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

Possible Cd?


Larteun

Recommended Posts

Larteun Newbie

Hello I'm new to the site. I haven't been diagnosed with celiac disease, but after being made aware of the disease by a friend, I find I have many of the symptoms.

After 6 months and many tests my alkaline phosphotase level had reached 1700+ and my family doctor referred me to a gastroenterologist. He determined the alka. phos. was coming from my liver verses my bones. I noticed high alka. phos. levels is one of the symptoms, but it seems the source is usually the bones not the liver. Am I correct? Or can celiac disease cause the liver to increase these levels?

The first thing the gastroenterologist did was put me on 40 mg of prednisone and within a few days I lost the blotted feeling, sever headaches, body aches, and fever. A liver biopicy indicated it could be autoimmune hepatius, but the sample wasn't large enough to be conclusive. After a a few weeks he suggested another biopicy to confirm, and it turned out negative, my liver was in good shape with no damage. The prednisone brought my alka. phos. levels down, and he started to wean me off. The first day completely off my headaches and fever returned. He checked my blood again to find the phos was rising again.

Now I'm on 20 mg a day and it seems to help some, but not as much as originally. I'm taking 600mg ibuprofen 2-3 times a day. I've been through about every test imaginable except my small intestine. I've also seen an infectious disease doctor and an alergist with no results. I see the gastroenterologist again in 2 weeks, and will ask him about celiac disease. He hasn't made any mention of it being a possible cause of my problem, he did say he thought my liver problem was a secondary problem caused by something else.

Sorry this is so long, the main question I have is has anyone know if alka. phos. elevations from the liver can be a result of celiac disease? I want to go to the doctor with as much info as I can get. Thanks for any help, Larry


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



Celiac.com Sponsor (A8-M):



cdford Contributor

Mine is out of range as well and it is definitely my liver as a result of the celiac disease. The simplest way to determine if celiac disease is your problem is to have a celiac panel (blood work) done. It will tell you much.

Larteun Newbie

cdford

Thanks for the response, it may sound strange but this is the best news I've received since seeking medical help for my symptoms. :D

After countless tests without any answers I was finding myself wishing that the next test would find some problem just to give some direction to an end of my misery. I missed so much work the last 2 years, there was a lot of financial stress added to my already miserable list of symptoms.

My spleen is also enlarged and I see that celiac disease is said to effect among other things the spleen, liver, and gall bladder. I have beta thalassemia and I was told this anemia disease is the cause for that.

My gastroenterologist seems to be an excellent doctor. I'm pretty certain he will be more than happy to persue celiac as the problem if I bring it to his attention. From some of the posts I've read it appears many doctors are ignorant about celiac disease.

Thanks again, your confirming the possible relationship between my liver disorder and celiac disease, at least lifted my spirits and I'm looking forward to having this test and hopefully putting these symptoms behind me. :)

Larry

cdford Contributor

Glad to be of help. I hope your gastro doc is as helpful as my first was. It is so much easier when you have support. Make sure you get any testing done prior to going gluten-free to ensure quality test results. Even then, it is possible to get a false negative just not as likely. You may be surprised at how much you will improve after being gluten-free for a while if the root of the problem is really celiac disease.

Larteun Newbie

So far I really like my gastro doc, he seems very concerned about finding the solution to my problems. In the last 4 months he has personally called me at home 11 times. I'm not used to that personal touch from a doctor. :)

That fact that he has made no mention of celiac disease as a possibility seems to be the general lack of knowledge about the disease among most doctors. That's why I want to get as good an understanding of celiac disease before disscussing it with him.

This site has a wealth of info and I'm picking up alot of it here. When the general medical industry as a whole is somewhat ignorant about such things as celiac disease, I feel there's great value in the opinions of the people who are/have gone/going through this condition.

Will be talking to the doc later today. Thanks to all for helping me get some understanding of celiac disease.

Larry

skbird Contributor

Interesting that a high Alk Phosphatase is indicative of celiac disease. I have not been diagnosed with celiac disease but gluten-intolerance, yet my Alk-P has always been lower than the normal range.

