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

Am I Celiac?


jamrock

Recommended Posts

jamrock Rookie

In March 2006 I got very ill with some kind of virus which caused shortness of breath I was hospitalized for seven days, doctors thought pnuemonia, then PE then last of all asthma ( i am not asthmatic). They really werent sure what was wrong my ESR was 90 platelets eleveted and I was also anaemic. Things settled after then in June i became ill again this time it started with my feet swollen, then the next week came the skin rashes like allergy, then other parts of my body, fingers, face, hands, feet became swollen sometimes with rash sometimes without. I would get up each day wondering what area in my body would be swollen, then I had this constant shortness of breath and swelling in my stomach especially just after eating, by this I was hopitalized two more times. As the weeks progressed was now feeling pain in my bones, back joints, sometimes cramping im my stomach. As you can imagine I have seem numerous specilaists, rhuemotologist, haematologist, orthopedic surgeons, internist, herbalist, allergist and the list goes on.They even tried sending me to a psychiatrist (smile).

I did so much blood work, lupus test x4, xray, lung scan heart scan the works most came okay but the blood work showed that something was wrong, some autoimmune problem but which one, the doctors said that my body was fighting something.

Well i did the skin allergy test I reacted to almost everything I was now on a basic diet of mutton as the only meat and yam, breadfruit ( i am from the caribbean) but they were really "blaah" foods. I couldn't keep up with that anymore so I started trying some regular food. I started to get sick as you can imagine. I now said to myself okay this is definately a food allergy but which food? that was the question for days so I started to read and check the internet that is when i met the word gluten. I said okay let me try this gluten free thing for a couple of days that. Those couple of days is the best I felt in 10 months. But of course being the festive season and all I decided not to pass on the fruit cake as I wasn't too sure about this gluten thing anyway, needless to say my fingers and feet were swollen and so was my stomach.

I now wondered to myself after being ill for so many months and seen over 30 doctors locally and abroad why has no one made the connection between my shortness of breath, swelling in all parts of my body, rashes, bloating, joint and bone pains THAT I COULD BE ALLERGIC TO GLUTEN.

I printed some info on celiac disease and took it to my GP yesterday who said it is a possibly but it is rarely in black people. As I am not an expert at genes I requested a referal to a Gastroentrolgist where to get the necesaary test done.

I believe that this gluten allergy could be the answer to my problems. Guys what do you think?


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



Celiac.com Sponsor (A8-M):



emcmaster Collaborator

Hi there & welcome!

If you are feeling better without gluten, I'd say it is pretty certain that you have some sort of problem with gluten, whether it is celiac or gluten intolerance (some people believe they are the same thing - I'm one of them). I understand your frustration with doctors not knowing what it was. I'm glad you found it out on your own. Like you, I discovered it on my own, too.

The next step is whether you really want a diagnosis (with testing) or if you are content knowing that you are probably a celiac and need to stay away from gluten for life. Your doctor will probably be helpful.

Good luck!

jamrock Rookie
Hi there & welcome!

If you are feeling better without gluten, I'd say it is pretty certain that you have some sort of problem with gluten, whether it is celiac or gluten intolerance (some people believe they are the same thing - I'm one of them). I understand your frustration with doctors not knowing what it was. I'm glad you found it out on your own. Like you, I discovered it on my own, too.

The next step is whether you really want a diagnosis (with testing) or if you are content knowing that you are probably a celiac and need to stay away from gluten for life. Your doctor will probably be helpful.

Good luck!

Thanks for such a prompt response

I believe i will go ahead with the testing as I have four childen and my first a boy is 12 but pretty short for his age I am now concerned for him

Jestgar Rising Star

Hi Jamrock,

not sure what your ancestry is, but here is a study done in the US on "African-Americans" (which could be from anywhere) showing that Celiac does exist in the black population. Keep in mind that many of these people may have European genes as well, so not a perfect study.

Dig Dis Sci. 2006 May;51(5):1012-5. Epub 2006 Apr 27.

Celiac disease in African-Americans.

* Brar P,* Lee AR,* Lewis SK,* Bhagat G,* Green PH.

Department of Medicine, Columbia University College of Physicians and Surgeons, New York, New York, USA.

Celiac disease is generally under diagnosed in the United States and it is unclear whether the disease is encountered in ethnic minorities. Our purpose is to describe a case series of African-American patients with celiac disease. Nine (1.3%) African-American patients with celiac disease were identified from a prospectively generated database of 700 patients with biopsy proven celiac disease and seen between 1981 and 2004. Females predominated, with seven, compared to two males. Diarrhea was the presentation in only two patients, while three presented with iron deficiency anemia. One third had at least one autoimmune disease. Compliance with a gluten-free diet, the only medical therapy of this disease, was poor. Only four patients adhered strictly to the diet. Celiac disease occurs in African-Americans and may well be underdiagnosed. Special attention needs to be given to methods that encourage adherence to the diet in minority groups.

