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

Blood-related Problems


happiestgirl

Recommended Posts

happiestgirl Newbie

Hi! I've been dx'ed with Celiac for a little over 2 months now, but I think that some kind of something may be coming to a head on my bloodwork. I have been anemic since I was a child, but it is getting progressively and progressively worse. I have family history or both blood and bone cancers. My Hemoglobin and Hematocrit are plummeting, moreso since I have been gluten-free. Is this normal?

Ok, let me back up. My latest numbers are as follows: Hemoglobin:7.4, Hematocrit:27.0, MCV:65, MCH:19.6.

Now. my Platelets are beginning to balloon. On the same set of lab results, my Platelets are 579.

I also had a differential reviewed and confirmed. It stated moderate hypochromasia, and slight microcytosis.

And, of course, both my celiac-glandin things are both positive.

What I am wondering is this: Do you, my fellow celiacs, have the same type results on your Hemo's and Platelets? And should I be tested for other possible anti-immune diseases (like lupus), since I already have one auto-immune disease? I may sound like I am rattling, and maybe I am. It IS late, but I know I'm lucid. I don't want to be the hypochondriac here, but I would sure appreciate any input from anyone with celiac who may (or may not) have simnilar test results and problems.

Thanks for listening and I pray that you are all richly blessed in all your endeavours.

jenn.


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



Celiac.com Sponsor (A8-M):



trents Grand Master

Jen,

Has anyone done a bone marrow biopsy on you lately? The platelets going up are not normal for Celiac disease, though anemia is. Are you on iron supplementation?

Steve

tarnalberry Community Regular

Lymphoma and anemia are both highly correlated to untreated celiac disease. The fact that your gliandin antibodies are still up means that you're not healed yet, so it's not surprising that you're other numbers aren't improving. If your gliandin antibodies didn't decline, you should very carefully analyze your diet, your food preparation area, and your toilettries for hidden gluten to make sure that you are actually gluten free.

aikiducky Apprentice

Two months into the diet though might just not be enough time for the antibodies to go down... especially if you have been making little mistakes and getting some gluten here and there.

Pauliina

trents Grand Master

Just did some research and found out that high platelet counts can be caused by chronic iron deficiency. Didn't know that. That would certainly fit with you.

Open Original Shared Link

Steve

happiestgirl Newbie
I'm not sure this helps any, I'm not a doctor so not even sure this relates to what you are talking about but I'll add just in case.

I have Celiac, I also have Pernicious Anemia, Pernicious anemia is a chronic illness caused by impaired absorption of vitamin B-12 because of a lack of intrinsic factor (IF) in gastric secretions it's also associated with gastric atrophy. I also have a multitude of autoimmune diseases. I have a high sed rate which could mean just inflamation somewhere but they are not ruling out Lupus for me. My red blood cells were large and abnormally shaped.

I don't know what a Hemoglobin and Platelet is LOL but hope this helps in some way.

Thank you so very much for responding (all of you!) My GI doc told me, nay, ordered me, on Thursday to tell my Primary doc to order more tests on me ASAP, including any and all tests for any kind of autoimmune diseases. My RBC's are tiny, pale, and look like frisbees that have been held over a bonfire. My grat-Grandmother died from Bone cancer, so I guess maybe it wouldn't be a bad idea to get my marrow checked, too? I don't know. I'm just scared right now and no one's telling me much. I always ask for test results (copies) so I can make sure I look up stuff that they don't tell me. That way, at least, I can be more informed.

Thank you all again. Maybe I can get to the bottom of this. I hope so, anyway. :) Have a most blessed night/day wherever you are!

Lymphoma and anemia are both highly correlated to untreated celiac disease. The fact that your gliandin antibodies are still up means that you're not healed yet, so it's not surprising that you're other numbers aren't improving. If your gliandin antibodies didn't decline, you should very carefully analyze your diet, your food preparation area, and your toilettries for hidden gluten to make sure that you are actually gluten free.

My GI doctor has tried to explain to me that most of my intestines, in fact, may never heal. I have seen the x-rays and etc. that thay have done, and the damage is amazing. There will be some healing, yes, but she (and the entire rest of her staff of colleagues, all agree that complete healing will never happen. And as a result, my cancer risks have gone from the usual 5-fold, to infinite. But I can live with that. I just want to know what is wrong with my blood. I feel it may be a co-runner with the celiac, but is not caused by it. Any way, it's late and I'm tired, so I am going to get a nap. Sleep sweet, all!

ravenwoodglass Mentor
Thank you so very much for responding (all of you!) My GI doc told me, nay, ordered me, on Thursday to tell my Primary doc to order more tests on me ASAP, including any and all tests for any kind of autoimmune diseases. My RBC's are tiny, pale, and look like frisbees that have been held over a bonfire. My grat-Grandmother died from Bone cancer, so I guess maybe it wouldn't be a bad idea to get my marrow checked, too? I don't know. I'm just scared right now and no one's telling me much. I always ask for test results (copies) so I can make sure I look up stuff that they don't tell me. That way, at least, I can be more informed.

Thank you all again. Maybe I can get to the bottom of this. I hope so, anyway. :) Have a most blessed night/day wherever you are!

My GI doctor has tried to explain to me that most of my intestines, in fact, may never heal. I have seen the x-rays and etc. that thay have done, and the damage is amazing. There will be some healing, yes, but she (and the entire rest of her staff of colleagues, all agree that complete healing will never happen. And as a result, my cancer risks have gone from the usual 5-fold, to infinite. But I can live with that. I just want to know what is wrong with my blood. I feel it may be a co-runner with the celiac, but is not caused by it. Any way, it's late and I'm tired, so I am going to get a nap. Sleep sweet, all!

