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

If I Knew Then, What I Know Now!


little d

Recommended Posts

little d Enthusiast

Hello all

This is long, so kick back, and hope that ya'll can give me your ideas.

If I knew then, what I know now I would not have gotten teste before starting the diet. Yesterday I went and got my lab results from my GI office, that I no longer go to. It has been almost a year for these labs, 3 dates 6/22/06, 8/21/06 and 9/08/06 I think that I understand these results, even though they say negative.

06/22/06 At this point I had been strickly Gluten free for 3months and the GI told me that it would not make a difference. Everything is in the normal, and seems to be very close to either end.

Celiac panel

Endomysial Antibody IgA Negative

t-Transglutaminase (tTG) IgA 0

Immunoglobulin A, Qn, Serum 284

Metabolic Panel (14)

Glucose 91, BUN 9, Creatinine 0.9, Sodium 140, Potassium 3.9, Chloride 103, Carbon Dioxide 25, Calcium 9.8, Protein Total 7.5, Albumin 4.3, Globulin 3.2, A/G Ratio 1.3, Bili 0.5,

Alkaline Phosphatase 63, AST (SGOT) 14, ALT (SGPT) 12

Sedimentation Rate-Westergren 15

08/21/06 This is my Electrolyte Panel, and CBC before my Endo and colonscope and I had been gluten again at this point. Again everything is normal

E Panel

Sodium 138, Potassium 3.9, Chloride 105, Carbon Dioxide 23

CBC

WBC 5.0, RBC 4.31 Hemoglobin 13.4, Hematocrit 39.1, MCV 90.6, MCH 31.2, MCHC 34.4

RDW 13.3, Platelet count 332, Absolute Neutrophils 2920...Lymphocytes 1580...Monocytes 385...

Eosinophils 95...Basophils 20, Neutrophils 58.4, Lymphocytes 31.6, Monocytes 7.7,

Eosinophils 1.9, Basophils 0.4

09/08/06 At this point when I was told that my scopes where negative I started eating all regular food, gained all weight back that was lost while on diet, and got all my symptoms back in full force.

Antineutrophil Cytoplasmic Ab

Cytoplasmic (C-ANCA) <1:20 Does not give what would be positive

Perunuclear (P-ANCA) <1:20

Atypical pANCA >1:20

Gliadin IgG/IgA Ab Prof, EIA

Antigliadin Abs, IgA 1

> are these the same as from the top or are these totoally differnt?

Antigliadin Abs, IgG 2

Saccharomyces cerevisiae Panel

Saccharomyces cervisiae, IgG

<20.0 negative

Saccharomyces cervisiae, IgG > what does equivocal 20.1 - 24.9 mean ??

<20.0 negative

Thank you to all for all the input of what ya'll think, Now I wish I had done testing before I started eating Gluten Free.

Donna


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



Celiac.com Sponsor (A8-M):



sparkles Contributor

I am confused. If symptoms go away when you are gluten-free, why do you need tests and doctors to tell you that you have a problem with wheat or gluten? Would it be easier to stay on a gluten-free diet if you were given an actual diagnosis of celiac disease or gluten intolerance? In my humble opinion, we are the ones who have control over our bodies. We make decisions every day based on what we think and what we feel. Having a doctor tell me that I have no problem with gluten, when I have the big D, stomach cramps, gas, bloating, etc, when I eat it tells me that I do have a problem with gluten and no test in the world is going to convince me otherwise. I don't mean to be unsympathetic but we have problems based on eating gluten and if not eating gluten makes those problems (or most of them) disappear, it seems like a no brainer to me to just stop eating gluten. I know a young man who is 23 with an abdominal aorta anuerism. He is living with a time bomb inside him and there is nothing that he can do to make that time bomb go away. He has to hope that the docs who are treating him are able to make appropriate decisions. Whereas, celiacs or people who have gluten intolerance, have total control over their treatment.... stop eating gluten! There is nothing invasive about the "cure". I know that I have permanent problems caused from gluten.... neuropathy, for one.... and I had colon cancer linked I am sure to the celiac disease but I do have control over my diet. No test in the world would convince me that I can eat gluten again. I know how I feel. The docs don't and the tests certainly do not.

