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

Dylan C

Recommended Posts

Dylan C Newbie

So i am undiagnosed and have been having severe problems for about 9 months. Ive had stomach problems my whole life. i had a small part of my bowel removed when i was a newborn and had a colostomy bag for 6 months but recovered. I was always active as a child and teen but still had problems, but nothing like this. So now I'm 21 and one day i got really sick in a car and it all started from there! Got very dizzy and wanted to puke. But then i started to have abdominal pain, bloating and bad chest pain. I thought it was a bug and let it pass but it went on for weeks. Then i got constipation and started getting very fatigue and weak. Could barley got to work. One day at work i started having suck bad lower abdominal cramps that they wheeled me out on a cart because i could not walk. I went to the er that night after they went away but since then i have had a lot of symptoms. Mostly lower abdominal pain around my pelvis.( By the way I'm a 22 year old male) . But i have been having bad fatigue, arthritis in my fingers when i wake up, severe abdominal pain that only goes away on occasions, testicular tenderness mostly when I'm constipated, severe stress mostly because of my sickness, bad mouth ulcers, and I'm sure there is a lot of symptoms I'm missing but i have been to doctors and even had a colonoscopy which came back good but I've never been tested for celiac or crohns that i know of. Sometimes i really feel like i dying, the depression had led me to hate everything. I can't really enjoy my wife and kids anymore, can't go out anywhere and have fun because I'm always sick. Im going to see a new family doctor this thursday and try to get some test ran but does anybody have symptoms like me and does this sound like celiac? Help me please i just want my life back. Also i have recently gotten itchy bumps on my hands, wrists and inner forearms and on the right side of my neck( kinda like bug bites all over).


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



Celiac.com Sponsor (A8-M):



SLLRunner Enthusiast

Welcome, @Dylan C.

I am sorry you are not feeling well. There are over 300 symptoms of celiac, but with what you describe I'm surprised you have not been tested for that or chrons, especially as a child. When you go to the new doctor, be proactive and specifically tell them you want a referral to a GI and that you want to be tested for celiac and chrons.

Be sure to continue eating gluten until all testing is complete. 

cristiana Veteran

Hi Dylan

I just wanted to join SLLRunner in welcoming you to the forum and yes, do ask to be tested for Celiac and Chrons.

My nutritionalist told me that celiac disease is a great mimicker of many illnesses which I think must make a doctor's job all the harder when it comes to diagnosis.  For many of us it took us  a long time to get a diagnosis - for about eight years before my own diagnosis I had ulcers,  odd migraines and hallucinations on waking, anxiety, elevated blood protein but no obvious cause for it, anemia, numb hands and arms in the mornings, and eventually the abdominal pain and severe diarrhea. It was all scary stuff but  it was only when I got the last two symptoms, for six weeks, that I was tested for celiac disease (for the protocol here in the UK is that if you have a new gastric symptom for more than six weeks you should have further investigations).  I still wonder if I hadn't had that gastric pain and diarrhea whether my doctors would have even thought it was celiac related?

After all you have been through it is not surprising that you are feeling depressed.  A lot of people feel very depressed and anxious before their diagnosis.  You are doing the right thing seeing a new doctor, and hopefully you are just around the corner from getting some long awaited answers.  

Keep us posted.  You will find  some great advice here and support during your journey.  All the very best.

Ntf2001 Newbie

Sorry to hear you are in pain! If it makes you feel any better I am going through it too.  I'm a 25 yo female. It's been 5 months since symptoms,  issues my whole life. I'm pretty sure my primary doctor thinks I'm crazy.... 

Think of the positive.  You can't let your symptoms (even though they can be debilitating) rule your life.  Set little goals for the day - a 10 min walk or watch a show with your kids. Small steps.. It will get better :)

Sugarcube Rookie

You mention that you might have had a stomach bug at some stage?  So in addition to celiac, I would also suggest testing for giardia / other infections.

My Giardia had caused many of the symptoms (abdominal pain, nausea, constipation, loss of appetite, fatigue etc) that you mention.  Giardia can become chronic and may not clear itself without antibiotic treatment.

Awol cast iron stomach Experienced

I am still currently on the path of diagnosis too. We are not dying just have triggered the immune system into hypersensitivity even to our own self. You are not alone and I wish you a quick recovery and better health.

