Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

High Platelet


david's mom

Recommended Posts

david's mom Newbie

My son was diagnosed with celiac in May of this year. He did not have the typical reactions, according to the doctors. The blood test in May came back with a platelet count of 427, they said that's a little high but nothing to worry about. We had another blood test done last week and it came back at 447,which they are saying is still no big deal. When does it become a big deal? He is having problems with things looking like they are far away, that's his way of descibing whatever is happening. It doesn't happen all of the time. And it doesn't seem to affect his vision. We are getting referred to a neurologist. I don't know what to expect or even where to start looking. I knew something was wrong when he was a baby, but was told he would out grow the vomitting. He did have reflux and throat nodules, both of which are healed. Anyway, I just thought I would see if anyone could help educate me on this. Thanks a bunch!


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



Celiac.com Sponsor (A8-M):



julie5914 Contributor

Here's some info I found online. I don't believe that number is something to worry about. It is more something to worry about when it goes above 1,000. It could be a flag that something is going on, but that something is most likely celiac.

Too many platelets is called thrombocytosis. When it is caused by something else, it's secondary, or reactive, which is most likely the case. Here are some causes of secondary high platelet count:

Infection (acute and chronic)

Inflammatory disorders (eg Kawasaki's disease)

Chronic iron deficiency

Acute or chronic blood loss

Tissue damage from trauma or surgery

Medicines (steroid, vincristine)

Splenectomy and hyposplenism

Malignancy (Hodgkin's disease, solid tumours)

Rebound from chemotherapy

In your sons case, with a high count but still not too high, I would guess infection or iron deficiency, as these are likely in celiac.

I'm not a doctor or a nurse or anything though. I just read a lot. :D

david's mom Newbie

Thanks Julie. I found that info too. He's not on any meds for anything and hasn't been sick. I was also told that if he's on a gluten-free diet then he shouldn't have inflammation. I really appreciate you looking stuff up for me. I guess I'll just keep a watch on him and continue to do what we're doing. :)

julie5914 Contributor

I'm gluten free since June and still have all sorts of problems, so it may just take a while. I am like you though, I hate when they don't explain stuff unless it's a big sign something's already wrong. If a number is out of range and possibly going up, I want to stop it before it goes further. If it were that normal, it wouldn't be out of range, would it!

Eliza13 Contributor

I also had a high white blood cell count as part of my symptoms.

  • 6 months later...
helper Newbie

Has anybody out there researched a possible fungus or yeast link to celiac with a high platelet count? I was just reading on an internet site the other day that inflammation may be a cause of platelet count and I know that fungus overgrowth can sure cause inflammation. I also know that there are already some people who write in to celiac.com saying that when they cured their candida yeast problems their celiac symptoms disappeared, also. Yeast is another way of saying fungus, isn't it? Many who suffer Celiac Disease are told that corn is an acceptable grain since there's no gluten so I bet lots of you eat a plenty of it--especially kids. But corn is considered a universally contaminated grain--loaded with molds and fungus, or so I've read. If it were me I would try staying away from foods that not only have gluten but also high fungus or yeast contents like corn, peanuts, mushrooms and stay away from sugar also since yeast/fungus needs sugar to grow. What have you got to lose? I've heard a book that explains some of this reasoning is, The Fungus Link by Doug Kaufmann. He has a show on dish network and cable called, Know the Cause. I believe he has worked with a doctor in Texas who believes the way to treat celiac disease is by supplementing a good gluten-free diet with taking an anti-fungal drug like nystatin or diflucan along with a pro-biotic (good bacteria). This doctor says that a lot of celiac sufferers seem to have been a lot of anti-biotics in the past and may have destroyed the good bacteria that keeps yeast in check. This may not be new information but perhaps it will help someone. There has to be some reason why not everyone is helped by just following a gluten free diet and using the more traditional treatment. Maybe this is the missing link in some of your cases. I heard this discussed on another cable show called, Call to Health. They have a website too. The M.D. and nurse specializing in nutrition on the show seemed to agree with this fungus link idea for some celiac sufferers. I'd check out that book or shows and discuss it with my doctor.

Kaycee Collaborator

Years ago, nearly 20 years ago I had a high platelet count, antibodies, and the doctor thought it was a rumbling appendix. So he did not go further. It was not, but about 5 months later, he realized that I had a cyst besides my ovary about the size of a grapefruit. How he could miss that I don't know.

My question is, would the high levels be related to the cyst, or would it be related to having celiac all those years ago? Could it be both.

Needless to say, I never went back to that doctor, as and for 18 months I had complained about severe abdominal pain, only to be told it was physcosematic, However you spell that), then he thought it was my appendix after the test results came back.

I have only been diagnosed with celiac for 4 months, and would like to know whether I could've had it all those years back. As it is I think have had it for years and years.

Cathy


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,162
    • Most Online (within 30 mins)
      7,748

    Jean Kemling
    Newest Member
    Jean Kemling
    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

    • DAR girl
      Looking for help sourcing gluten-free products that do not contain potato or corn derived ingredients. I have other autoimmune conditions (Psoriatic Arthritis and Sjogrens) so I’m looking for prepared foods as I have fatigue and cannot devote a lot of time to baking my own treats. 
    • Scott Adams
      I am so sorry you're going through this. It's completely understandable to feel frustrated, stressed, and disregarded after such a long and difficult health journey. It's exhausting to constantly advocate for yourself, especially when you're dealing with so many symptoms and positive diagnoses like SIBO, while still feeling unwell. The fact that you have been diligently following the diet without relief is a clear sign that something else is going on, and your doctors should be investigating other causes or complications, not dismissing your very real suffering. 
    • Oldturdle
      It is just so sad that health care in the United States has come to this.  Health insurance should be available to everyone, not just the healthy or the rich.  My heart goes out to you.  I would not hesitate to have the test and pay for it myself.  My big concern would be how you could keep the results truly private.  I am sure that ultimately, you could not.  A.I. is getting more and more pervasive, and all data is available somewhere.  I don't know if you could give a fake name, or pay for your test with cash.  I certainly would not disclose any positive results on a private insurance application.  As I understand it, for an official diagnosis, an MD needs to review your labs and make the call.  If you end up in the ER, or some other situation, just request a gluten free diet, and say it is because you feel better when you don't eat gluten.      Hang in there, though.  Medicare is not that far away for you, and it will remove a lot of stress from your health care concerns.  You will even be able to "come out of the closet" about being Celiac!
    • plumbago
      Yes, I've posted a few times about two companies: Request a Test and Ulta Labs. Also, pretty much we can all request any test we want (with the possible exception of the N protein Covid test and I'm sure a couple of others) with Lab Corp (or Pixel by Lab Corp) and Quest. I much prefer Lab Corp for their professionalism, ease of service and having it together administratively, at least in DC. And just so you know, Request a Test uses Lab Corp and Quest anyway, while Ulta Labs uses only Quest. Ulta Labs is cheaper than Request a Test, but I am tired of dealing with Quest, so I don't use them so much.
    • Scott Adams
      PS - I think you meant this site, but I don't believe it has been updated in years: http://glutenfreedrugs.com/ so it is best to use: You can search this site for prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
×
×
  • Create New...