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

Husband Is Negative Too... Im So Confused


girlfromclare

Recommended Posts

girlfromclare Apprentice

Hubbie came back with negative blood results today. I didnt know whether to laugh or cry! So I cried.

Our son was also negative a few days ago and I was depending on hubbies results being positive to confirm hereditary celiac disease. Now we are left no clearer as to what to do. Anyway, we have started the diet. The bread is horrendous! So we are striving to make our own and it isnt too bad. Now that they are both negative though, neither are too keen on the diet. I dont blame them... but I am still inclined to think it would help. So they have agreed to stick to it for a couple of months perhaps. If there is no clear improvement in either of them, then I guess thats that!

I feel so disillusioned. I was so sure that they were both going to be testing extremely positively for celiac disease.

They are both clear candidates. I know that there are plenty of people in this group who have gone on positive dietry response alone, and I am perfectly happy to do that. but its hard to explain to other people namely family... you know the score!! Also, a few members of husbands family have similar symptoms and more... I was hoping that a positive diagnosis would convince them to get tested themselves! Oh Well.

Sorry for ranting. Im so disappointed.

Fingers crossed for improvements on the diet anyway!! I will stick to the diet if it works, no matter what anyone says.. but it would have been nice to have the medical confirmation! WHy do we all feel we need that???

Best of luck to everyone on the board.

Kind regards

Liz.


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



Celiac.com Sponsor (A8-M):



Guest nini

the blood tests can be false negative... it's possible if they were to have a biopsy (WHILE STILL CONSUMING GLUTEN) that they MIGHT pop positive on that... however, even that can be hit or miss, so trying the diet is your best bet...

Have you tried EnerG's Light Tapioca Loaf bread yet???? If you've tried anything else I can understand their dissappointment, but my daughter and I recently discovered this bread and we love it! With just a little warming in the microwave to soften it up (about 20 second or more) I've successfully made all kinds of sandwiches with it now and am in love with this bread. It's the closest thing to a WHITE BREAD flavor and texture that we have found. Now, it doesn't taste THAT great right out of the package, you do have to warm it in the microwave (as with most gluten-free breads) in order for it to be palatable, but once you warm it you can make sandwiches with it and put them in sandwich baggies for lunches or eat them right away.

girlfromclare Apprentice
the blood tests can be false negative... it's possible if they were to have a biopsy (WHILE STILL CONSUMING GLUTEN) that they MIGHT pop positive on that... however, even that can be hit or miss, so trying the diet is your best bet...

Have you tried EnerG's Light Tapioca Loaf bread yet???? If you've tried anything else I can understand their dissappointment, but my daughter and I recently discovered this bread and we love it! With just a little warming in the microwave to soften it up (about 20 second or more) I've successfully made all kinds of sandwiches with it now and am in love with this bread. It's the closest thing to a WHITE BREAD flavor and texture that we have found. Now, it doesn't taste THAT great right out of the package, you do have to warm it in the microwave (as with most gluten-free breads) in order for it to be palatable, but once you warm it you can make sandwiches with it and put them in sandwich baggies for lunches or eat them right away.

HI nini... thanks so much for that. You know I didnt know about putting it in the microwave. All the breads have tasted so dry and crumbly... really horrible. .. like old dried up madiera cake - but without the sweet taste. You can imagine my four year olds disappointment to find this in his lunch box at school! I baked some bread today that hasnt turned out too bad and if it gets dry overnight Ill pop it in microwave tomorrow. I just hope I can keep up the baking... its tough to fit everything in isnt it?

Im kind of thinking getting the celiac home testing kit... cheap price and only takes 10 minutes.... dont think it will be any more sensitive than what they doc would do though so probably get another negative there!

Anyway, all the best and thanks again.

