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

Do I Have Cd?


Schnee0

Recommended Posts

Schnee0 Newbie

Hello,

I stumbled upon these forums from Google. I have been wanting to hear some input from people with celiac disease, and I am very happy to have found these forums.

I a 17 years old (Male) who thinks that he might have celiac disease.

All throughout my life, since I can remember at age 4, I have never always had normal stools.

At age 12 I was diagnosed with lactose intolerance. Thankfully, after cutting away all diary I was no longer having problems. Probably around September 2003 I could no longer have any diary at all, before I used to take lactaid pills, now even those do not work. Then, probably since October 2003 I have had various types of stools; some diarrhea, some constipation, some normal. I was still able to function and pulled through it. In February I just got tired of it, and that is when my mother suggested taking Metamucil and that helped relieve the diarrhea. Another thing to note: From Oct 03 to today I have probably never had consistent stools every day, it was more like every two days. I was used to these symptoms by now (due to my lactose intolerance), also I was never alarmed or felt like something was wrong because it is supposed to be a family thing. Probably both sides of my family have had various gastrointestinal issues, my dad's side of the family calls it "The Family Curse". Well I hate the curse!

Now in March I was really fed up with my guts, the metamucil stopped working and the diarrhea came back. Ever since then I have been trying to figure out what could be causing this trouble that I am having.

Here are my symptoms:

Weakness

Fatigue

Diarrhea

Random stomach/intestinal pain

Whenever I use the bathroom it feels like I still have to go, there is no "ahh now my pants fit better factor" :D

Unusually smelly farts/poop (sorry for putting it so literally)

Farting more than usual

My intestines feel like there are minor knife cuts all throughout them and for some reason they refuse to heal

Whenever I wake up in the morning I get the feeling from my guts that within two hours I will need to use the bathroom, I also usually have pain in my guts that goes away within 3 hrs.

Another thing to note: My symptoms that I am having now are a heck of a lot different then my lactose intolerance symptoms

Last week I started googling stuff, and some of my first results were websites related to Gluten. I saw the symptoms and they were exactly the same that I am having now! My nearest insurance certified doctor is over an hour away and I cannot travel in this condition, so just last week I visited my local doctor and without me asking any questions or suggesting what I might have he suggested that I might have a fructose or gluten problem. That further reassured my thoughts. My town is a commuter town, its biggest attraction is a movie theater, it is impossible for me to get a gastrointelolgist here, and the local doctor does not have the tools needed to perform accurate gluten/celiac disease tests.

Does anyone think I might have celiac disease?

I would like to go Gluten Free (even though many websites say not to do it until recommended by a doctor) and see if it helps.

Thanks,

Schnee


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



Celiac.com Sponsor (A8-M):



wwebby Apprentice

Hi Schnee,

I haven't been to my gastro yet either, but I finally made an appointment...If you're having trouble getting a doctor, you can order some tests yourself, but it does cost money. Many people here have done that same.

www.enterolab.com

Dr. Fine is a board-certified, though somewhat controversial, gastroenterologist and researcher who can do labs on you with your stool without a doctor's referral. You can order the tests yourself. The complete stool panel is $349, though if you want to go cheaper, you could get the gluten sensitivity test, which will tell you your IgA Anti-gliadin level for $99 and the tissue transglutiminase test for $99. If both are positive, I'd say, go gluten free and monitor your symptoms. Some people think his tests are not reliable, other people swear by them. I had them done myself and it was painless and easy and I think he might be on to something because even tho' the usual tests arent' through the stool, a new study just came out on some italian researchers that are starting to do the same thing.

www.yorkallergyusa.com

I just ordered this one...it's called CDScan and it's a finger-prick blood test you can order yourself for $99. It also tests for tissue transglutiminase, but through the blood, which is one of the standard ways they test you when you get a Celiac panel of blood tests at the regular doctor. I haven't gotten my results yet, but there's a review of test process that another celiac posted on www.celiacsanctuary.com if youwant to see pictures and all that.

The "official" diagnosis of celiac disease is when they put a tube into your small intestine, and take a couple snips of tissue and examine them under a microscope for damage. However, some people feel they can "self-diagnose" by going gluten free themselves and monitoring for symptoms, or getting some of the tests I mentioned above, going gluten free, and monitoring for symptoms.

If you do get any tests, don't go off gluten yet. The tests are more accurate if you are eating gluten. If you do get to an "official" doctor for testing, don't go gluten free. Not yet at least. If you go gluten free and your symptoms abate, but then you want testing done, you'll have to go back on gluten for a number of weeks to get accurate results. Stinks, doesn't it.