I'll share my story.  I have had issues all my life. I was constipated my whole life and had several issues over the years that someone should have questioned celiac all on the 300 list but I was not the typical original textbook type. I was however diagnosed IBS in my early 20s and told I had to figure out what I could and could not eat. Yep then sent on my way. Still on that mission. I actually went gluten-free three and a half years ago as the snowball of symptoms got worse. I know we are not supposed to go gluten-free without testing but I was done with Dr's. I complained of more issues and my wonderful husband in lay terms said bread is bad for you. I see it when I look at you- just stop bread. I did and in the first two weeks I knew he was right and IBS was wrong. I was wheat allergy, NCGS, or Celiac. I didn't care which one I went gluten-free . Overall things were fantastic then 3 1/2 years into my new found pain free regular bowel life I got glutened 2x in the same month. I still have not recovered from restaurant/ catered party food. I emailed and called ahead to state gluten-free food needed etc my hostess' both knew i ate gluten-free. It hit me worse than before when I was still eating gluten. I had all my old symptoms and then some too many to list. this time New for me elbow joint pain was off the charts I had no comfortable position for my arms where my elbows did not hurt got 2 months. Then I knew I was celiac. I am finally seeing someone who might actually get it right this time. I have discovered keeping my newest food diary I can't have casein or coffee cross reactive molecularly I believe in my case. I refuse to eat gluten for testing I told them if they ask/make me I will lie. Not sure what they will say next, I have 2 more upcoming appointments. I am on this path only for my kids sake. I know -that's what is most important. All DR' s before the three most recent I crossed path with missed it, some members of my extended family did not believe me and constantly tried to get me to eat gluten because self diagnosing is not respected by them. Only my husband and cousin believe me. My husband can tell by just knowing and seeing me. My cousin is celiac I have not seen her in a few years and did not know the details of her symptoms/ diagnosis. She said I didn't know you were having problems go to message boards or social media the symptoms you described are there. So here I am on the path with you. To our health and well being.

Dylan C Newbie

Thankyou everyone for the comments. I hope all of you are well or on the right path! But one of my concerns is that I've not noticed that gluten make me sick. And this week I have felt pretty good. Just kinda out of energy but no pain. But I haven't felt my normal symptoms since I got this rash on my hands, wrists and neck. It's itches but it's weird that I haven't had pain. Did any of you have your good weeks? .. Oh and this isn't the first goodness I've had, I get one about every 2 months. 


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



Celiac.com Sponsor (A8-M):



Jmg Mentor
 

  But one of my concerns is that I've not noticed that gluten make me sick.

Neither did I for many, many years. It was only after going off it that I realised just how sick I was. A lot of what I'd accepted as normal (for me) turned out to be anything but. Some similar to you, abdominal pains, chest pains, bloating, low energy etc.  Lot's more too. Things which I'd lived with for so long that I no longer thought of them as remarkable. One reason 80% of coeliacs are undiagnosed is that it can present in so many different ways, sometimes with no symptoms at all. 

 

 

  Did any of you have your good weeks? 

Yes, 

Bottom line, don't exclude it till they've tested, it's important to find out what is causing your issues and if you go gluten-free the tests won't be conclusive. After that, even if they exclude celiac, give a gluten-free diet a try, keep a food diary and see if gluten, or dairy etc may be a problem. 

Best of luck!

Jmg Mentor
 

I am still currently on the path of diagnosis too.

Awol, why not post your comment in a new thread? You can get a lot of support and good advice on this board but I'm worried your post will get lost in Dylan's thread :)

Best of luck to you also btw! 

Awol cast iron stomach Experienced

Thank you JMG I will take your advice. I have not felt supported which is why my cousin told me to seek the experts- you. It has been 4 decades of misdiagnosis. Too long.

cyclinglady Grand Master

Dylan,

These are the specific tests for celiac disease.  You should try to ask for them all, if possible.  For a while, the TTG tests were considered the best for screening.  They are very good but do not catch all celiacs (like me).  Funny thing is that the University of Chicago used to recommend the TTG for screening (along with American GI Association).  With their new website re-vamp, they have included all the celiac tests.  Guess they figured that it is not all "one size fits all".  Remember, you only need one positive on the panel for your GI to do further investigation (e.g. endoscopy/biopsies).  

Open Original Shared Link

I wish you well!

Dylan C Newbie

So I had the celiac blood test yeaturday and also more ford allergy blood tests . And some other tests. Hoping for answers:)

Jmg Mentor
 

So I had the celiac blood test yeaturday and also more ford allergy blood tests . And some other tests. Hoping for answers:)

Good luck! Remember not to cut gluten just yet, there may be more tests ahead. You could start a food diary though, just note what you eat and how you feel. 

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 Jmartes71's topic in Related Issues & Disorders
      14

      My only proof

    2. - Jmartes71 replied to Jmartes71's topic in Related Issues & Disorders
      14

      My only proof

    3. - marion wheaton posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Are Lindt chocolate balls gluten free?

    4. - Dorothy O. commented on Scott Adams's article in Latest Research
      7

      Study Estimates the Costs of Delayed Celiac Disease Diagnosis (+Video)

    5. - JoJo0611 replied to JoJo0611's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      CT with contrast.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,404
    • Most Online (within 30 mins)
      7,748

    Starr98
    Newest Member
    Starr98
    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

    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
    • marion wheaton
      Wondering if anyone knows whether Lindt chocolate balls are gluten free. The Lindt Canadian website says yes but the Lindt USA website says no. The information is a bit confusing.
    • JoJo0611
      I didn’t know there were different types of CT. I’m not sure which I had. It just said CT scan with contrast. 
    • Scott Adams
×
×
  • 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.