CarlaB Enthusiast

If you get completely better gluten-free, then I'd assume it's a gluten intolerance or celiac.

I have a gluten intolerance, but it's a symptom of Lyme Disease -- I did not get completely better gluten-free, but I felt somewhat better. I'm not suggesting it's Lyme Disease for you as I don't even know if you have ticks where you are, but just that if you don't get completely better going gluten-free, you might keep looking as your food sensitivities might be due to another problem in addition to gluten intolerance.

Jestgar Rising Star
I have a gluten intolerance, but it's a symptom of Lyme Disease --

How can you tell that it's a symptom of Lyme, and not in addition to Lyme?

CarlaB Enthusiast
How can you tell that it's a symptom of Lyme, and not in addition to Lyme?

Well, I guess I don't know for sure. I will only know when I get better from the Lyme. It seems to be the case. I find it suspicious that in the beginning I got glutened frequently and got sick for 8 days each time. I am very careful ... I haven't been glutened since July, and I find that suspicious. Can anyone be that perfect? I know I do not have celiac.

Also, I know that food and chemical sensitivities CAN be a symptom of Lyme. I have had Lyme for over 30 years, so it has basically affected every bodily system of mine, digestion included. Lyme can cause an autoimmune condition in the body. That along with the fact that I tested positive for casein intolerance, went casein free for six months, then added it back to my diet with no reaction whatsoever made me think the gluten intolerance is also probably because of the Lyme.

I will never go back to eating gluten all the time, as it's obviously a weakness in my system and Lyme is opportunistic ... but it would be nice to be able to eat out again without worrying about contamination.


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

Jestgar, I guess I really misstated ... I lost a year of treating my Lyme Disease because all the symptoms matched up with celiac. I got better at first going gluten-free, but the progress quickly stopped and I thought that it just takes time, be patient. Finally, I started looking for something else that may be causing me to be ill. I just wouldn't want someone else to wait that long to start looking for something else ... if they're making progress, yes, keep at it, but if not, then keep looking.

I'm only talking about people diagnosed by dietary response ... obviously if you had a positive biopsy or blood work, it's different. People who "only" have a gluten problem, generally get better gluten-free.

Jestgar Rising Star

I was just curious because I remember that your daughter was also investigating gluten as a possible issue.

I think all these auto-immune responses are just fascinating. It would be interesting to catalog all the different responses that are possible with all the different auto-immune illnesses and see which things are basically common to all of them and which (if any) are specific to each illness. I'll be interested to hear how treating your (and Rachel's) Lyme affects what your body does when you eat gluten. Maybe it really is a symptom....

it would be nice to be able to eat out again without worrying about contamination.

Boy, I here you there!

jamrock Rookie
Well, I guess I don't know for sure. I will only know when I get better from the Lyme. It seems to be the case. I find it suspicious that in the beginning I got glutened frequently and got sick for 8 days each time. I am very careful ... I haven't been glutened since July, and I find that suspicious. Can anyone be that perfect? I know I do not have celiac.

Also, I know that food and chemical sensitivities CAN be a symptom of Lyme. I have had Lyme for over 30 years, so it has basically affected every bodily system of mine, digestion included. Lyme can cause an autoimmune condition in the body. That along with the fact that I tested positive for casein intolerance, went casein free for six months, then added it back to my diet with no reaction whatsoever made me think the gluten intolerance is also probably because of the Lyme.

I will never go back to eating gluten all the time, as it's obviously a weakness in my system and Lyme is opportunistic ... but it would be nice to be able to eat out again without worrying about contamination.

How does one get tested for Lyme disease? Bloodwork?

CarlaB Enthusiast
I was just curious because I remember that your daughter was also investigating gluten as a possible issue.

I think all these auto-immune responses are just fascinating. It would be interesting to catalog all the different responses that are possible with all the different auto-immune illnesses and see which things are basically common to all of them and which (if any) are specific to each illness. I'll be interested to hear how treating your (and Rachel's) Lyme affects what your body does when you eat gluten. Maybe it really is a symptom....

Boy, I here you there!

My daughter who has been gluten-free for over six months is doing a gluten challenge to verify that gluten is a problem for her. We did not see the dietary response we expected from her going gluten-free, and she is not having any reaction at all (so far) to the gluten she's been eating. That is another thing that is making me think it's more of a symptom than anything for me. I KNOW I have reacted to it in the past, and I'm very curious to see how it works out in the future.

CarlaB Enthusiast
How does one get tested for Lyme disease? Bloodwork?

Yes, but the bloodwork is notoriously inaccurate ... Open Original Shared Link is the place most Lyme specialists trust. Do you have ticks where you are?

