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

Living In Egypt

Knoppie

Recommended Posts

Knoppie Apprentice
Knoppie
Posted

I live in Egypt and have been having some of the symptoms of celiac disease. I recently found out that it runs in the family.

Here in Egypt, the blood test is unheard of but I read that you can do a stool exam and that it would show presence of fat cells right?

I want to know if I have to make sure that i eat enough fat to show on the test and when should I do it after I eat it? Also will it make a difference that I haven't had any gluten for 3 days?

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

Celiac.com Sponsor (A8-M):


ravenwoodglass Mentor
ravenwoodglass
Posted

It sounds like they are doing a stool test for malabsorption which would result in fat being present in higher than normal amounts. For that it wouldn't matter if you have been gluten-free for that short of a time. If you might be having an endoscopy done you need to make sure you are stay on gluten until that is done. Your doctor would be the best one to ask about the dietary requirements as far as what you are eating and when to test.

Knoppie Apprentice
Knoppie
Posted
  • Author
It sounds like they are doing a stool test for malabsorption which would result in fat being present in higher than normal amounts. For that it wouldn't matter if you have been gluten-free for that short of a time. If you might be having an endoscopy done you need to make sure you are stay on gluten until that is done. Your doctor would be the best one to ask about the dietary requirements as far as what you are eating and when to test.

The thing is that most doctors here aren't that great and I wouldn't really know which doctor to go to. Does the stool exam only test for malabsorption and not other things?

There isn't a lot of fat included in my diet, should I include fat before doing the exam or is it irrelevant?

  • 4 months later...
msharnoubi Newbie
msharnoubi
Posted
I live in Egypt and have been having some of the symptoms of celiac disease. I recently found out that it runs in the family.

Here in Egypt, the blood test is unheard of but I read that you can do a stool exam and that it would show presence of fat cells right?

I want to know if I have to make sure that i eat enough fat to show on the test and when should I do it after I eat it? Also will it make a difference that I haven't had any gluten for 3 days?

The blood tests are available in Egypt. You can do them at Open Original Shared Link

But you have to explicitly specifiy the names of the test, that is the exact name letter by letter. Don't tell them celiac tests, they'll probably won't know them and don't just say Igg for example or you may risk them doing you another Igg and not the anti-gliadin.

As for the doctors, I agree, it's difficult to find one who is competent in celiac (hope I'm wrong). But hopefully, they will catch on.

Good luck.

nora-n Rookie
nora-n
Posted

Researchers tested various people all around the mediteranean, and surprisingly many were positive when they ran the tissue transglutaminase IgA test (the usual screening test in europe)

I guess there are many many undiagnosed celiacs in egypt.

Can you order the findout celiac home test from europe? You do not need a doctor.

maybe your pharmacy can order it?

It is an Ttg IgA test.

There is also a variant that tests for IgA deficiency simultaniously, I think they have it in cananda or the u.s. , maybe it also does the IgG version, whatever.

the Ttg IgA test costs about 25 dollars here where I live. You take a drop of blood and do the test at home.

The stool test you can read about at the www.enterolab.com website. They both test for fat malabsorption and Ttg IgA in the stool (and will not pick up people with IgA deficiency) they also have he gene test. enterolab tests you do not need a docotr's oerders for.

nora

Archived

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

Go to topic listing
  • Celiac.com Sponsor (A19):


  • Member Statistics

    • Total Members
      131,951
    • Most Online (within 30 mins)
      7,748
    SY8
    Newest Member
    SY8
    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

    • Jacki Espo
      Covid caused reoccurrence of DH without eating gluten

      By Jacki Espo · Posted

      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
      New Celiac Mama in My 30s

      By Mari · Posted

      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
      My only proof

      By Mari · Posted

      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
      Does anyone here also have Afib

      By knitty kitty · Posted

      Fascinating.
    • DebJ14
      Does anyone here also have Afib

      By DebJ14 · Posted

×
×
  • 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.