Liz

kimber Enthusiast

I haven't even had dd/ds tested

We have a family history and their reaction to the gluten-free diet was enough for me

I can understand your wanting confirmation though

Good Luck

gluten-free bread is tough...my ds loves enjoy life white rice...I toast it and put on a little jelly

Kim

HI nini... thanks so much for that. You know I didnt know about putting it in the microwave. All the breads have tasted so dry and crumbly... really horrible. .. like old dried up madiera cake - but without the sweet taste. You can imagine my four year olds disappointment to find this in his lunch box at school! I baked some bread today that hasnt turned out too bad and if it gets dry overnight Ill pop it in microwave tomorrow. I just hope I can keep up the baking... its tough to fit everything in isnt it?

Im kind of thinking getting the celiac home testing kit... cheap price and only takes 10 minutes.... dont think it will be any more sensitive than what they doc would do though so probably get another negative there!

Anyway, all the best and thanks again.

Liz

vampella Contributor

Bread is interesting that's for sure!!! I have a 3.5 yr old Emmah who was diagnosed through diet. When I told the teachers they said ok and a week later they asked how she was Dx'ed....I just said blood work. They really do not need to know. Aside from other celiac's, just regular people I say bloodwork. it's really not ther business, is it?

I've tried a ton of breads. I've tried hommade and store bought, I've only been doing this a month so I haven't mastered the bread baking. the bread that Emmah seems to like the best I get at safeway. kinikinick (SP?) tapioca bread.

I have a check up today to see how Emmah's doing and I spoke to her doc on the phone last week. He doesn't know why she had 2 FALSE Neg tests. I did tell him I wanted an IgA test run to see if that was low because that can cause FALSE NEGS. Which I didn't know at the time. Here my doc only ran the TTG and that was it, it's all they are supposed to do here now. So today we are doing more blood work. That IgA will be run and I don't hope it's low but it would explain why it was meg. REMEMBER though..like my DR told us, NO test is 100%.

Good luck with the diet.

Like Liz said though put it in the micro. I also have to watch the thickness of the crust because some the crust is thicker and hard and Emmah's not a fan of that.

It's all trial and error. There are some great recipe books for bread also.

The Gluten-Free Gourmet Bakes Bread: More Than 200 Wheat-Free Recipes

by:

Hagman, Bette

Green, Peter H. R.

Char

kbtoyssni Contributor

There are a lot of bad gluten-free foods out there, but there are also a lot of good ones. I've had some really horrible bread, but now I eat Food For Life brand (my favorite are the black rice, red rice and millet). If you can try a different brand, I'd do that.

As for the negative test results, false negatives are not all the uncommon. If you would like a medical diagnosis, you could try gene testing through enterolab.

happygirl Collaborator

If you live near a whole foods, try their pizza crusts. I just moved to a larger area where there are WF and I am in absolute heaven. I have made pizzas and breadsticks...my non-gluten free parents even ate it and LOVED it. I highly recommend it if you are near one.

I have made the bob's red mill bread and enjoyed it. I also like some of the knnickinick (sp?) products.

but, by far, my most favorite is the whole foods pizza crust.


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



Celiac.com Sponsor (A8-M):



lonewolf Collaborator

All four of my kids tested negative, but the doctor and I agreed that one son should try gluten-free anyway. He has had great results. My oldest daughter decided on her own that going gluten-free made her feel better (she was 14, a bit older than your little guy) and is happily gluten-free without a diagnosis. The other two really don't show any symptoms, so they are allowed to eat gluten outside the house.

There are two threads going in the Coping with Celiac section that deal with this kind of thing. One is called something like "Not Truly Celiac" and the other "Do any Celiacs get offended..." You might find some helpful information there.

As for bread, either homemade, if you have a good recipe, Gluten Free Pantry Country French mix or Ener-G Light Tapioca are the best that I've found.

Nic Collaborator

I read an article on line where they were talking about testing methods for Celiac. They were quoting Dr. Fine and they said that the blood work is only about 60% accurate when it comes up negative. Could that really be? So for all of our kids who test negative there is still a 40% chance they really have it. That is a big percentage. Please correct me if anyone else read that article and I misread it.

