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

What I Don't Understand


cathybee

Recommended Posts

cathybee Newbie

I was told I had Celiac in 2005 by a blood test. I went on the diet, found this board ...just read mostly cause I don't have all the trouble most of you do so I just don't feel like part of the group. If I eat wheat by accident I don't even know it cause I don't have any side affects. The only reason they even tested me was I have arthritis bad and they could not find out why it was staying so inflamed and ran a lot of test on me.

With me, dairy hurts me more then gluten and all it does is gives me bad stomach pains.

I would have to say my mom had Celiac Disease from what I read but they never diagnosed it as that and only said she had allergies to wheat. She died never knowing what she had. I took care of her and know what she went through...a lot of what I read here in the board.

So here I am thinking I must have it since mama did and the blood test said so...right? Don't get me wrong, I don't want more then I have right now but wonder if I was missed diagnosed. My arthritis is still bad and inflamed and they can't find anything to help me with the pain so I am now crippled with it. Is there anyone else like me here?


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



Celiac.com Sponsor (A8-M):



RiceGuy Collaborator

As I understand it, Celiac can sorta sneak up on you. So you might not have noticeable symptoms now, but continuing to eat gluten could lead to it going full-throttle. The problem with dairy is common as I'm sure you know. What matters is not just how you feel, but how your body does on the inside. If gluten causes the autoimmune response in you as it does in any Celiac, then you need to remain gluten-free. Not doing so will eventually lead to enough intestinal damage such that you will be forced to take notice, and by that time you'd have big problems.

I guess my question is what about getting a biopsy/colonoscopy/etc to check for damage? Also, how long have you been on the gluten-free diet, and have you also checked your skin/hair care products, dish soaps, etc?

I never bothered with getting tested, so I'm not quite sure what tests would be most appropriate for you at this time. I do know however that it can take a long time for certain conditions to show signs of healing. I'm probably nearing 3 years gluten-free and still it's a mighty struggle on a daily basis.

ravenwoodglass Mentor

Hi and welcome to the boards. I did not have any tummy problems that I thought signified anything for many years. Mostly D associated closely with my periods and constant tummy rumbles. It wasn't until after my DD was born that the daily D set in. But I had joint, skin,balance and muscle problems since childhood.

One of the most painful was the arthritis. By the time I was diagnosed considerable damage had been done to my joints, in particular my hands. They hurt so bad that I had trouble even holding a cup, opening jars was close to impossible and painting or holding my glass tools was out of the question. When I was finally diagnosed the last thing I expected was to have my arthritis go away. I, in a way, was lucky because the damage to my intestines was so severe that I react to even the smallest amount of CC. I found that before the arthritis went into remission that I had to eliminate the gluten from everything I came in contact with or ate. This included shampoos and art and home repair supplies and even my pet food.

One thing that you need to do today is get ahold of your pharmacist and gather together all your OTC drugs and call the makers. There are no regulations by the FDA about gluten in meds or about the need to let us know it is in there. Your biggest risk are things like Tums and generic brands of script drugs. With no resolution to your arthritis after all this time I would be willing to bet you are getting gluten somewhere. You need to have those blood tests run about every six months or so to check and see if your levels have gone down.

Your not alone, there are some folks here or folks that have a family member who is celiac and 'asymptomatic', or who think they are. My DH didn't think he had symptoms after a positive blood test but after a couple months totally gluten-free he came to realize that many things he thought were just a normal part of ageing or being a guy really were not.

I hope you get some relief soon, all I have left now after 5 years gluten-free is knobby joints but no pain. It took about 6 months strictly gluten-free to get to that point but now my arthritis doesn't even flare with a good glutening.

mftnchn Explorer

Hi, just wonder if they also checked you for Lyme disease? Sound like you didn't have a biopsy?

Also have you been really strict on the gluten free or just avoiding obvious wheat products?

I am glad you are asking, and hopefully you'll get a number of responses that will help you.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,029
    • Most Online (within 30 mins)
      7,748

    Nancy N Rosen
    Newest Member
    Nancy N Rosen
    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
      Your experience is both shocking and critically important for the community to hear, underscoring the terrifying reality that cross-contamination can extend into the most unexpected and invasive medical devices. It is absolutely devastating that you had to endure six months of sickness and ultimately sustain permanent vision loss because a doctor dismissed your legitimate, life-altering condition. Your relentless research and advocacy, from discovering the gluten in MMA acrylic to finding a compassionate prosthodontist, is a testament to your strength in a system that often fails celiac patients. While the scientific and medical consensus is that gluten cannot be absorbed through the skin or eyes (as the molecules are too large to pass through these barriers), your story highlights a terrifying gray area: what about a substance *permanently implanted inside the body*, where it could potentially shed microparticles or cause a localized immune reaction? Your powerful warning about acrylic lenses and the drastic difference with the silicone alternative is invaluable information. Thank you for sharing your harrowing journey and the specific, severe neurological symptoms you endure; it is a stark reminder that celiac is a systemic disease, and your advocacy is undoubtedly saving others from similar trauma.
    • Scott Adams
      Those are driving distance from me--I will try to check them out, thanks for sharing!
    • Scott Adams
      I am so sorry you're going through this bad experience--it's difficult when your own lived reality of cause and effect is dismissed by the very professionals meant to help you. You are absolutely right—your violent physical reactions are not "what you think," but undeniable data points, and it's a form of medical gaslighting to be told otherwise, especially when you have a positive HLA-DQ2 gene and a clear clinical picture. Since your current "celiac specialist" is not addressing the core issue or your related conditions like SIBO and chronic fatigue, it may be time for a strategic pivot. Instead of trying to "reprove" your celiac disease to unwilling ears, consider seeking out a new gastroenterologist or functional medicine doctor, and frame the conversation around managing the complications of a confirmed gluten-free diet for celiac disease. Go in and say, "I have celiac disease, am strictly gluten-free, but I am still suffering from these specific complications: SIBO, chronic fatigue, dermatological issues, and high blood pressure linked to pain. I need a partner to help me address these related conditions." This shifts the focus from a debate about your diagnosis to a collaborative plan for your current suffering, which is the help you truly need and deserve to work toward bouncing back.
    • NanCel
      Hello, no I had to have them re done and then used a liner over the top.  Many dentists are not aware of the celiac effects.  Best of luck.   There is other material, yet, very expensive.
    • sleuth
      He is not just a psychiatrist.  He is also a neuroscientist.  And yes, I have already read those studies.   I agree with benfotiamine.  This is short term while glutened/inflammation occurs.  As I had already mentioned, these symptoms no longer exist when this phase passes.  And yes, I know that celiac is a disease of malnutrition.  We are working with a naturopath.
×
×
  • 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.