You might consider ignoring the tests and doing what your body tells you is right. A gluten free diet is not going to hurt you. It is a healthy diet.

mn farm gal Apprentice

I am another one that would never go by test results myself. I have doctored for years before even hearing about the disease and my test said neg, but I was gluten light for a year. Not for Celiac but because I was trying to loose some weight so I wasn't eating pasta, bread and baked goods. I know nothing about the test but I am sure someone will.

little d Enthusiast

sparkles

Yes you are right it would be easier for me with a diagnosis from a doctor to stay Gluten free and I do feel better when i am eating better for myself, but I am slowly coming to the reality that I not going to get what I am after. My husband is the type of person who will listen to what doctors say and will do what they say, but he is also that way about work issues as well, follow the rules and yes some of that mentallity has rubbed off on me. My mom did not take me to doctors when I was little and I only remember getting shots going to the community health clinic, We did not have a lot of money back then. So if I did go the doctor it was when I was sick with broncitis or the pnomonia. It was only until I got older that I would go to the doctor myself when I had a job in my early 20's that had insurance, that is when I got diagnosed with Karotosis polaris I know that is spelled wrong. I was very small (I'm still small)in stature when I was little maybe to the point of failure to thrive, I don't know but my mom who I love very much was very backwoods back then. She was dirt poor when she was growing up and didn't think that it was too important. But now she takes good care of her health because of us kids who hound her about her health. I can admite that I am learning about celiac disease and understanding more and trying to understand that getting a diagnoses is not important it is my body telling me what it needs not a doctor telling me. If I wasn't for me braking my foot March 20 when my GI called to see if I wanted to go to another GI I may have said yes, but I have to concentrate on getting my foot better so I'm not going to worry about that anymore, If I need any blood work done I'll just go to my Family doctor to check my levels every once in a while, which it has been a year since I last had any blood test done.

Donna

tiredofdoctors Enthusiast

Donna -- what were the values that were considered Within Normal Limits for the Westergren Sedimentation Rate? The fifteen caught my eye.

I'm a "neurological celiac". The only damage which has been done is to my cerebellum. All my antibodies were normal with the exception of the antigliadin antibodies, which were high. Those are what were damaging my cerebellum. My biopsy was negative, as well.

What is interesting, though, is that since I have been gluten-free, my "irritable bowel syndrome", or "ulcerative colitis", and all the other things that I was diagnosed with are gone. I haven't had one bout of diarrhea since being gluten-free, almost two years now.

I think if you FEEL better being gluten-free, to heck with the lab values. If your symptoms are decreasing, your energy is increasing and life is better, STAY gluten-free. It can't hurt, and if you're a neurological celiac, it will CERTAINLY prevent some pretty terrible stuff.

little d Enthusiast

tiredofdoctors

WOW! I had no idea that the Sedimentation could be a problem nuerologically, I belieave the normal range was 0 - 20 or 25 I can't remember I don't have the results in front of me because I'm at work. What are the neurological problems or symptoms of what you are talking about, I asked someone and now I can't find the post anywhere. But I felt that the Sedimentation rate was a little high myself. Had no idea that could be a factor in anything, I don't know much about chemistry, briefly touched it in Medical assisting school, did one on myself but had to leave for the day before I could see the results.

Thanks for responding

Donna

jacob'smom Newbie
tiredofdoctors

WOW! I had no idea that the Sedimentation could be a problem nuerologically, I belieave the normal range was 0 - 20 or 25 I can't remember I don't have the results in front of me because I'm at work. What are the neurological problems or symptoms of what you are talking about, I asked someone and now I can't find the post anywhere. But I felt that the Sedimentation rate was a little high myself. Had no idea that could be a factor in anything, I don't know much about chemistry, briefly touched it in Medical assisting school, did one on myself but had to leave for the day before I could see the results.