Nicole

Nikki2003 Contributor
Hubbie came back with negative blood results today. I didnt know whether to laugh or cry! So I cried.

Our son was also negative a few days ago and I was depending on hubbies results being positive to confirm hereditary celiac disease. Now we are left no clearer as to what to do. Anyway, we have started the diet. The bread is horrendous! So we are striving to make our own and it isnt too bad. Now that they are both negative though, neither are too keen on the diet. I dont blame them... but I am still inclined to think it would help. So they have agreed to stick to it for a couple of months perhaps. If there is no clear improvement in either of them, then I guess thats that!

I feel so disillusioned. I was so sure that they were both going to be testing extremely positively for celiac disease.

They are both clear candidates. I know that there are plenty of people in this group who have gone on positive dietry response alone, and I am perfectly happy to do that. but its hard to explain to other people namely family... you know the score!! Also, a few members of husbands family have similar symptoms and more... I was hoping that a positive diagnosis would convince them to get tested themselves! Oh Well.

Sorry for ranting. Im so disappointed.

Fingers crossed for improvements on the diet anyway!! I will stick to the diet if it works, no matter what anyone says.. but it would have been nice to have the medical confirmation! WHy do we all feel we need that???

Best of luck to everyone on the board.

Kind regards

Liz.

Me and my husbands blood work came back neg and both are daughters have it.

Celina

IrishKelly Contributor
Hubbie came back with negative blood results today. I didnt know whether to laugh or cry! So I cried.

Our son was also negative a few days ago and I was depending on hubbies results being positive to confirm hereditary celiac disease. Now we are left no clearer as to what to do. Anyway, we have started the diet. The bread is horrendous! So we are striving to make our own and it isnt too bad. Now that they are both negative though, neither are too keen on the diet. I dont blame them... but I am still inclined to think it would help. So they have agreed to stick to it for a couple of months perhaps. If there is no clear improvement in either of them, then I guess thats that!

I feel so disillusioned. I was so sure that they were both going to be testing extremely positively for celiac disease.

They are both clear candidates. I know that there are plenty of people in this group who have gone on positive dietry response alone, and I am perfectly happy to do that. but its hard to explain to other people namely family... you know the score!! Also, a few members of husbands family have similar symptoms and more... I was hoping that a positive diagnosis would convince them to get tested themselves! Oh Well.

Sorry for ranting. Im so disappointed.

Fingers crossed for improvements on the diet anyway!! I will stick to the diet if it works, no matter what anyone says.. but it would have been nice to have the medical confirmation! WHy do we all feel we need that???

Best of luck to everyone on the board.

Kind regards

Liz.

My whole family came back negative (myself, my father, and my niece included), however, the diet is the only thing that did prove all the dr.'s wrong, sorry to hear that your family members seem to feel that dr.'s know everything...after they've been somewhat sick for long enough they may come to a different realization ;)

girlfromclare Apprentice

thanks so much everyone for your replies. Esp all the bread info! I have been checking it all out. Because we live in rural Ireland, our only heatlh food shop is forty minutes away and doesnt have a great deal of selection. There is a chain store about an hour away (tescos) who have a reasonably good range but its mostly own brand stuff. I didnt see any of the names you guys mentioned. But I am baking away anyway for the time being. Its not too bad. If the results are good then it speaks for itself really doesnt it? Actually, can anyone tell me what they substitute for sausages? I noticed that all the shops Ive checked out only have regular sausages. Even the meat substitutes sausages have wheat flour in them... My boy and hubbie love their sausages! Bangers and mash is a big favourite in our house..

Thanks again for all your help and advice. This is a fantastic place to come!!

Love Liz

x x

Nancym Enthusiast

The blood test is very flawed. It doesn't catch celiac when someone has the skin manifestation or the brain manifestations, generally. If you all feel like you need the paper to confirm it, try getting tested by Enterolab.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,964
    • Most Online (within 30 mins)
      7,748

    Cbear
    Newest Member
    Cbear
    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.