Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

How Do You Cope With This Frustrating Disease


madminx

Recommended Posts

madminx Rookie

Hello everyone,

I was wondering how you all cope with the

incredibly frustrating cycle of celiac disease. I am livid. I got glutened about 3 weeks ago and decided by process of elimination that it was most likely caused by the Absolutely Gluten Free brand flatbread I ate. I was finally starting to feel normal again when last night I began to have symptoms again. Then I found out that it was actually the Simply Organic brand thyme all along that is probably cross contaminated. Now I have to be sick all over again for another 3 to 4 weeks and I am really fed up with this bs. I don't know how to cope with the absurdity of finally feeling well again and then just like that getting sick again from one stupid little mistake.


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



Celiac.com Sponsor (A8-M):



bartfull Rising Star

It is probably NEITHER one that was CC'd. It is probably just that you are still healing and like the rest of us, you will have good days and bad days at the beginning. If you haven't read the newbie 101 thread in the coping section yet, please do. It will help you a lot.

1desperateladysaved Proficient

One must analyze, (as you showed you did) I wouldn't use a product again that I suspected.  Then one must give themselves time to heal.  It can be a rough trip for awhile, but when you head in the right direction, you are bound to get somewhere!  Best wishes for healing.

 

Dee

icelandgirl Proficient

I'm sorry...that is frustrating.  I've been there too.  I do find this disease to be extremely frustrating!

 

How long have you been gluten free?  I think it takes longer to heal than we expect in the beginning.  Do you keep a food diary to figure out when you get symptoms what may have caused it?  I doubt that either of those things would cause a glutening, but that doesn't mean you don't have an intolerance to something else.  It seems like a lot of people on here do.  The food diary might be able to help figure that out.

 

Take care of yourself...I hope you feel better soon.

cyclinglady Grand Master

The crackers look to be just fine. It is a certified gluten-free product. Perhaps you are reacting to one of the ingredients? I had gluten-like issues with Xanthan Gum. It affects me, but not my husband. Go figure!

I am sorry you are not feeling well.

Gemini Experienced

I have had those crackers/flatbread and they are really, really good.  I am a very sensitive Celiac but have been gluten-free almost 10 years so can handle just about anything, food wise.

I have never had any problems with them but they have ingredients that may cause problems for some people....especially if you are new to the diet.  It should not take 3-4 weeks to recover from a glutening so it might just be that you are not healed yet and there are going to be many foods that don't agree with you in the beginning.  It happened to me at first too.

 

Hang in there and I hope you feel better soon! 

moosemalibu Collaborator

I am going to reply on a mental level - as this disease affects us all mentally - and offer that in addition to worrying about the obvious physical symptoms you consider therapy or perhaps meditation. I started therapy and have learned a lot of coping skills instead of  running with my anger, sadness and isolation which was making me a very poor person to be around.


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



Celiac.com Sponsor (A8-M):



madminx Rookie

It is probably NEITHER one that was CC'd. It is probably just that you are still healing and like the rest of us, you will have good days and bad days at the beginning. If you haven't read the newbie 101 thread in the coping section yet, please do. It will help you a lot.

Hello, Thanks for the reply. I know my post is a bit misleading, but I am by no means a newbie. I have been on a gluten-free diet for almost 2 years. This is the first time (and second time last night) I have been glutened in months. 

madminx Rookie

I'm sorry...that is frustrating.  I've been there too.  I do find this disease to be extremely frustrating!

 

How long have you been gluten free?  I think it takes longer to heal than we expect in the beginning.  Do you keep a food diary to figure out when you get symptoms what may have caused it?  I doubt that either of those things would cause a glutening, but that doesn't mean you don't have an intolerance to something else.  It seems like a lot of people on here do.  The food diary might be able to help figure that out.

 

Take care of yourself...I hope you feel better soon.

Hello, thanks for your reply. I've been gluten free for almost 2 years. 3 weeks ago was the first time I got glutened in months (and last night was the second time in months). That's another thing that makes this whole thing so infuriating, I thought I had it all under control and then one little mistake messes it up again. No I don't keep a food diary but I definitely should. 

madminx Rookie

I have had those crackers/flatbread and they are really, really good.  I am a very sensitive Celiac but have been gluten-free almost 10 years so can handle just about anything, food wise.

I have never had any problems with them but they have ingredients that may cause problems for some people....especially if you are new to the diet.  It should not take 3-4 weeks to recover from a glutening so it might just be that you are not healed yet and there are going to be many foods that don't agree with you in the beginning.  It happened to me at first too.

 

Hang in there and I hope you feel better soon! 

Thanks for the reply. Yeah, I don't think it was the crackers. I think it was the thyme. I found a website that says Simply Organic single ingredient spices are not certified gluten free and the company does not guarantee that cross contamination is not present. 

I know my original post is a bit misleading, but I have been gluten free for almost 2 years. 3 weeks was the first time I got glutened in months (and last night was the second time in months). 

madminx Rookie

I am going to reply on a mental level - as this disease affects us all mentally - and offer that in addition to worrying about the obvious physical symptoms you consider therapy or perhaps meditation. I started therapy and have learned a lot of coping skills instead of  running with my anger, sadness and isolation which was making me a very poor person to be around.

