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

Celiac & Itp (Low Platlet Bleeding Disorder)


Sheryl589

Recommended Posts

Sheryl589 Newbie

Hello, I'm new to this site and to Celiac disease. However, I'm not new to autoimmune diseases.

My daughter (now 21) was diagnoised in 2002 with idiopathic thrombocytopenic purpura or ITP.

Itp is a disease where the body attaches the blood and destroys the platets. Last week she was

diagnoised with Celiac disease. She has suffered from stomach problems for years. She's been tested

3 times for Lupus. Her list of Celiac symptoms is a tablet sheet long.I've been reading and it seems there is some kind of link diseases. Does anyone else have ITP or have bleeding or bruising problems?


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



Celiac.com Sponsor (A8-M):



knittingmonkey Newbie

Hello, I'm new to this site and to Celiac disease. However, I'm not new to autoimmune diseases.

My daughter (now 21) was diagnoised in 2002 with idiopathic thrombocytopenic purpura or ITP.

Itp is a disease where the body attaches the blood and destroys the platets. Last week she was

diagnoised with Celiac disease. She has suffered from stomach problems for years. She's been tested

3 times for Lupus. Her list of Celiac symptoms is a tablet sheet long.I've been reading and it seems there is some kind of link diseases. Does anyone else have ITP or have bleeding or bruising problems?

Been diagnosed celiac, both my parents might be to; Dad (deceased) had depression and severe mental illness, Mom is diabetic, hypothyroid, congestive heart, scoliosis and seems to have Parkinson's, also suffers with diarrhea.

On Dad's side of the family, his first cousin had known issues with wheat, and his sister had ITP. So yes, I think there may be a connection between celiac and other auto-immune disease.

mommida Enthusiast

There seems to be a saying of "once you have one auto-immune disease it"s just a matter of time before you get another." :ph34r:

A few people here have mentioned small purple bruises, which I believe is a primary symptom of ITP. I have them myself, and have not been able to find a doctor to even now what kind of test to run. :huh:

So as soon as we can find doctors who know enough about auto-immune diseases to even diagnose them, I'm sure we are going to have more of a proven correlation. ;)

Sheryl589 Newbie

Have your doctor order a CBC. It will check your platlet level. ITP is a bleeding disorder. It causes spontaneous bleeding(nose,gums etc.). Bruising is usually severe but not aways. Also you will find peticia. These are small red blister like dots.

I'm wondering now if she's had Celiac most of her life and their just now finding it. If so she might have been able to avoid ITP and years of severe treatment. She also has gasteritis, B12 defic.,reflux disease and the list of symptoms goes on and on.

Looking for answers Contributor

I've had low blood platlets for years....they've never dropped to a dangerously low number but they are usually out of range. I also have gastristis. I believe your daugter will be able to control it from getting any worse by eliminating gluten and possibly dairy.

  • 2 weeks later...
O.N. Rookie

...Does anyone else have ITP or have bleeding or bruising problems?

It was the only symptom that my physician couldn

nikki-uk Enthusiast

My husbands diagnosis of ITP came several years after the celiac disease and psoriatic arthritis was diagnosed.

Luckily the ITP has not yet required treatment - it's just closely monitored.

He's always been an 'easy bleeder'....I think he's had low platelets for alot longer than he's been aware :rolleyes:


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



Celiac.com Sponsor (A8-M):



  • 7 months later...
jensen Newbie

My 5 year old son was diagnosed with a severe case of ITP 2 years ago. He has had tummy aches on and off for years and we were told that it was nothing to be concerned about. He just tested positive with the first blood test for Celiac but his doctor ordered a genetic test that shows that it is not in his DNA. he said he cannot possibly has Celiac if it is not in his genetic makeup. I really feel that his test result is related to his ITP. It is hard to ignore His tummy aches, dry, awful skin and night sweats. Can anyone offer us an explaination? I heard that there are endocrine diseases that can create celiac disease and autoimmune diseases like ITP even if they are not in the patients DNA.

Help.

Searching Mom.

mommida Enthusiast

The genetic tests for Celiac are not failproof.

  • 11 months later...
Austin Guy Contributor

In case anyone is still following this, I had ITP between my ankles and knees for about 5 years. I also bled forever (sometimes for an hour) after nicking myself shaving. I never made the connection until after going gluten free in May, 2011. The ITP was gone in a week and small cuts clotted within a minute or so. In me there was absolutely a strong connection between ITP and gluten. By the way, ITP is now being called Immune Thrombocytopenic purpura. Go figure.

RiceGuy Collaborator

Also you will find peticia. These are small red blister like dots.

Wow, I finally have a name to put on it! Have had this as long as I can remember. Still do, and not until this moment did I connect it to Celiac. Sorta just ignore it most of the time.