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. - Borky posted a topic in Dermatitis Herpetiformis
      0

      Gluten food test strips

    2. - Wheatwacked replied to Midwesteaglesfan's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Going for upper endoscopy today

    3. - Midwesteaglesfan posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Going for upper endoscopy today


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,268
    • Most Online (within 30 mins)
      7,748

    Cookie Monster13
    Newest Member
    Cookie Monster13
    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

    • Borky
      I just recently saw something on this.  Has anyone tried test strips?  Which brand is better?  Not sure how they really work and if they really do work.  Thank you, Nancy (aka Borky)
    • Wheatwacked
    • Wheatwacked
      Hello @Midwesteaglesfan and welcome. A result greater than 10 U/mL is considered positive. Some labs use 15 as the cutoff, but 34 is in the positive.  The endoscopy and biopsy is looking for damage to your small intestine.  I don't don't think 5 days is enough to repair the damage. This comment is effectly your answer, regardless of your biopsy results.  The endoscopy has been the Gold Standard diagnostic, and most healthcare providers won't diagnose celiac disease until your intestinal lining Marsh Score reaches stage 3. You don't really want to wait for the damage to get worse, especially since only five days mostly gluten free gave you relief.  Yes, migranes is one of the 200 symptoms that may be caused by Celiac Disease. Malabsorption Syndrome is often comorbid with celiac disease.  The western diet is deficient in many vitamins and minerals.  That's why gluten processed foods are fortified.  Gluten free processed foods are not; Vitamin D deficiency is a virtual given.  40 to 60% of the industrial population is deficient in vitamin D, Damage to the intestinal lining from celiac disease can decrease the number of vitamin D receptors.  So now you get no vitamin D from the sun (skin cancer scare) the major source of vitamin D, plus absorbtion from food is poor because of intestinal damage.   Low iodine intake is getting more of a concern because the major source of iodine used to be bread (dough conditioner with iodine was stopped in the US in the 1970s), dairy (lactose intolerance from eating quick pickles with vinegar instead of fermented pickles which supply lactase excreting lactobacillus to improve Lactose intolerance. Commercial Dairies have wheat, barley and rye added to the cow feed. Some say they are sensitive to milk protein, but it is the gluten added to supplement the cow feed to increase milk production that becomes part of the milk protein causing the problem.  And people use less iodized salt.  In the US intake of iodine dropped 50% from 1970 to 1984. Switch to Grass fed only milk and consider supplementing Liquid Iodine drops to your diet.  The omega 6 to omega 3 ratio of commercial milk is 5:1; Organic milk is 3:1 and grass fed milk is 1:1. The typical western diet is around 14:1, optimum for humans is 1:1.  Wheat flour is 22:1 omega 6:3.  Choose vegetables lower in omega 6, it is inflammatory. Eat fermented foods and switch to Grass fed only milk.  Some say they are sensitive to milk protein, but it is the gluten added to supplement the cow feed to increase milk production that becomes part of the milk protein.   
    • Midwesteaglesfan
      At 41 years old I have been fighting fatigue and joint pain for a couple months.  My family doctor kept saying nothing was wrong but I was insistent that I just didn’t feel right.  Finally after running several blood labs, one came back showing inflammation in my body and I was referred to a rheumatologist.  He was extremely thorough and sat with me and my family for a good hour asking questions and listening. He ordered X-rays of all my joints and more bloodwork.  He suspected some sort of reactive inflammatory arthritis.  My TTG (Tissue Transglutaminase) came back at 34. he told me to try going gluten free and out me on Salfasalzin to help the join inflammation.  Over the next couple days going gluten free and doing a lot of research and talking to people with celiacs,  we found that I should have an upper endoscopy for insurance purposes in the future.  I reached back out to my rheumatologist and expressed this concern and he got back to me stating I was correct and resume regular gluten diet and stop the medication until after that scope.     They were able to schedule me in for 2 days later.  I had been gluten free, or as close to it as I could be for about 5 days.  I know I ate some brats with it but wanted to use them up.  My symptoms had gotten slightly better in those 5 days.  I felt less fatigue and joint pain was slightly better(it had gotten really bad) so for these last 2 days I’ve gone crazy with wheat bread, pasta and such.  I’m hoping those 5 days didn’t screw this endoscopy up.  I can’t imagine after a life of gluten, my intestines healed in 5 days and after eating gluten again for these couple days,  my stomach hurts, joint pain is coming back up so I know the inflammation is there.   Hinesight after this diagnosis, I have had chronic migraines since my late teens.  Has that been a lingering symptom of celiacs all these years?  I’ve never really had the stomach issues, for me it came in heavy these last couple months as the fatigue, just always feeling tired and exhausted.  And the joint pain.     So getting in the car for the 2 hour drive to the hospital for this scope now.     Wish me luck!
    • marlene333
      To play it safe, use Vasoline Lip Therapy. No questions as to it containing gluten.
×
×
  • 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.