I think it is a good thing that your doctor is being through and checking all bases. A bone marrow test is not something they would do unless they find a real indication for it's need. They will be able to tell from the blood work if that is something that is indicated. It can take a long time to heal, I am four years into the gluten free life and was close to having my body shut down before it was finally found. The healing process is long, especially for those of us that were over 10 years with serious illness before it is found. The body does have amazing recouperative powers although for many of us late diagnosis folks complete healing is not possible healing to the point where life is worth living again is. Be sure to check everything you come in contact with from household glues to shampoos to hair dye to modeling clays, toiletries, cosmetics, kissing someone who is eating gluten. Even shareing a can opener is risky. It can be a bit overwhelming at first but it will be worth it.


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



Celiac.com Sponsor (A8-M):



penguin Community Regular

Your bloodwork looks a lot like mine. They did an iron study on me because they said those blood levels (low hematocrit, small RBC's, and high platelets) are indicative of one of two things:

1: Iron deficiency anemia

2: Open Original Shared Link

Iron deficiency is caused by long term anemia, which in our cases is likely caused by celiac. With iron deficiency anemia, your platelets balloon and your red blood cells shrink. Hypochromasia means that your red blood cells aren't as red as they should be, and microcytosis means your red blood cells are smaller than they should be. Both are caused by long term anemia.

Thallesemia is a genetic blood disorder mainly affecting those of middle eastern and jewish descent. It's reasonably rare and is related to sickle cell. Usually, your MCV or MCH are ridiculously low. They do an iron study (looking at ferritin, saturation, and iron binding capacity) to see which it is, in my understanding.

Basically, eat more iron rich foods like beans and red meat, and try taking a supplement. Make sure to ask your doctor what strength of iron supplement to take.

loraleena Contributor

I have normal iron, but chronically low platelets - around 130,000. Recently they dipped for a couple months to 84,000, but are back up to 131. They think I have an autoimmune disorder that can destroy platelets, but my levels are fine. They will monitor me 2x year to make sure they don't go below 30,000.

I posted a while back wondering if anyone else had this? It seems like celiac cause a multitude of autoimmune disorders. I'm not sure what yours mean, but it is the opposite of what I have!

lindalee Enthusiast

Altered bile flora can lead to abnormal blood tests and elevated liver enzimes. LL

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,930
    • Most Online (within 30 mins)
      7,748

    Mhp
    Newest Member
    Mhp
    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

    • AnnaNZ
      I forgot to mention my suspicion of the high amount of glyphosate allowed to be used on wheat in USA and NZ and Australia. My weight was 69kg mid-2023, I went down to 60kg in March 2024 and now hover around 63kg (just after winter here in NZ) - wheat-free and very low alcohol consumption.
    • AnnaNZ
      Hi Jess Thanks so much for your response and apologies for the long delay in answering. I think I must have been waiting for something to happen before I replied and unfortunately it fell off the radar... I have had an upper endoscopy and colonoscopy in the meantime (which revealed 'minor' issues only). Yes I do think histamine intolerance is one of the problems. I have been lowering my histamine intake and feeling a lot better. And I do think it is the liver which is giving the pain. I am currently taking zinc (I have had three low zinc tests now), magnesium, B complex, vitamin E and a calcium/Vitamin C mix. I consciously think about getting vitamin D outside. (Maybe I should have my vitamin D re-tested now...) I am still 100% gluten-free. My current thoughts on the cause of the problems is some, if not all, of the following: Genetically low zinc uptake, lack of vitamin D, wine drinking (alcohol/sulphites), covid, immune depletion, gastroparesis, dysbiosis, leaky gut, inability to process certain foods I am so much better than late 2023 so feel very positive 🙂    
    • lehum
      Hi and thank you very much for your detailed response! I am so glad that the protocol worked so well for you and helped you to get your health back on track. I've heard of it helping other people too. One question I have is how did you maintain your weight on this diet? I really rely on nuts and rice to keep me at a steady weight because I tend to lose weight quickly and am having a hard time envisioning how to make it work, especially when not being able to eat things like nuts and avocados. In case you have any input, woud be great to hear it! Friendly greetings.
    • Hmart
      I was not taking any medications previous to this. I was a healthy 49 yo with some mild stomach discomfort. I noticed the onset of tinnitus earlier this year and I had Covid at the end of June. My first ‘flare-up’ with these symptoms was in August and I was eating gluten like normal. I had another flare-up in September and then got an upper endo at the end of September that showed possible celiac. My blood test came a week later. While I didn’t stop eating gluten before I had the blood test, I had cut back on food and gluten both. I had a flare-up with this symptoms after one week of gluten free but wasn’t being crazy careful. Then I had another flare-up this week. I think it might have been caused by Trader Joe’s baked tofu which I didn’t realize had wheat. But I don’t know if these flare-ups are caused by gluten or if there’s something else going on. I am food journaling and tracking all symptoms. I have lost 7 pounds in the last 10 days. 
    • trents
      Welcome to the forum, @Hmart! There are other medical conditions besides celiac disease that can cause villous atrophy as well as some medications and for some people, the dairy protein casein. So, your question is a valid one. Especially in view of the fact that your antibody testing was negative, though there are also some seronegative celiacs. So, do you get reactions every time you consume gluten? If you were to purposely consume a slice of bread would you be certain to develop the symptoms you describe?
×
×
  • 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.