My doctor always blows over it, saying no biggie - only worry when it's high. But I did some research and found a reference that says it could indicate pernicious anemia (deficient in B12) so I'm taking that on a regular basis now.

Thanks for the info.

Stephanie

Larteun Newbie

I go in for the blood test tomorrow morning. My gastro doc said he had patients with celiac disease, but didn't think I fit the profile but was happy to explore any possibilities at this point.

I'm not going to wait for the results of the test before starting the gluten-free diet, I'll start it tomorrow after the test.

I was on the atkins diet for 3 months a couple of years ago, probably wasn't completely gluten-free as I wasn't concerned with gluten and eat some processed meats and dressing that may have had gluten added. But I did feel alot better when on it than I had before and since. I figure going gluten-free will be easier than atkins cause I can still have my taters. :) Just have to watch what I put on them, and any seasoning I use on meats.

Thanks for the help, Larry


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.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to MauraBue's topic in Gluten-Free Foods, Products, Shopping & Medications
      1

      Have Tru Joy Sweets Choco Chews been discontinued??

    2. - Scott Adams replied to chrish42's topic in Doctors
      5

      Doctors and Celiac.com

    3. - trents replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      how much gluten do I need to eat before blood tests?

    4. - MauraBue posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      1

      Have Tru Joy Sweets Choco Chews been discontinued??

    5. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      how much gluten do I need to eat before blood tests?

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,259
    • Most Online (within 30 mins)
      7,748

    MauraBue
    Newest Member
    MauraBue
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Scott Adams
      Some of the Cocomels are gluten and dairy-free: https://cocomels.com/collections/shop-page
    • Scott Adams
      Thank you for the kind words! I keep thinking that things in the medical community are improving, but a shocking number of people still post here who have already discovered gluten is their issue, and their doctors ordered a blood test and/or endoscopy for celiac disease, yet never mentioned that the protocol for such screening requires them to be eating gluten daily for weeks beforehand. Many have already gone gluten-free during their pre-screening period, thus their test results end up false negative, leaving them confused and sometimes untreated. It is sad that so few doctors attended your workshops, but it doesn't surprise me. It seems like the protocols for any type of screening should just pop up on their computer screens whenever any type of medical test is ordered, not just for celiac disease--such basic technological solutions could actually educate those in the medical community over time.
    • trents
      The rate of damage to the villous lining of the SB and the corresponding loss of nutrient absorbing efficiency varies tremendously from celiac to celiac. Yes, probably is dose dependent if, by dose dependent you mean the amount of exposure to gluten. But damage rates and level of sensitivity also seem to depend on the genetic profile. Those with both genes HLA-DQ2 and HLA-DQ8 seem to be more sensitive to minor amounts of gluten exposure than those with just one of those genes and those with only DQ2 seem to be more sensitive than those with only DQ8. But there are probably many factors that influence the damage rate to the villi as well as intensity of reaction to exposure. There is still a lot we don't know. One of the gray areas is in regard to those who are "silent" celiacs, i.e. those who seem to be asymptomatic or whose symptoms are so minor that they don't garner attention. When they get a small exposure (such as happens in cross contamination) and have no symptoms does that equate to no inflammation? We don't necessarily know. The "sensitive" celiac knows without a doubt, however, when they get exposure from cross contamination and the helps them know better what food products to avoid.
    • MauraBue
      Help!  My 5 year old daughter just stopped eating dairy and gluten due to her EoE and Celiac.  Her favorite candy in the world is tootsie rolls.  I did some research, and it sounds like these are the only options for finding something similar, but I can't find them anywhere to actually purchase.  Have they been discontinued??  Does anyone have another recommendation for a gluten-free/DF tootsie roll option?
    • catnapt
      I wonder how long it usually takes and if it is dose dependent as well... or if some ppl have a more pronounced reaction to gluten than others   thanks again for all the great info    
×
×
  • 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.