Thanks for your reply. I was in therapy a few months ago, and my therapist didn't believe that I had celiac. Mainly because it was not diagnosed by a doctor. It was hard that not even my therapist believed me (along with a bunch of friends). I eventually did get tested by a doctor but it came out negative because I had been on the gluten free diet for about a year at that point. I did learn a few good skills but I think it would have been more effective if my therapist believed me. 

moosemalibu Collaborator

Thanks for your reply. I was in therapy a few months ago, and my therapist didn't believe that I had celiac. Mainly because it was not diagnosed by a doctor. It was hard that not even my therapist believed me (along with a bunch of friends). I eventually did get tested by a doctor but it came out negative because I had been on the gluten free diet for about a year at that point. I did learn a few good skills but I think it would have been more effective if my therapist believed me. 

 

I'm sad to read that your therapist did not believe you. Did they ask you if you were officially diagnosed? I honestly would find a new therapist, tell them you have the disease and then if they ask if you were diagnosed you tell them yes. None of their business whether you got a traditional diagnosis or not. Their job is to help you cope. Ugh that is so frustrating. ::hugs::

icelandgirl Proficient

Hello, thanks for your reply. I've been gluten free for almost 2 years. 3 weeks ago was the first time I got glutened in months (and last night was the second time in months). That's another thing that makes this whole thing so infuriating, I thought I had it all under control and then one little mistake messes it up again. No I don't keep a food diary but I definitely should.

The food diary helped me to see that I can't handle a lot of fat...probably the result of no gallbladder...it was removed 2 weeks after celiac diagnosis. I was still having issues with bloating and D and so have been cutting out other things trying to figure out some more. It may help you to figure out some other things that may bother your system.

Mentally...coming on here and venting helps...I feel less alone in it when I do. But it is no doubt a frustrating disease...I think especially because all I was told by my Dr was don't eat gluten. Seems like it takes more than that for a lot of us.

madminx Rookie

I'm sad to read that your therapist did not believe you. Did they ask you if you were officially diagnosed? I honestly would find a new therapist, tell them you have the disease and then if they ask if you were diagnosed you tell them yes. None of their business whether you got a traditional diagnosis or not. Their job is to help you cope. Ugh that is so frustrating. ::hugs::

Yes he asked and i told him I was not officially diagnosed. Good idea! That's what I'll do when I get a new therapist. That way I can get some actual therapy and not just another person who doubts me. Thanks /hug. It really is frustrating. I'm glad this forum is here to get support from others who know how it is. 

madminx Rookie

The food diary helped me to see that I can't handle a lot of fat...probably the result of no gallbladder...it was removed 2 weeks after celiac diagnosis. I was still having issues with bloating and D and so have been cutting out other things trying to figure out some more. It may help you to figure out some other things that may bother your system.

Mentally...coming on here and venting helps...I feel less alone in it when I do. But it is no doubt a frustrating disease...I think especially because all I was told by my Dr was don't eat gluten. Seems like it takes more than that for a lot of us.

I think I have IBS on top of the celiac disease, or it's just my body still trying to heal from the damage the gluten has done. I can't handle a lot of fat either, and I have stomach issues when I get stressed out. It doesn't take much. I will definitely start a food diary. 

 

Yes it definitely helps to vent. I'm glad this forum is here to talk to people who actually get it. Thanks for your support. 

frieze Community Regular

if you can't digest well, perhaps some enzyme therapy is in order.

moosemalibu Collaborator

if you can't digest well, perhaps some enzyme therapy is in order.

I second digestive enzymes. They can be helpful. Have your stool checked by your doctor for fat as excessive fat can indicate a pancreatic disorder. Some Celiacs have pancreatic insufficiency secondary to celiac disease and it takes some gut healing to have it resolve and they are put on additional enzyme therapy (I believe... not 100% certain on it).

Gemini Experienced

You don't have to go to a doctor to be tested for insufficiency.  If you have a problem digesting fats, you will know it.  I always suggest taking OTC digestive enzymes because they help tremendously.  I have been gluten-free almost a decade and this year, stopped using them to see what would happen.  I was using them far less frequently than when first diagnosed.  Low and behold.......I don't need them anymore.  I am eating more foods than ever, a completely normal diet and everything goes through as it should, with no more issues eating fats!  This particular problem takes quite awhile to correct as fats as just so hard to digest.

dilettantesteph Collaborator

I agree with others about the digestive enzymes.   I had diarrhea with high fat meals which resolved with the enzymes.

 

Tricia Thompson did a report on gluten contamination of spices: Open Original Shared Link

I couldn't get it to load, but maybe you can and maybe it'll be helpful.

 

I remember coming on here after reacting to things and trying to figure out what was going on.  People kept telling me it was something else because they ate that thing just fine.  Then my GI doctor told me that some celiacs are more sensitive to trace contamination than others. 

 

You can read the studies for yourself:

Open Original Shared Link

"After a baseline evaluation (t0), patients were assigned to ingest daily for 90 d a capsule containing 0, 10, or 50 mg gluten."

"One patient (challenged with 10 mg gluten) developed a clinical relapse."

The others did not.  Less than 10 mg of gluten has been defined as safe for the vast majority of celiacs.

 

Open Original Shared Link

"The study by Catassi et al also implies that minor gluten contamination was not harmful to most of the patients."

"As the study by Catassi et al (Open Original Shared Link) showed, celiac disease patients respond individually to small amounts of gluten. The individual variability denotes that the treatment should be individual too."

 

Some individuals experiencing symptoms on the gluten-free diet responded to a trace gluten contamination elimination diet: Open Original Shared Link

 

The good news about that is this: "Most patients who respond to a 3-6 month course of the GCED are subsequently able to return to a traditional GFD without return of symptoms."

 

I am hoping that will work for me too.  I just got glutened by accident so I'm back to day one of my 3-6 month course.

 

 

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,957
    • Most Online (within 30 mins)
      7,748

    Dogdad21
    Newest Member
    Dogdad21
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.