And the easy bruising...oh yeah. Blisters too. But these didn't start until long after going gluten-free :huh: Been taking vitamin C, K2, D3, Biotin, Folic acid, and more. Can't find a zinc supplement that doesn't throw my digestive system off. Hopefully I don't really need it.

A work in progress...

  • 4 weeks later...
Tim Lawing Newbie

My son had ITP most of his life. He tested him for Celiac over a year ago and the entire family is living gluten free in south Mississippi. His symptoms has all but disappeared and better yet, we have not had one treatment for his ITP since. His behavior has changed and he is able to pay attention at school. It has taken some time to understand and get used to the diet; however, he is a success story.

Tim Lawing.

  • 3 months later...
nvsmom Community Regular

I had ITP years ago and just searched the forum to see if it was connected to celiac... I guess it might be. Huh. I had a bad case of ITP, I remember my platelets were at 90, not 90K, just 90. lol I almost needed a blood transfusion. Steroids couldn't regulate my blood so they took my spleen out; my white blood cells aren't able to do much any more.

I'm still in the process of diagnosing myself as celiac, although I think I've had it for a good 30 years, but it makes me wonder if celiac caused it or how related they are...

nicole

cavernio Enthusiast

My 5 year old son was diagnosed with a severe case of ITP 2 years ago. He has had tummy aches on and off for years and we were told that it was nothing to be concerned about. He just tested positive with the first blood test for Celiac but his doctor ordered a genetic test that shows that it is not in his DNA. he said he cannot possibly has Celiac if it is not in his genetic makeup. I really feel that his test result is related to his ITP. It is hard to ignore His tummy aches, dry, awful skin and night sweats. Can anyone offer us an explaination? I heard that there are endocrine diseases that can create celiac disease and autoimmune diseases like ITP even if they are not in the patients DNA.

Help.

Searching Mom.

1. You aren't the only person to complain about celiac disease showing up positive in blood tests and symptoms but then have negative genetic results show up.

2. Your doctor is the first I've heard say that there's a 100% agreement with genes and celiac disease. The wikipedia article disagrees with your doctor.

"There are seven HLA-DQ variants (DQ2 and DQ4

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,035
    • Most Online (within 30 mins)
      7,748

    bostonbell
    Newest Member
    bostonbell
    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

    • Jmartes71
      Thankyou so much for your words.Its a hard battle when a supposed well known hospital whose celiac " specialist " has down played me because my colon looks fine and put it in my medical and so pcp doesn't take seriously. In their eyes we all carry that gene.Im having alot of bad days trying to be positive because of it.
    • Scott Adams
      Your experience is both shocking and critically important for the community to hear, underscoring the terrifying reality that cross-contamination can extend into the most unexpected and invasive medical devices. It is absolutely devastating that you had to endure six months of sickness and ultimately sustain permanent vision loss because a doctor dismissed your legitimate, life-altering condition. Your relentless research and advocacy, from discovering the gluten in MMA acrylic to finding a compassionate prosthodontist, is a testament to your strength in a system that often fails celiac patients. While the scientific and medical consensus is that gluten cannot be absorbed through the skin or eyes (as the molecules are too large to pass through these barriers), your story highlights a terrifying gray area: what about a substance *permanently implanted inside the body*, where it could potentially shed microparticles or cause a localized immune reaction? Your powerful warning about acrylic lenses and the drastic difference with the silicone alternative is invaluable information. Thank you for sharing your harrowing journey and the specific, severe neurological symptoms you endure; it is a stark reminder that celiac is a systemic disease, and your advocacy is undoubtedly saving others from similar trauma.
    • Scott Adams
      Those are driving distance from me--I will try to check them out, thanks for sharing!
    • Scott Adams
      I am so sorry you're going through this bad experience--it's difficult when your own lived reality of cause and effect is dismissed by the very professionals meant to help you. You are absolutely right—your violent physical reactions are not "what you think," but undeniable data points, and it's a form of medical gaslighting to be told otherwise, especially when you have a positive HLA-DQ2 gene and a clear clinical picture. Since your current "celiac specialist" is not addressing the core issue or your related conditions like SIBO and chronic fatigue, it may be time for a strategic pivot. Instead of trying to "reprove" your celiac disease to unwilling ears, consider seeking out a new gastroenterologist or functional medicine doctor, and frame the conversation around managing the complications of a confirmed gluten-free diet for celiac disease. Go in and say, "I have celiac disease, am strictly gluten-free, but I am still suffering from these specific complications: SIBO, chronic fatigue, dermatological issues, and high blood pressure linked to pain. I need a partner to help me address these related conditions." This shifts the focus from a debate about your diagnosis to a collaborative plan for your current suffering, which is the help you truly need and deserve to work toward bouncing back.
    • NanCel
      Hello, no I had to have them re done and then used a liner over the top.  Many dentists are not aware of the celiac effects.  Best of luck.   There is other material, yet, very expensive.
×
×
  • 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.