Thanks for responding

Donna


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



Celiac.com Sponsor (A8-M):



jacob'smom Newbie

Have you ever heard of a genetic test for celiac disease? When my son was having trouble with diagnosis, we had a genetic test which confirmed that he carried the genetic component which could cause celiac disease. His case was then confirmed by the fourth or fifth biposy he had had. I guess we finally found the right doctor. I pursued testing and diagnosis because he is still in school and I needed backing to require the school to modify for the diet and to allow our modifications. I also wanted him to never have questions about why we were doing what we were doing for him and to try to avoid the teenage rebellion that I know is coming...

Hello all

This is long, so kick back, and hope that ya'll can give me your ideas.

If I knew then, what I know now I would not have gotten teste before starting the diet. Yesterday I went and got my lab results from my GI office, that I no longer go to. It has been almost a year for these labs, 3 dates 6/22/06, 8/21/06 and 9/08/06 I think that I understand these results, even though they say negative.

06/22/06 At this point I had been strickly Gluten free for 3months and the GI told me that it would not make a difference. Everything is in the normal, and seems to be very close to either end.

Celiac panel

Endomysial Antibody IgA Negative

t-Transglutaminase (tTG) IgA 0

Immunoglobulin A, Qn, Serum 284

Metabolic Panel (14)

Glucose 91, BUN 9, Creatinine 0.9, Sodium 140, Potassium 3.9, Chloride 103, Carbon Dioxide 25, Calcium 9.8, Protein Total 7.5, Albumin 4.3, Globulin 3.2, A/G Ratio 1.3, Bili 0.5,

Alkaline Phosphatase 63, AST (SGOT) 14, ALT (SGPT) 12

Sedimentation Rate-Westergren 15

08/21/06 This is my Electrolyte Panel, and CBC before my Endo and colonscope and I had been gluten again at this point. Again everything is normal

E Panel

Sodium 138, Potassium 3.9, Chloride 105, Carbon Dioxide 23

CBC

WBC 5.0, RBC 4.31 Hemoglobin 13.4, Hematocrit 39.1, MCV 90.6, MCH 31.2, MCHC 34.4

RDW 13.3, Platelet count 332, Absolute Neutrophils 2920...Lymphocytes 1580...Monocytes 385...

Eosinophils 95...Basophils 20, Neutrophils 58.4, Lymphocytes 31.6, Monocytes 7.7,

Eosinophils 1.9, Basophils 0.4

09/08/06 At this point when I was told that my scopes where negative I started eating all regular food, gained all weight back that was lost while on diet, and got all my symptoms back in full force.

Antineutrophil Cytoplasmic Ab

Cytoplasmic (C-ANCA) <1:20 Does not give what would be positive

Perunuclear (P-ANCA) <1:20

Atypical pANCA >1:20

Gliadin IgG/IgA Ab Prof, EIA

Antigliadin Abs, IgA 1

> are these the same as from the top or are these totoally differnt?

Antigliadin Abs, IgG 2

Saccharomyces cerevisiae Panel

Saccharomyces cervisiae, IgG

<20.0 negative

Saccharomyces cervisiae, IgG > what does equivocal 20.1 - 24.9 mean ??

<20.0 negative

Thank you to all for all the input of what ya'll think, Now I wish I had done testing before I started eating Gluten Free.

Donna

little d Enthusiast

The sedimentation rate values are for 0-20 I looked it up. Is 15 a little too high

Donna

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. - Rogol72 replied to klmgarland's topic in Dermatitis Herpetiformis
      3

      Help I’m cross contaminating myself,

    2. - ShariW commented on Scott Adams's article in Frequently Asked Questions About Celiac Disease
      4

      What are Celiac Disease Symptoms?