Good luck in your quest!

Stay healthy,

Laura in CT

wwebby Apprentice

You know Schnee, I just thought of another thing. Your local doctor should be able to help you out more. All your local doctor has to do is take some of your blood and then have it sent to a specialized celiac disease lab. I would think that just about any local doctor can draw your blood for testing???

Good labs for celiac disease testing are

Prometheus Labs

Specialty Labs

IMMCO Diagnostics

Mayo Clinic.

I know most of the labs will mail a collection kit and instructions to your doctor.

Hope this info helps.

--Laura in CT

  • 1 month later...
celiac3270 Collaborator

Hi,

First off, you can't know for sure if you're Celiac unless you get the blood test or, preferably, the endocopy. If you're going to get tested for that, keep eating the regular stuff that you feel could be giving you all these symptoms. However, if you aren't going to get tested, there's nothing wrong with a gluten-free diet. If it relieves your symptoms, then it doesn't even matter if you're Celiac or not...the diet makes you feel better.

As for symptoms, some of those sound very familiar. My primary complaint was the horrible stomach cramps, often usually with vomiting, that gave me so much trouble and pain. Since first grade (I'm now 13), I had been sick ALL the time. In first grade, I would eat dinner, then feel really sick, run to the bathroom, throw up, and then feel better. Later, it became once every week, or so, I'd get sick and have a 24 hour bout with this. Other symptoms included: severe bloating, occasional diarrhea (sometimes formed stools, sometimes loose), and rather stinky gas/stools. I never experienced fatigue, personally, but realize that it's a common symptom in Celiacs. In addition, I have never been extremely puny, but in basketball games and other contact sports, it's easy for me to be pushed around.

If you choose to start the gluten-free diet without first testing, keep in mind that your symptoms won't go away immediately (if you indeed have Celiac). I've been on the diet for 13 weeks and though my symptoms aren't as bad (knock on wood), they aren't perfect, either. Anyway, if you try the gluten-free diet, be patient, give it a few months, and make sure that you are 100% gluten-free or you won't feel any different. I believe there is a good list on this website of ingredients that are/aren't gluten-free. It's not just wheat, barley, and rye: there are a lot of ingredients to check for in each product and you'll find yourself making a lot of phone calls (because natural/artificial flavors may or may not have gluten). In addition, if you choose to stray beyond the simple meats, potatoes, vegetables, and other things that you can buy in your grocery store, there'll be some added expense. Good luck.

  • 11 months later...
Guest Doct.Giggles

I found a website in the Celiac.com website. It talks about the disease. https://www.celiac.com/st_main.html?p_catid...-08105001018.b0 check it out! :rolleyes:

-Tiffany

watkinson Apprentice

Hi Schnee,

It sounds like classic celiacs to me. <_<

If you do get tested, please understand that you have to presently be eating gluten for the blood test to come out positive.

If you decide to go gluten free (gluten-free) without the test, make sure everything is truly gluten-free.

You mentioned Meticmucil. I also take it, even though I have no more intestinal problems since going gluten-free. I take it for added intestinenal health. I use the regular formula because the sugar free kind has aspertame. One time I ran out and went to Target to get more. All they had in stock was the Target brand, so I bought it. For the next 6 weeks I kept feeling sick. Many of the same problems were coming back, like the numbness in my hands, extreme achiness, sleeplessness, and my stomach just not feeling right. It never accured to me to check the ingredients of the metimucil. I dont know why but for some reason one night I did. It was sugar free, had aspertame, and believe it or not, Maltodestrin containing gluten. :blink: obviously I stopped that night, and of course by the next day I felt fine.

Also be aware that foods that say "wheat free" or "no gluten added'" are not always gluten free. :(

I hope you start to feel better soon. Keep checking out this site for more information.

Wendy

  • 1 month later...
angellove839 Rookie

The blood test proved negative for me when I was having the exact same symptoms as you. The blood test does not work well unless you already have significant damage to your body so much that it is indicated in your blood stream. I'm 18 and I just got tested this month by Enerolabs with a stool test and I am positive for Celiac. I have been on the diet for 4 weeks now and except for the occasional wheat contamination, I am feeling much better. Definitely go with a stool test. It is painless and you just mail it out.


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:
    Donate

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,959
    • Most Online (within 30 mins)
      7,748

    jenny44
    Newest Member
    jenny44
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.