what I am trying to say is it might be related but then again it could just be one of those things.   I think in the UK where I live doctors like you to report if you get tinnitus in just the one ear.  I reported mine but no cause was found.  Most of the time it is nothing but sometimes it can have a cause that can be treated, so perhaps worth reporting to your GP.  
    • Scott Adams
      Welcome to the forum, and thank you for sharing your story! It sounds like you’ve been through an incredible journey with your health, and it’s no wonder you’re starting to piece things together and wonder about celiac disease. Your experiences—from childhood through adulthood—paint a picture of symptoms that are often associated with celiac disease, though they can overlap with other conditions as well. The recurring sinus infections, being underweight as a child, chronic gastrointestinal issues, nutrient-related symptoms like cramps, and the persistent fatigue and brain fog are all things that many people with undiagnosed celiac report. Your reactions to gluten also stand out. The improvement in symptoms when you reduce or remove gluten, followed by the resurgence of pain and other problems when you reintroduce it, is a common experience for those with celiac or gluten intolerance. While your frustrations and trials with elimination diets might not have given you concrete answers yet, they’ve provided valuable clues. It’s also worth noting that celiac disease doesn’t always present in the classic way. Many people, like yourself, may not experience severe gastrointestinal distress but instead have “atypical” or extraintestinal symptoms like joint pain, menstrual irregularities, fatigue, and more. It’s a condition that can go undiagnosed for years, especially when symptoms are subtle, sporadic, or mistakenly attributed to other issues. The fact that you’ve sought alternative approaches to feel better shows just how determined you’ve been to find relief, even without a definitive diagnosis. Given your history and how your body responds to gluten, it would be worth exploring celiac disease further with a medical professional. Before removing gluten completely, it’s important to get tested while you’re still eating it, as going gluten-free beforehand can affect the accuracy of the results. A blood test for celiac antibodies (like tTG-IgA) is usually the first step, and if positive, an endoscopy may follow to confirm the diagnosis. If the testing process feels daunting, keep in mind that getting answers could give you clarity and help guide your health decisions going forward. Whatever the outcome, you’ve already made significant strides in identifying triggers and managing your symptoms. Your awareness and persistence are key, and this community is here to support you as you continue to seek answers. This article might be helpful. It breaks down each type of blood test, and what a positive results means in terms of the probability that you might have celiac disease. One test that always needs to be done is the IgA Levels/Deficiency Test (often called "Total IGA") because some people are naturally IGA deficient, and if this is the case, then certain blood tests for celiac disease might be false-negative, and other types of tests need to be done to make an accurate diagnosis. The article includes the "Mayo Clinic Protocol," which is the best overall protocol for results to be ~98% accurate.    
    • More2Learn
      Hi, I am new!  (Although I've used this forum as a reference over the past couple of years.) I'm just looking for some initial reactions to if I actually might possibly have Celiac Disease, or if I'm reaching here.  I have had lifelong health issues and not once has a doctor suggested I look into celiac. I always thought it was basically an extreme allergy that needed an EpiPen, and I know that's not me.  However, I stumbled upon some symptoms, realized I was wrong, and after some research I'm almost shocked at what I have found.  It seems like anything I've ever struggled with has a potential correlation to this disease!  I'm in my 40's, now.  Here is my journey to date... Issues as a Kid: tons of allergies, and had sinus infections all the time... however I didn't have hayfever-like allergies and the scratch tests didn't register much, it was more that when I was exposed to allergens (like say I spent hours with a cat) I was certain to get a sinus infection and it lasted months. was extremely skinny and everyone always said I was anorexic (I wasn't) always getting sick and the illnesses hang on for a long time always cold (my favorite thing to do is sit in front of a space heater or be out in 90 degree weather) intermittent bad constipation (still happens but not as severe) horrible toe cramps that would wake me up in the middle of the night As I got older (teenage/college years): acid reflux diagnosis learned that beer made me EXTREMELY sick, cannot tolerate it horrible issues with menstrual cycle - I wasn't regular, had awful cramps and PMS, sometimes cannot function the first couple of days night terrors/sleep walking more stomach issues - I learned I couldn't have black coffee.  I often had issues especially when traveling.  For example I finally noticed a pattern that I could never, ever eat at a hotel buffet spread - it would always make me sick afterwards. More recent problems: always tired periodic pain on right side that can be so painful I can't stand up straight. Have had all kinds of scans and doctors always say I'm fine.  I was so sure I had gallstones or my liver was failing but... nope. chest pain brain fog not diagnosed but many, many ADHD symptoms lots of inflammation, am overweight now toe cramps evolved into leg/calf cramps None of my symptoms from any era of my life ever really resolved, except I went from being skinny to ~20/30 pounds overweight, and as I got older I got less outright sinus infections.  Largely due to the pain in my right side and the fact that I always, always seem to pick up every illness, especially when traveling, I started pursuing alternative medicine paths... I did the Pritikin lifestyle, I tried an elimination diet, I followed the Root Cause Protocol, I did a Leptin reset.  A lot of these paths recommend removing gluten, and in the past year or so some of my symptoms have gone away!  Specifically less issues with toe cramps, sometimes the side pain would go away for a long time, and my acid reflux got much better.  But, because I was never diagnosed with any specific intolerance, I wasn't militant about the gluten - I had cut out dairy, soy, all kinds of things.  So I would say cross-contamination is ok, or make an exception at a group outing. Then one day, I just got frustrated and ate some normal slices of pizza... and my side pain came back!  I started doing research and now I'm here and wondering... could I have actually had this my whole life??!? Thoughts and observations welcome.           
    • Wheatwacked
      "grass-fed" meat by definition cannot contain wheat as it means the animal is only fed grass  organic meat can be fed wheat feed
    • Scott Adams
      Your symptoms would not be typical celiac disease symptoms, but still could be related due to possible nutrient deficiencies.  The most common nutrient deficiencies associated with celiac disease that may lead to testing for the condition include iron, vitamin D, folate (vitamin B9), vitamin B12, calcium, zinc, and magnesium.  Unfortunately many doctors, including my own doctor at the time, don't do extensive follow up testing for a broad range of nutrient deficiencies, nor recommend that those just diagnosed with celiac disease take a broad spectrum vitamin/mineral supplement, which would greatly benefit most, if not all, newly diagnosed celiacs.      
×
×
  • Create New...