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

Still Devistated


MelissaSH4

Recommended Posts

MelissaSH4 Newbie

I was diagnosed in October 2011 after 3 weeks of severe, intense, mind boggling, crippling abdominal pain. That along with a terrible mind fog, however, was my only symptom. Not the classic Celiac case by any means, and although my husband later confessed that he felt like he was watching me die (I was on a "bland" diet while they tried to figure out what was wrong with me bland being consistent of crackers and chicken noodle soup go figure!) and I guess in a way I was slowly poisoning myself. When I got the phone call from the DR I was so relieved that there was an answer really didn't care what was wrong I finally knew how to feel better. So here I am, almost a year later, and yesterday I called my GI specialist to see if there was ANY possibility that I was misdiagnosed! I have been CC'd a few times and the flare only lasted a day or two so I guess I should consider myself lucky but in reality I feel like a broken freak. I just want to be normal! So I guess my real question is when do I get over the emotional aspect of this disease? Technically the diet isn't difficult to follow...read your labels and know what is in your food. I think that part of my struggle is the fact that I NEVER cheat so when I flare it


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



Celiac.com Sponsor (A8-M):



justlisa Apprentice

Hi Melissa...

I am not sure that I can be much help to you...but, I am going to try...

To me, it's not feeling like a freak...it's normal... And, I have a hard time relating to the feeling of "being deprived" and the urge to "cheat" that I read, so often, in here. Please, don't take that to mean that I don't empathize...I totally do! It's just that I don't feel those things. I've actually thought a lot about "why" I don't...

For me, it's simply this:

Gluten is poison...for me and many, many others... Why "feel deprived" about not being able to have "poison"? I equate it to going out to the garage and opening up a jar/can/bottle and taking a big ol' swig...

"Antifreeze" is toxic...deadly, in fact. We, humans know not to drink it...nor do we want to. But, animals think it sweet and tasty! Which is why we humans have to keep dogs/cats/etc away from it (make sure we rinse off that big puddle from the driveway, etc). I, also, know that grapes and chocolate (to name a couple) are toxic to my dogs so, I make sure they don't get access to the stuff... I don't feel sad for them, though. I know it's for the best...

"Cheating"? Same thing...it's POISON. I don't, honestly, care that others get to have "it". In fact, I feel sorry for them (I don't think gluten is "good" for anybody...just my perspective).

Perhaps if you can, really, come to the understanding of just how "deadly" (and, yes, gluten is "deadly" to the celiac/gluten intolerant) it is to you, it won't be such an emotional struggle?

I know this might sound simplistic...it's just how I feel...

Last, but very important, if you continue to feel this way, don't hesitate to get some help... Maybe a therapist could help you sort through it all?

I hope you can find peace so you can move forward...happily and in good health.

:)

GFinDC Veteran

Hi,

It sounds like you had pretty severe symptoms before you were diagnosed and went on the gluten-free diet. Any negative reaction to eating gluten is a sign that you shouldn't be eating it. Your body isn't playing games or trying to fool you if it starts reacting. You may not have severe reactions right away but most likely you would develop them over time if you went back on the gluten eating way. Damage can build up and get worse and worse. And spread to other parts of the body besides the gut. People die from celiac disease. Some people have no symptoms at all and they are termed "silent celiacs". Probably most of them are not diagnosed and walk around eating gluten thinking everything is fine. Which is sad because they will certainly develop problems over time if they are unable to absorb vitamins or the inflammation causes cancer in their gut, or some other autoimmune disease develops.

You said you improved going gluten-free right? Why do you think that is? Is it because you didn't eat gluten or was your doctor wrong? I don't see how you doctor could have been wrong about celiac if you improved though.

I think it is very normal to go through a period of doubting the celiac diagnosis for a while. There is nothing wrong with that. It is a big change in our lives and takes some adjustment to get used to.

