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

Tell Me About Your Repeat Blood Test


1974girl

Recommended Posts

1974girl Enthusiast

Next month, I will take my daughter back for her 6 month check-up. They will see if her levels have fallen since going gluten free. I can't think of any exposure but then again she doesn't show symptoms so I wouldn't know anyway. She has hashimotos thyroid and I know that can raise Ttg, too. On your repeat blood test, did it show normal or does it take years. (I think I have asked this and someone said it took them 3 years) but they tell me I should know if it is working in 6 months. What experiences have you had? Does yours show fine?


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



Celiac.com Sponsor (A8-M):



BabsV Enthusiast

My 6-month blood work showed a marked decline in antibodies -- close to the 'normal/negative' level but still high or above it. The doctor who reviewed the results said that I was obviously responding to the diet but it can take a year or more to get down to the proper levels. He said they don't worry about 'refractory sprue' until it has been at least 2 years post-diagnosis. I'm curious to see what my 1-year blood work will show in a couple months...

upwitht21 Rookie

My 9 year old just had repeat labs after 6 months on the diet and he was in the normal range on everything

1974girl Enthusiast

whew! You give me hope!

StephanieL Enthusiast

We are almost 2 years gluten-free. DS's ttg's dropped but were not back to normal after 18 months. After few strange TSH levels he was dx with a thyroid issue (though they won't say it's hashi's). Because his ttg's were still strange we did a different test (deamineated gliden or something) and we found out that was totally normal which means that his diet was gluten-free but the ttg's were still an issue. We go for the first lab work post thyroid meds in a few weeks and I am curious to see if his ttg's will be normal now that his thyroid is under control.

Good luck!

1974girl Enthusiast

thanks- If they can't find anything with his thyroid, are they checking his liver and for type 1 diabetes too? I know my friend's 4 yr old son does not have celiac but has a liver issue that causes it to be high. My DH has type 1 diabetes and I know that can make it high too. I assumed you have to have symptoms of diabetes but apparently your body makes antibodies for YEARS before you can show symptoms. But if he is showing a thyroid issue, get it worked out immediately. My dd has it and didn't grow for a year. They do the "catch-up" growth though and now she is back to normal. I am scared that my dd Ttg will not be normal. Although the thryoid meds control hormone levels, it does nothing for the antibodies that are continuing to attack her thryoid. We just had the test a few weeks ago and after 4 years, she should be under 35 and she is 2800. I can't imagine that WON'T affect her thryoid. I had heard that going gluten-free would help her thryoid antibodies, too but it didn't. At least not after 5 months. It actually even went up a tad.

StephanieL Enthusiast

Oh no, it is his thyroid. TSH's were all over the place and he's been on synthroid for about 3 months now and and they are normal. They won't dx it as hashi's because his T3 and T4's were not leaning towards that but whatever....I think think it is hashi's but he doesn't fit the clinical picture for them so they won't say it (ya know, like many here know it's Celiac but Dr's don't listen ;) )

Anyway, I am really interested in his blood work to see if the thyroid being under control brings his ttg's to WNL. I think we go in early July.


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



Celiac.com Sponsor (A8-M):



Krussell21 Newbie

Can one be tested to see if they are clear of gluten. I am a 34 year old female, and I was newly diagnosed 10 months ago. It's been a long road, and I am not happy that I have Celiac Disease, but I am happy someone FINALLY found the answer! I am just concerned about the late diagnosis and how damaged my intestines are. I recently had a scope a couple of months ago to check my pancreatic valve, and was told that the damage to my intestines still looks the same. My doctor feels I am still getting gluten somewhere. I am being so very careful, but I realize living with my Husband and our using the same kitchen to cook can cause problems. I have my own section and supplies, but it doesn't mean I am 100% safe, not to mention potential contamination when we eat out. I was just wondering if it was possible to be tested or have a scope on a yearly basis to see if my intestines are repairing or staying the same.....any thoughts? I have been meaning to ask my doctor this question, and will do so at my next appointment.

sa1937 Community Regular

Actually you do not have a late diagnosis. Many people are diagnosed at a much later age. In comparison, I am ancient! laugh.gif

I have an appointment with my GI soon and he has ordered some follow-up celiac tests including the tTG and EMA. Thus far I have not been scoped after I had my initial scope two years ago.

