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

New Celiac With Questions


KristaleeJane

Recommended Posts

KristaleeJane Contributor

So after thinking that I would never find out why I felt like a peice of #*@! for so long

Symptoms including:

Migranines, Fatigue, stomach issues, low blood sugar, puffiness, muscle cramps and spasms, possible arthritus, never diagnosed though, acne, ichyness etc.

I had an upper GI done, came back normal, had some sort of breath test done where they look for a bacteria for ulcers, came back normal. My doctor said she would like to do some blood work on me, I didn't even know what she was testing me for. She called me 2 days later to come back as she would need to do further testing. My results were very high, normal for the antibody is 20, mine was 92, so she gave me a referal to a specialist for the biopsy, now I am just waiting.

Dying to start the gluten free diet, but waiting patiently, first you have to do consultation, and then you get your appointment for the biopsy, could be a while. In the mean time life is on hold I guess, we had plans to have a baby, but looks like that may not be possible for a while.

Does anyone know what other tests I should ask my doctor to do since my levels were so High of the anitbody. What blood work should I have done, to check my vitamin levels, and is there any other tests that I should have done for osteoperosis, since I have been have a lot of muscle pains and spasms.

Any help would be appreciated

thanks


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

If you have had positive blood work then you have a reaction to gluten. It is your choice whether you want to biopsy or not. The biopsies have also been know to be falsely negative. You have 22 ft of small intestine and if damage is patchy or in an area that the scope can not get to then you will have a false negative. You can also be told the test is negative when preceliac changes are present but not recognized or not yet 'full blown, villi totally destroyed, celiac.'

You should ask your doctor to do a full blood work up on all vitamin and mineral blood levels, do a CBC,a complete blood count to check for anemia and make sure they check folate and B12 levels, they can call sometimes call in the tests to avoid waiting for an appointment. Worth asking. You also should have a bone density scan, another thing that they may just call or send in an order for with your recent bloodwork.

Do be sure to try the diet, strictly even if those biopsies are negative. The blood work is really pretty diagnostic in itself when it is positive. I am sure others will be on with any tests I may have forgotten, I hope you get some relief soon.

KristaleeJane Contributor
If you have had positive blood work then you have a reaction to gluten. It is your choice whether you want to biopsy or not. The biopsies have also been know to be falsely negative. You have 22 ft of small intestine and if damage is patchy or in an area that the scope can not get to then you will have a false negative. You can also be told the test is negative when preceliac changes are present but not recognized or not yet 'full blown, villi totally destroyed, celiac.'

You should ask your doctor to do a full blood work up on all vitamin and mineral blood levels, do a CBC,a complete blood count to check for anemia and make sure they check folate and B12 levels, they can call sometimes call in the tests to avoid waiting for an appointment. Worth asking. You also should have a bone density scan, another thing that they may just call or send in an order for with your recent bloodwork.

Do be sure to try the diet, strictly even if those biopsies are negative. The blood work is really pretty diagnostic in itself when it is positive. I am sure others will be on with any tests I may have forgotten, I hope you get some relief soon.

Thank-you so much for your responcse, I will make sure to follow up with the blood work and bone densily scan. I will definalty do a strict gluten free diet starting after the biopsy regardless of the results, considering how high my blood test came back.

Thanks again for your advise, really appreciate it

Wonka Apprentice
Thank-you so much for your responcse, I will make sure to follow up with the blood work and bone densily scan. I will definalty do a strict gluten free diet starting after the biopsy regardless of the results, considering how high my blood test came back.

Thanks again for your advise, really appreciate it

Once I finally had the appointment with the GI specialist (took 3 months) I was in having a biopsy within a week.

MDRB Explorer
So after thinking that I would never find out why I felt like a peice of #*@! for so long

Symptoms including:

Migranines, Fatigue, stomach issues, low blood sugar, puffiness, muscle cramps and spasms, possible arthritus, never diagnosed though, acne, ichyness etc.

I had an upper GI done, came back normal, had some sort of breath test done where they look for a bacteria for ulcers, came back normal. My doctor said she would like to do some blood work on me, I didn't even know what she was testing me for. She called me 2 days later to come back as she would need to do further testing. My results were very high, normal for the antibody is 20, mine was 92, so she gave me a referal to a specialist for the biopsy, now I am just waiting.

Dying to start the gluten free diet, but waiting patiently, first you have to do consultation, and then you get your appointment for the biopsy, could be a while. In the mean time life is on hold I guess, we had plans to have a baby, but looks like that may not be possible for a while.

Does anyone know what other tests I should ask my doctor to do since my levels were so High of the anitbody. What blood work should I have done, to check my vitamin levels, and is there any other tests that I should have done for osteoperosis, since I have been have a lot of muscle pains and spasms.

Any help would be appreciated

thanks

If you have made up your mind to get the biopsy: whatever you do, do NOT go gluten free prior to having the endoscopy! I went gluten free for six months before deciding to get tested. After seeing the gastroenterologist I was told that I needed to go back on the gluten for 4 weeks before the biopsy for it to be accurate. They were the WORST 4 weeks of my life! My body was just starting to heal and reacted quite severly to the gluten being re introduced.