Here is one of the threads on cheating on the gluten-free diet. The only person you cheat is yourself of course. The gluten-free diet gets easier after you have gotten used to it and aren't automatically thinking of the things you used to eat when you get hungry. It's like learning anything new, it is simpler with practice. Over time you don't think of those old gluteny foods as food anymore. And they lose their appeal.

How bad is cheating?

MelissaSH4 Newbie

Hi Melissa...

I am not sure that I can be much help to you...but, I am going to try...

To me, it's not feeling like a freak...it's normal... And, I have a hard time relating to the feeling of "being deprived" and the urge to "cheat" that I read, so often, in here. Please, don't take that to mean that I don't empathize...I totally do! It's just that I don't feel those things. I've actually thought a lot about "why" I don't...

For me, it's simply this:

Gluten is poison...for me and many, many others... Why "feel deprived" about not being able to have "poison"? I equate it to going out to the garage and opening up a jar/can/bottle and taking a big ol' swig...

"Antifreeze" is toxic...deadly, in fact. We, humans know not to drink it...nor do we want to. But, animals think it sweet and tasty! Which is why we humans have to keep dogs/cats/etc away from it (make sure we rinse off that big puddle from the driveway, etc). I, also, know that grapes and chocolate (to name a couple) are toxic to my dogs so, I make sure they don't get access to the stuff... I don't feel sad for them, though. I know it's for the best...

"Cheating"? Same thing...it's POISON. I don't, honestly, care that others get to have "it". In fact, I feel sorry for them (I don't think gluten is "good" for anybody...just my perspective).

Perhaps if you can, really, come to the understanding of just how "deadly" (and, yes, gluten is "deadly" to the celiac/gluten intolerant) it is to you, it won't be such an emotional struggle?

I know this might sound simplistic...it's just how I feel...

Last, but very important, if you continue to feel this way, don't hesitate to get some help... Maybe a therapist could help you sort through it all?

I hope you can find peace so you can move forward...happily and in good health.

:)

Thank you so much for taking the time to share your perspective. I sincerely appreciate it. To be totaly homest with you I have NEVER thought of it that way and in reading your response I had a total "Duh Idiot why did't you ever think of that" moment. Instead of focusing on how much better I feel I was totally stuck on how deprived I felt. So thank you for leading me to that moment of clarity.

MelissaSH4 Newbie

Hi,

It sounds like you had pretty severe symptoms before you were diagnosed and went on the gluten-free diet. Any negative reaction to eating gluten is a sign that you shouldn't be eating it. Your body isn't playing games or trying to fool you if it starts reacting. You may not have severe reactions right away but most likely you would develop them over time if you went back on the gluten eating way. Damage can build up and get worse and worse. And spread to other parts of the body besides the gut. People die from celiac disease. Some people have no symptoms at all and they are termed "silent celiacs". Probably most of them are not diagnosed and walk around eating gluten thinking everything is fine. Which is sad because they will certainly develop problems over time if they are unable to absorb vitamins or the inflammation causes cancer in their gut, or some other autoimmune disease develops.

You said you improved going gluten-free right? Why do you think that is? Is it because you didn't eat gluten or was your doctor wrong? I don't see how you doctor could have been wrong about celiac if you improved though.

I think it is very normal to go through a period of doubting the celiac diagnosis for a while. There is nothing wrong with that. It is a big change in our lives and takes some adjustment to get used to.

Here is one of the threads on cheating on the gluten-free diet. The only person you cheat is yourself of course. The gluten-free diet gets easier after you have gotten used to it and aren't automatically thinking of the things you used to eat when you get hungry. It's like learning anything new, it is simpler with practice. Over time you don't think of those old gluteny foods as food anymore. And they lose their appeal.

How bad is cheating?

Thank you for taking the time to respond to my post. I sincerely appreciate your advise. I know how bad cheating is and haven't nor do I want to. I think the problem is that I can never put my finger on exactly what contaminated me. My thought was to purposly expose myself to prove that I do in fact have celiac disease once and for all. Western medicine can be vague some times and I think I was banking on the fact that there was a slight chance that it could have been something else.

