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

Finally Saw Celiac Dr And He Wants Another Blood Test


Laurelf

Recommended Posts

Laurelf Explorer

So, I have been pretty much diagnosed with celiac although the biopsy said "could be early sprue" and the blood came back negative but I have all the symptoms, DH, positive gene test, fecal fat, etc. I had not seen the "official" celiac dr though until yesterday as he cancelled a couple of appointments. So he says to me, "You could have early stage celiac, or a gluten intolerance, or just an inflamed gut - the only way to know is to go back on gluten for ONE MONTH and re-do the blood, and oh yeah, 5 % of celiacs will have a negative blood test anyway. When I went through all my symptoms, he kept saying it could be celiac but might not be. As for my DH, all that's left are scars. He suggested that if it flares during the month of re-glutenizing, to get it biopsied right away before I scratch it (yeah, like I can get an appointment with a dermatologist right away).

So, since I've been dying for Chinese food, I had my husband bring in the food last night. Well, during the night, my behind itched real bad and now today I have really bad gas, bloating and pains. I don't think I can take a month of gluten. Off gluten, I'd been feeling so good - my skin looks wonderful for the first time, no problems with digestion except for occasional cross-contamination problems. The dr said he won't put the "celac diagnosis" on my record until it's "official" because of the health insurance implications ??!!

I asked if my son should be tested and he said if it's "just a gluten intolerance" than no but if it's celiac, then yes.

How important is the official diagnosis? Is it worth a month of pain?

Thanks,

Laurel


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



Celiac.com Sponsor (A8-M):



Wolicki Enthusiast

Quite frankly, I would tell your doctor to go pound sand :angry: Either way, whichever it is, the fix is still a gluten free diet, so what would be the point?

ravenwoodglass Mentor

You have already had a postive biopsy, the gold standard. You become sick when eating gluten, you become well without. What more proof is really needed? A month may not even be enough for a postive blood test and then where will you be and what will you do? If I had to wait for a postive blood for diagnosis I would be dead by now. LOL The choice to follow the doctors directions to gluten yourself to prove to him that you really have an issue with gluten is totally up to you.

jerseyangel Proficient

Laurel, All I can tell you is if it were me I would continue to be strictly gluten-free and never look back. Your biopsy was positive--that should have been enough.

Knowing what I know now from going back on gluten once after going gluten-free for a short while (before I was diagnosed, I went to a Kinesiologist who put me on a cleansing diet that included no gluten--I seriously doubt I was strictly gluten-free since at the time I didn't know what all was involved), you may very well experience symptoms even worse than before as well as find that you are sensitive to other foods in addition to gluten.

I think it's barbaric for a doctor, in light of your biopsy, positive response to the gluten-free diet, and your DH symptoms to "require" you to poison yourself for a month--which, incidentally, is really not enough time to produce a valid result--just to make himself feel better. It's absurd.

Mskedi Newbie

The only benefits I can think of for an official diagnosis are these:

1. Some people might think they can cheat on the diet if they don't have the official diagnosis. You don't sound to be one of them.

2. You can get a tax break on your gluten-free food expenditures (I looked into it -- it didn't look like a big enough break to go through the trouble, but that kind of depends on how you eat).

3. You can say with confidence, "I have Celiac Disease."

Honestly, I never heard of the blood test ever being the deciding factor. With the exception of my sister, everyone in my family who has it has been diagnosed despite negative blood tests. With the biopsy, the DH, the positive gene test, and the symptoms, there's really no question what you have. I'd say, tell the doctor what you went through after your first glutening, tell him you're not going through it, and if he won't write it in your chart you can go to a new doctor or just skip the official diagnosis entirely and keep eating gluten-free.

nora-n Rookie

Here in europe in some coutries one would need an official diagnosis for health insurance, because then they subsidise your gluten-free food.

DH means celiac, do you know that?

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
      131,959
    • Most Online (within 30 mins)
      7,748

    jenny44
    Newest Member
    jenny44
    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.