In your case I would be concerned about cross-contamination as I think it would be very difficult living in a mixed household. But I know others can do it successfully.

Silencio Enthusiast

Im scheduled to go for blood tests every 3 months since my diagnosis. I had it done at 3 months and I never heard anything at all from the doctor. My 6 month test is coming up. Should I be expecting a call from the doc? I figured I would hear from them either way so I could find out where im at.

sa1937 Community Regular

Im scheduled to go for blood tests every 3 months since my diagnosis. I had it done at 3 months and I never heard anything at all from the doctor. My 6 month test is coming up. Should I be expecting a call from the doc? I figured I would hear from them either way so I could find out where im at.

Your best bet is personally asking for copies of any lab reports. Call first and then make arrangements to pick them up. I wouldn't necessarily expect the dr. to call. Some just aren't very good at that.

Silencio Enthusiast

Your best bet is personally asking for copies of any lab reports. Call first and then make arrangements to pick them up. I wouldn't necessarily expect the dr. to call. Some just aren't very good at that.

Alright I will do that after I go for my 6 month test. Hopefully im able to get them both. I wont know what the numbers mean but im sure people around here will know all about it.

Cara in Boston Enthusiast

My son (now 7) showed that his levels went down slightly after 6 months, but the doctor felt it should have been more significant. We stepped up our gluten-free efforts (no more "processed in a facility . . ." and no more eating out. His 1 year tests showed everything in normal range.

I guess it just takes time.

cara

  • 2 weeks later...
ncallier Newbie

Can one be tested to see if they are clear of gluten. I am a 34 year old female, and I was newly diagnosed 10 months ago. It's been a long road, and I am not happy that I have Celiac Disease, but I am happy someone FINALLY found the answer! I am just concerned about the late diagnosis and how damaged my intestines are. I recently had a scope a couple of months ago to check my pancreatic valve, and was told that the damage to my intestines still looks the same. My doctor feels I am still getting gluten somewhere. I am being so very careful, but I realize living with my Husband and our using the same kitchen to cook can cause problems. I have my own section and supplies, but it doesn't mean I am 100% safe, not to mention potential contamination when we eat out. I was just wondering if it was possible to be tested or have a scope on a yearly basis to see if my intestines are repairing or staying the same.....any thoughts? I have been meaning to ask my doctor this question, and will do so at my next appointment.

I turned 50 on my last birthday and was diagnosed 4 mos.later. That was nearly 3 mos. ago. I believe that I've had celiac disease most of my life. Because of food sensitivities, I have always watched for what set my digestive symptoms off and have mostly voluntarily and without much thought cut those things from my diet. I, too, believe that I probably have much damage, especially since my symptoms have improved but not as much as I had hoped. I recently had a battery of blood tests performed by endocrinologist, but he didn't do many of the tests I thought he should. He didn't check my vitamin k levels and treated me as though I were an idiot when I asked him about it. I bleed very profusely and have broken capillaries all over my legs, arms, and torso. Although my hemoglobin and hematocrit were normal, my red blood cells were low. Also, my vitamin b-12 and folate were low as was free thyroxine. Can someone please give some advice?

Mom-of-Two Contributor

My GI dr is retesting me only 3 months in, in about two weeks here, with a follow up appt the week following. I have a suspicion my numbers will not be that much lower but I would like to know if I am on the right track, if my numbers are not changed at all I will likely step up my efforts, and eating out. I also have more questions so am happy to be going back.

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
      131,955
    • Most Online (within 30 mins)
      7,748

    Mabelie
    Newest Member
    Mabelie
    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.