Jump to content
  • 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):

Is This Celiac Disease?


tiredgradstudent

Recommended Posts

tiredgradstudent Newbie

I am a grad student, a wife, and a mom. Needless to say, I am busy. But for the last 5 years (when I was 19 - I am now 24), I have had gastrointestinal problems that no one can pinpoint.

For as long as I can remember, I have had constipation.

I started having bouts of nausea, bloating, and abdominal pain so severe that just the thought of food would make me want to vomit. I was initially diagnosed with gastroenteritis.

The symptoms didn't go away. They progressively began to last longer. The nausea was no longer as severe but it was constant. This time, I was given an endoscopy and colonoscopy. Nothing was found. I was diagnosed with acid reflux and told to avoid spicy things and caffeine.

The change in diet didn't help. Another trip to the doctor and I was given the diagnosis of lactose intolerance.

The symptoms were relatively constant and the multiple diagnoses just frustrated me. I gave up on the doctor and just decide to live with it (with a lot of tums, peto, and pain killers). I got married and had a son. The symptoms were about the same through the pregnancy.

When my son was 4 months old, I started having horrible migraines. Before the headache, I would not be able to see because a gray fog would descend on my visual fields. The doctor diagnosed them and gave me a description. It didn't seem to help the headaches - excedrine was much better.

Not long after that, I began having severe diarrhea. Twice I have had blood in my stool during these episodes. Thankfully, they do not come frequently.

When I got accepted into my doctoral program, I decided that I would do my best to stop my symptoms once and for all. My doctor tested my gallbladder (ultrasound and hida scan), my appendix (ultrasound), my ovaries (ultrasound), my liver functioning (blood test). After negative findings, I had a cat scan of my abdomen. Nothing was found. My doctor decided that it just must be IBS.

I moved to begin grad school and subsequently lost my health insurance (since I left my job). I am miserable. I want to feel normal again. I am always tired (which may be due to my lifestyle) and never feel normal. I am always queasy and constipated. I have never had normal periods and usually do not have any. In the last year, I have had 2 and they only last about a day.

I do not have health insurance, however, my university has a clinic that does not take insurance and the fees are minimal. If I get tested, I will do so through the university.

Does this sound like Celiac Disease? My grandmother and sister have hypothyroidism. Other than that, I do not believe that anyone has autoimmune diseases. I do not have a lot of money (I think grad students take a vow of poverty!) so I am trying to decide if I need to be tested.


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



Celiac.com Sponsor (A8-M):



mushroom Proficient

Hi, and welcome to the forum.

Yes, your history and symptoms sound like many of us on here; if you read around you will probably find your story many times over. The doctors all think of everything to test for but celiac disease. To rule that out (or in) what you need is a blood test consisting of the following:

Anti-Gliadin (AGA) IgA

Anti-Gliadin (AGA) IgG

Anti-Endomysial (EMA) IgA

Anti-Tissue Transglutaminase (tTG) IgA

Total Serum IgA

If this is positive they will probably recommend an endoscopy with biopsy checking for intestinal damage. I know you had an endoscopy but often the damage can only be seen under a microscope. You will find much discussion on here on whether or not the biopsy is really necessary, since that used to be the only way to diagnose celiac before the blood test was developed. There are many on here who have not even had the blood test, who just decided that gluten was their problem, found out it was, and could not bear the thought of going back on gluten fo 2-3 months to get tested.

Anyway, this is more than you need to know at this point, but you do need to get the blood test. Celiac is an autoimmune disease and celiacs often develop other autoimmune diseases, including hypothyroidism, so it is possible you have inherited the gene from your mother's side of the family.

Now, whether or not you wish to spend the money is your choice; you always can just try the diet and see if it works for you. There are many on here who are not happy without an official diagnosis, so it is strictly your choice. Just be aware that if the eliminate gluten and it helps you will not be happy about resuming eating it just to get tested because your reaction will likely be more severe.

Good luck on making a decision.

Archived

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

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

    • Total Members
      134,119
    • Most Online (within 30 mins)
      10,442

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

    • Total Topics
      121.7k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Russ H
      Hello, and welcome to the forum. Getting use to gluten-free eating is a struggle, but it is worth it. Your daughter should begin to feel much better and the fatigue will fade but it can take some time. I am sure you will get lots of suggestions from forum members - we have a few from the UK. I am a bit pushed for time just now but will come back later. Russ
    • Ginarwebb
      thank you so much for this information .. if I'm reading the results correctly I believe the range was  <15.0 Antibody not detected > or = 15.0 Antibody detected
    • coeliacmamma
      My 16 year old has just been diagnosed with coeliac, she loves food and is now struggling with the diet. She has a variety of different co editions and thos one just tops the list, she is a musical theatre student at college and loves what she does but fatigue gets in way alot of the time, are there any good amd tasty meals I can k make that will help?  Thanks for reading.
    • BelleDeJour
      Thank you so much @suek54 How are you doing today? I spoke too soon yesterday. Something (I can only think gluten-free sweets or a can of soft drink) set me off yesterday. Had a bath, applied some cream, still itching so applied some steroid and was awake until 3am. It's so frustrating. Always 2 steps forward, 1 step back. I am at work now and going to play it very much on the very safe side with food for the next few days.  My derm appointment is less than a week away. I will update on here because I do feel it important to help others. 
    • Scott Adams
      I’m sorry you’re going through all of this. It sounds very stressful, especially when you feel that your symptoms are not being taken seriously. Until you are seen next week, it may help to keep the focus very practical: take clear photos of the skin sores, write down a timeline of symptoms, list all medicines, eye drops, supplements, implants/leak history, and any test results, and bring that to the dermatologist. If there is drainage, spreading redness, fever, worsening pain, eye involvement, or signs of infection, that needs prompt medical care. I would be cautious about assuming parasites or staph without testing, and also cautious with new supplements or putting vitamin C directly on sores, since irritated skin can get worse. A dermatologist can culture lesions, biopsy if needed, and refer to infectious disease if the findings point that way. On the celiac side, I understand your concern for your son, but being HLA-DQ2 positive does not by itself mean he has celiac disease; it means he has a genetic risk. If he is eating gluten now, this is actually the best time for proper celiac blood testing before he tries a gluten-free diet. His symptoms, weight, congestion, and family history are worth discussing with a gastroenterologist, but he should not be told he has celiac based only on HLA status. For your own care, try to keep pushing for objective testing and clear documentation in your records, because that is often what gets doctors to take the next step.
×
×
  • Create New...