JNBunnie1 Community Regular

Thank you for taking the time to respond to my post. I sincerely appreciate your advise. I know how bad cheating is and haven't nor do I want to. I think the problem is that I can never put my finger on exactly what contaminated me. My thought was to purposly expose myself to prove that I do in fact have celiac disease once and for all. Western medicine can be vague some times and I think I was banking on the fact that there was a slight chance that it could have been something else.

One time I got glutened by sour cream that had corn starch in it that was contaminated. It took some doing to figure THAT one out!

Ed in Baja Rookie

I totally empathize. My symptoms were "undiagnosed" since they appeared 10 years ago and consequently I lost my career, and progressed to major neurological problems before being diagnosed. But the truth is I feel better and better each day. And have received a great deal of support from the people here in this forum. Anger and despair are certainly temptations, but the gentle and informed opinions of these folks keep me turned toward the positive. Which is essential, in the long run. Much more helpful than the well meaning pity of my family members, who send condolences for this "terrible affliction" that sound like they belong at a funeral LOL!!!

Hang in there, it really does get better. And BTWL, it seems that one has enough accumulated antigens stored in the body to generate flare ups independent of diet for quite a while. gluten-free for a while now and still have some DH lesions on my thighs. OH well.

Ed


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,162
    • Most Online (within 30 mins)
      7,748

    Jean Kemling
    Newest Member
    Jean Kemling
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • DAR girl
      Looking for help sourcing gluten-free products that do not contain potato or corn derived ingredients. I have other autoimmune conditions (Psoriatic Arthritis and Sjogrens) so I’m looking for prepared foods as I have fatigue and cannot devote a lot of time to baking my own treats. 
    • Scott Adams
      I am so sorry you're going through this. It's completely understandable to feel frustrated, stressed, and disregarded after such a long and difficult health journey. It's exhausting to constantly advocate for yourself, especially when you're dealing with so many symptoms and positive diagnoses like SIBO, while still feeling unwell. The fact that you have been diligently following the diet without relief is a clear sign that something else is going on, and your doctors should be investigating other causes or complications, not dismissing your very real suffering. 
    • Oldturdle
      It is just so sad that health care in the United States has come to this.  Health insurance should be available to everyone, not just the healthy or the rich.  My heart goes out to you.  I would not hesitate to have the test and pay for it myself.  My big concern would be how you could keep the results truly private.  I am sure that ultimately, you could not.  A.I. is getting more and more pervasive, and all data is available somewhere.  I don't know if you could give a fake name, or pay for your test with cash.  I certainly would not disclose any positive results on a private insurance application.  As I understand it, for an official diagnosis, an MD needs to review your labs and make the call.  If you end up in the ER, or some other situation, just request a gluten free diet, and say it is because you feel better when you don't eat gluten.      Hang in there, though.  Medicare is not that far away for you, and it will remove a lot of stress from your health care concerns.  You will even be able to "come out of the closet" about being Celiac!
    • plumbago
      Yes, I've posted a few times about two companies: Request a Test and Ulta Labs. Also, pretty much we can all request any test we want (with the possible exception of the N protein Covid test and I'm sure a couple of others) with Lab Corp (or Pixel by Lab Corp) and Quest. I much prefer Lab Corp for their professionalism, ease of service and having it together administratively, at least in DC. And just so you know, Request a Test uses Lab Corp and Quest anyway, while Ulta Labs uses only Quest. Ulta Labs is cheaper than Request a Test, but I am tired of dealing with Quest, so I don't use them so much.
    • Scott Adams
      PS - I think you meant this site, but I don't believe it has been updated in years: http://glutenfreedrugs.com/ so it is best to use: You can search this site for prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
×
×
  • Create New...