    3. - klmgarland replied to klmgarland's topic in Dermatitis Herpetiformis
      3

      Help I’m cross contaminating myself,

    4. - Scott Adams replied to klmgarland's topic in Dermatitis Herpetiformis
      3

      Help I’m cross contaminating myself,

    5. - Scott Adams replied to Jmartes71's topic in Coping with Celiac Disease
      1

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,911
    • Most Online (within 30 mins)
      7,748

    Cici123
    Newest Member
    Cici123
    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

    • Rogol72
      @klmgarland, My dermatitis herpetiformis didn't clear up until I became meticulous about cross contamination. I cut out gluten-free oats and all gluten-free foods, dairy and gluten-free rice. Additionally, getting the right amount of protein for my body weight helped significantly in my body's healing process ... along with supplementing with enough of all the vitamins and minerals ... especially Zinc and Magnesium. I went from 70kg to 82kg in a year. Protein with each meal 3 times daily, especially eggs at breakfast made the difference. I'm not sure whether iodine was a problem for me, but I can tolerate iodine no problem now. I'm off Dapsone and feel great. Not a sign of an itch. So there is hope. I'm not advocating for the use of Dapsone, but it can bring a huge amount of relief despite it's effect on red blood cells. The itch is so distracting and debilitating. I tried many times to get off it, it wasn't until I implemented the changes above and was consistent that I got off it. Dermatitis Herpetiformis is horrible, I wouldn't wish it on anyone.  
    • klmgarland
      Thank you so very much Scott.  Just having someone understand my situation is so very helpful.  If I have one more family member ask me how my little itchy skin thing is going and can't you just take a pill and it will go away and just a little bit of gluten can't hurt you!!!! I think I will scream!!
    • Scott Adams
      It is difficult to do the detective work of tracking down hidden sources of cross-contamination. The scenarios you described—the kiss, the dish towel, the toaster, the grandbaby's fingers—are all classic ways those with dermatitis herpetiformis might get glutened, and it's a brutal learning curve that the medical world rarely prepares you for. It is difficult to have to deal with such hyper-vigilance. The fact that you have made your entire home environment, from makeup to cleaners, gluten-free is a big achievement, but it's clear the external world and shared spaces remain a minefield. Considering Dapsone is a logical and often necessary step for many with DH to break the cycle of itching and allow the skin to heal while you continue your detective work; it is a powerful tool to give you back your quality of life and sleep. You are not failing; you are fighting an incredibly steep battle. For a more specific direction, connecting with a dedicated celiac support group (online or locally) can be invaluable, as members exchange the most current, real-world tips for avoiding cross-contamination that you simply won't find in a pamphlet. You have already done the hardest part by getting a correct diagnosis. Now, the community can help you navigate the rest. If you have DH you will likely also want to avoid iodine, which is common in seafoods and dairy products, as it can exacerbate symptoms in some people. This article may also be helpful as it offers various ways to relieve the itch:  
    • Scott Adams
      It's very frustrating to be dismissed by medical professionals, especially when you are the one living with the reality of your condition every day. Having to be your own advocate and "fight" for a doctor who will listen is an exhausting burden that no one should have to carry. While that 1998 brochure is a crucial piece of your personal history, it's infuriating that the medical system often requires more contemporary, formal documentation to take a condition seriously. It's a common and deeply unfair situation for those who were diagnosed decades ago, before current record-keeping and testing were standard. You are not alone in this struggle.
    • Scott Adams
      Methylprednisolone is sometimes prescribed for significant inflammation of the stomach and intestines, particularly for conditions like Crohn's disease, certain types of severe colitis, or autoimmune-related gastrointestinal inflammation. As a corticosteroid, it works by powerfully and quickly suppressing the immune system's inflammatory response. For many people, it can be very effective at reducing inflammation and providing rapid relief from symptoms like pain, diarrhea, and bleeding, often serving as a short-term "rescue" treatment to bring a severe flare under control. However, experiences can vary, and its effectiveness depends heavily on the specific cause of the inflammation. It's also important to be aware that while it can work well, it comes with potential side effects, especially with longer-term use, so it's typically used for the shortest duration possible under close medical supervision. It's always best to discuss the potential benefits and risks specific to your situation with your gastroenterologist.
×
×
  • 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.