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

Platelets


loraleena

Recommended Posts

loraleena Contributor

I recently had a whole bunch of blood work done. My platelets (which have always been a little low) have dropped from 141,000 to 89,000. I am not having any bleeding problems, but bruise a great deal. I have to get tested again next week, and if still low I have to go to a hemotologist! Has anyone else experienced this either before or after going gluten free? The 141,0000 reading was before going gluten free.

Thanks for your help.


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



Celiac.com Sponsor (A8-M):



amymm Newbie
I recently had a whole bunch of blood work done. My platelets (which have always been a little low) have dropped from 141,000 to 89,000. I am not having any bleeding problems, but bruise a great deal. I have to get tested again next week, and if still low I have to go to a hemotologist! Has anyone else experienced this either before or after going gluten free? The 141,0000 reading was before going gluten free.

Thanks for your help.

Hi there. I have ITP (idiopathic thrombocytopenia purpura). I was diagnosed in 1989 at the age of 20. It is an autoimmune disease in which you have chronically low platelet counts with no explaination (hence-"idiopathic").

I spent lots of years on and off prednisone and eventually had my spleen removed. This helped, except when I had my third child, and my platelets dropped again. They went back up after the delivery.

I only found out about celiac/gluten intolerance after the birth of my 2nd child. I really think this is the cause of my ITP. I have read of some possible connection between ITP and celiac.

Don't freak out too much. A count of 89K isn't too bad yet. A hematologist is a great next step. Let me know if you have any other questions.

Amy

loraleena Contributor

Hi, thanks for your reply. I read about that and thats what I suspect, since my other readings are normal. I absolutely will not take steroids. I have already started looking into natural alternatives and have found some chinese herbs that are used for this. Obviously I will not pursue anything until I know for sure. Did going gluten free help your levels? Mine are lower since gluten free. How low did yours go? When do they feel you have to address it ( how low can levels get without intervention). This is so lame, I am a walking autoimmune disease!! Thanks for the help.

amymm Newbie
Hi, thanks for your reply. I read about that and thats what I suspect, since my other readings are normal. I absolutely will not take steroids. I have already started looking into natural alternatives and have found some chinese herbs that are used for this. Obviously I will not pursue anything until I know for sure. Did going gluten free help your levels? Mine are lower since gluten free. How low did yours go? When do they feel you have to address it ( how low can levels get without intervention). This is so lame, I am a walking autoimmune disease!! Thanks for the help.

Hi again. I'm glad you replied. I had my spleen removed in 1999 and this has pretty much taken care of my platelet counts, so I can't say if going gluten free would have helped the platelets. I have read of such an experience.

I wanted to caution you about the chinese herbs. I'm actually very open to alternative treatments myself, especially since I've had many bad experiences with allopathic doctors. But if you platelets dropped below 50K, I would take it very seriously. The same day I read your response, I read about a young woman who refused steroids and decided to take chinese herbs. She ended up bleeding to death because she had 0! platelets in her system, but wasn't aware of it.

I hate steroids myself, spent many years on and off of them and I agree they should be the last option. But they saved my life and my unborn childrens' lives-so they are the worst "miracle drug" out there. Can you get a standing order from your hemotologist to get a platelet count whenever you are worried your count is low? I had that for years and it gave me comfort to know I could have them checked at any time without calling the doctor. Believe me, if they are dangerously low, you'll get a call quick. I once got a call from my OB/GYN on a Saturday morning around 8am-he was freaked because my count was 24K and I was pregnant.

ITP is very unpredictable-please take it seriously if that's what it is. I am happy to talk to you anytime via email.

Good luck and let me know how it goes.

Amy, San Jose

  • 6 months later...
nikki-uk Enthusiast

My husband went to see a haemotologist today as he has consistently had low platelets for the last few months.

He was originally referred by his Rheumatologist as the low platelet count co-incided with him taking a new drug for his Psoriatic Arthritis.

Unfortunately - although the drug worked wonders with his joints he was adviced to stop taking it in case it was this that caused the low platelet count.

However today - the haemotologist said after doing some research that he didn't think this was drug induced and that hubby may have another auto-immune disease called ITP :rolleyes:

He now wants him to have a scan of his stomach to check his spleen and liver (?)

The weird thing is hubby doesn't seem to have any bruises ,- although his gums bleed when he brushes them and if he cuts himself shaving he seems to bleed for ages.

Does anyone else have this?-

Can your platelet count flutuate and return to normal without steroids?

Is ITP common in coeliacs??

Thanks (concerned wife!! :unsure: )

oceangirl Collaborator
My husband went to see a haemotologist today as he has consistently had low platelets for the last few months.

He was originally referred by his Rheumatologist as the low platelet count co-incided with him taking a new drug for his Psoriatic Arthritis.

Unfortunately - although the drug worked wonders with his joints he was adviced to stop taking it in case it was this that caused the low platelet count.

However today - the haemotologist said after doing some research that he didn't think this was drug induced and that hubby may have another auto-immune disease called ITP :rolleyes:

He now wants him to have a scan of his stomach to check his spleen and liver (?)

The weird thing is hubby doesn't seem to have any bruises ,- although his gums bleed when he brushes them and if he cuts himself shaving he seems to bleed for ages.

Does anyone else have this?-

Can your platelet count flutuate and return to normal without steroids?

Is ITP common in coeliacs??

I had idiopathic thrombocytopenia during both my pregnancies. Also, low white count. My doctor is curious to see if being gluten-free for a bit more will bring those numbers up. They are not excessively low right now but have always been on the low side. We'll see. Just had some bloodwork done- I'll post if they've come up.

lisa

Thanks (concerned wife!! :unsure: )

Okay, I just screwed up that response somehow- maybe it can be figured out. Sorry!

lisa

loraleena Contributor

Hi

I am the one who originally started this post back in April. Yes, platelets can go up and down. A month after my platelets dropped to 84, 000, but 2 wks later they were back up to 134,000. The last number has been my normal for years. I do bruise easy, but that is it. Apparently any infection and several types of meds can cause this. The doc does think I have ITP, but now just wants to test me every 6 months, unless I start having issues. He told me that they do not intervene unless you get to 30,000. At the time of the original low count, I had a active cold sore and suspect that may have affected the count as well. I did have a scan of my spleen and liver and they were ok.


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



Celiac.com Sponsor (A8-M):



nikki-uk Enthusiast
Hi

I am the one who originally started this post back in April. Yes, platelets can go up and down. A month after my platelets dropped to 84, 000, but 2 wks later they were back up to 134,000. The last number has been my normal for years. I do bruise easy, but that is it. Apparently any infection and several types of meds can cause this. The doc does think I have ITP, but now just wants to test me every 6 months, unless I start having issues. He told me that they do not intervene unless you get to 30,000. At the time of the original low count, I had a active cold sore and suspect that may have affected the count as well. I did have a scan of my spleen and liver and they were ok.

Thanks Loraleena.

I'm not sure what my hubby's platelet numbers were but the doc said (other than the scan) he will just see him again in January to keep an eye on his levels.I don't think they can be that bad as he doesn't even seem to have any bruises!

I just dreaded another auto-immune diagnosis! :)

TiffTiff Rookie

ive had itp for 7 years i know all about it if you have any ?s feel free to ask, its not as bad as it seems, ive had a child....

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
      131,957
    • Most Online (within 30 mins)
      7,748

    Dogdad21
    Newest Member
    Dogdad21
    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.