Good luck :)

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. - knitty kitty replied to pothosqueen's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      16

      Positive biopsy

    2. - knitty kitty replied to Jordan Carlson's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Fruits & Veggies

    3. - knitty kitty replied to pothosqueen's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      16

      Positive biopsy

    4. - trents replied to pothosqueen's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      16

      Positive biopsy

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

    • Total Members
      133,018
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • knitty kitty
      In the study linked above, the little girl switched to a gluten free diet and gained enough weight that that fat pad was replenished and surgery was not needed.   Here's the full article link... Superior Mesenteric Artery Syndrome in a 6-Year-Old Girl with Final Diagnosis of Celiac Disease https://pmc.ncbi.nlm.nih.gov/articles/PMC6476019/
    • knitty kitty
      Hello, @Jordan Carlson, So glad you're feeling better.   Tecta is a proton pump inhibitor.  PPI's also interfere with the production of the intrinsic factor needed to absorb Vitamin B12.  Increasing the amount of B12 you supplement has helped overcome the lack of intrinsic factor needed to absorb B12. Proton pump inhibitors also reduce the production of digestive juices (stomach acids).  This results in foods not being digested thoroughly.  If foods are not digested sufficiently, the vitamins and other nutrients aren't released from the food, and the body cannot absorb them.  This sets up a vicious cycle. Acid reflux and Gerd are actually symptoms of producing too little stomach acid.  Insufficient stomach acid production is seen with Thiamine and Niacin deficiencies.  PPI's like Tecta also block the transporters that pull Thiamine into cells, preventing absorption of thiamine.  Other symptoms of Thiamine deficiency are difficulty swallowing, gagging, problems with food texture, dysphagia. Other symptoms of Thiamine deficiency are symptoms of ADHD and anxiety.  Vyvanse also blocks thiamine transporters contributing further to Thiamine deficiency.  Pristiq has been shown to work better if thiamine is supplemented at the same time because thiamine is needed to make serotonin.  Doctors don't recognize anxiety and depression and adult onset ADHD as early symptoms of Thiamine deficiency. Stomach acid is needed to digest Vitamin C (ascorbic acid) in fruits and vegetables.  Ascorbic acid left undigested can cause intestinal upsets, anxiety, and heart palpitations.   Yes, a child can be born with nutritional deficiencies if the parents were deficient.  Parents who are thiamine deficient have offspring with fewer thiamine transporters on cell surfaces, making thiamine deficiency easier to develop in the children.  A person can struggle along for years with subclinical vitamin deficiencies.  Been here, done this.  Please consider supplementing with Thiamine in the form TTFD (tetrahydrofurfuryl disulfide) which helps immensely with dysphagia and neurological symptoms like anxiety, depression, and ADHD symptoms.  Benfotiamine helps with improving intestinal health.  A B Complex and NeuroMag (a magnesium supplement), and Vitamin D are needed also.
    • knitty kitty
      @pothosqueen, Welcome to the tribe! You'll want to get checked for nutritional deficiencies and start on supplementation of B vitamins, especially Thiamine Vitamin B 1.   There's some scientific evidence that the fat pad that buffers the aorta which disappears in SMA is caused by deficiency in Thiamine.   In Thiamine deficiency, the body burns its stored fat as a source of fuel.  That fat pad between the aorta and digestive system gets used as fuel, too. Ask for an Erythrocyte Transketolace Activity test to look for thiamine deficiency.  Correction of thiamine deficiency can help restore that fat pad.   Best wishes for your recovery!   Interesting Reading: Superior Mesenteric Artery Syndrome in a 6-Year-Old Girl with Final Diagnosis of Celiac Disease https://pubmed.ncbi.nlm.nih.gov/31089433/#:~:text=Affiliations,tissue and results in SMAS.  
    • trents
      Wow! You're pretty young to have a diagnosis of SMA syndrome. But youth also has its advantages when it comes to healing, without a doubt. You might be surprised to find out how your health improves and how much better you feel once you eliminate gluten from your diet. Celiac disease is an autoimmune disorder that, when gluten is consumed, triggers an attack on the villous lining of the small bowel. This is the section of the intestines where all our nutrition is absorbed. It is made up of billions of tiny finger-like projections that create a tremendous surface area for absorbing nutrients. For the person with celiac disease, unchecked gluten consumption generates inflammation that wears down these fingers and, over time, greatly reduces the nutrient absorbing efficiency of the small bowel lining. This can generate a whole host of other nutrient deficiency related medical problems. We also now know that the autoimmune reaction to gluten is not necessarily limited to the lining of the small bowel such that celiac disease can damage other body systems and organs such as the liver and the joints and cause neurological problems.  It can take around two years for the villous lining to completely heal but most people start feeling better well before then. It's also important to realize that celiac disease can cause intolerance to some other foods whose protein structures are similar to gluten. Chief among them are dairy and oats but also eggs, corn and soy. Just keep that in mind.
    • pothosqueen
×
×
  • 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.