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

My Parents Tested Negative


cathzozo

Recommended Posts

cathzozo Apprentice

This is long, but please help...

I never had blood tests or stool tests and have been gluten-free since April. I originally went gluten-free to support my husband who we suspected might have a wheat allergy affecting his asthma. I babysit for an autistic boy so I had been following their Gluten-free Casein-free research for years, and I decided that if I was going to test wheat-free with my hubby, I might as well try gluten-free.

I immediately felt better. Chronic D became only intermittent. Less fatigue - measured by less afternoon naps. I often get home and think I need a nap out of habit, yet I don't actually fall asleep most days anymore. Previously, I slept for 60-90 minutes after getting home from work almost every day. My TSH level has been dropping into the low end of normal and my endocrinologist wants me to start dropping my synthroid dosage.

My parents were so impressed that they started to thinking about it and decided to get the full blood panel. Today they got their results back and both of them are negative. I was so sure my mom would be positive. Her family all has gastro issues and all of them (even her brother) are hypothyroid. I don't know the exact numbers, but my mom was a doctor herself and fully researched what tests they needed before hand.

Now I am totally doubting myself. Am I just imagining all of this. Or is it possible that this is some sort of wheat allergy and not a gluten problem? Should I do a gluten challenge? Should I get Enterolab testing? Or do I just go on with my current gluten-free diet and assume I am right? I was just set on the idea that my parents test were going to validate all of this work for me, but it hasn't seemed to work that way...

Thanks for any ideas/advice.


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



Celiac.com Sponsor (A8-M):



eKatherine Apprentice

Do you need a doctor's permission not to eat something that is clearly making you sick? Of course not. Don't worry about anything but staying healthy.

shayesmom Rookie
My parents were so impressed that they started to thinking about it and decided to get the full blood panel. Today they got their results back and both of them are negative. I was so sure my mom would be positive. Her family all has gastro issues and all of them (even her brother) are hypothyroid. I don't know the exact numbers, but my mom was a doctor herself and fully researched what tests they needed before hand.

Now I am totally doubting myself. Am I just imagining all of this. Or is it possible that this is some sort of wheat allergy and not a gluten problem? Should I do a gluten challenge? Should I get Enterolab testing? Or do I just go on with my current gluten-free diet and assume I am right? I was just set on the idea that my parents test were going to validate all of this work for me, but it hasn't seemed to work that way...

Thanks for any ideas/advice.

My mother has been going in for Celiac panels and endoscopies for over 9 years now and has yet to be diagnosed. She has the full battery of tests run every 2-3 years and has a colonoscopy every 2. Yet when she remains gluten-free, she "miraculously" does much better and can actually leave the house without planning her day around the presence/absence of public restrooms. But she of course hangs on to her test results to justify her cheating....and then complains of hearburn, reflux and insomnia. :huh:

My dd and I are both completely gluten-free and are doing incredibly well. Dd was tested (with negative blood results) and I never was as I voluntarily put myself on the diet just to see. Celiac or not....the fact is, we are gluten-intolerant/sensitive/allergic.....whatever it is....gluten doesn't work for us. And if either of us has so much as a crumb of gluten....some major problems hit immediately.

Don't doubt yourself on this. You know better than anyone how you feel. If you need further "proof", look into Enterolab. At least that will get you some real answers unlike the methods my mom is currently using to determine hers. I'm thinking that by the time she hits 15 years of GI issues, reflux, heartburn, insomnia, weight loss.....the damage should have progressed enough to be detectable by traditional means. And then she can start the diet while treating for osteoporosis. <_<

Oh! And FYI~ my mother's sister has been going into the doctor for GI problems and generalized ill health for 5 years now. When she first heard of what I was doing with Shaye in regards to the diet and all of the symptoms dd had shown....she said, "OMG! That is EXACTLY what I've been feeling". She was tested and has biopsy-proven Celiac Disease. You may find that your non-diagnosed observations and results will carry a long way in terms of helping other family members get to the bottom of their own health issues.

Guest nini

Celiac is only ONE of the many manifestations of gluten intolerance, when the Dr.s test for it they are ONLY looking for Celiac, so just because test results are "negative" it only means that they are "not positive for Celiac" at least according to the CURRENT diagnostic standards. No one needs permission from a Dr. to be on a gluten-free diet and positive dietary response like you've shown is more than sufficient evidence to stay gluten-free. My daughter's test results were also "negative" but mine were highly positive... go figure... my daughter still responded miraculously to the gluten-free diet and therefore is most definitely gluten intolerant. It doesn't matter what her "tests" say, her body tells her she can't have it and she is so much healthier without it. Admitedly it's harder to convince grown people to ignore the "tests" and to simply try the diet... "it couldn't be THAT simple!" uh yes it is... why make it more complicated than it has to be?

cathzozo Apprentice

Thank you all for your responses. I am feeling much better this morning than I was last night when I first heard the results from my parents. I have a habit of doubting myself and that definitely was a problem last night. Once my husband got home, his response was the same as all of your responses. More importantly, I was convinced that this was a solution before my parents ever considered the testing. If I *knew* this then, why am I doubting it now?

Originally last night, I spoke with my dad. He was the one who told me that the tests were negative. Later when I talked to my mom, I found out that she still plans to try gluten-free for at least 6 weeks to see if it affects her TSH. So even she isn't putting full faith into the blood tests.

Sometimes mood is much better and logic is much simpler in the morning light rather than evening sleepiness... :)

I appreciate all of the support from this board. It seems like the medical world has been really learning a lot about this in the last few years, but they still seem to be missing many things. And maybe those missing links are the explanation for me and my family.

Shayesmom - It's great that you were able to help your aunt by showing how it has helped you and your daughter. That's cool! I'm considering going with Enterolab, but I think doing that is an act of further self-doubt, so I will try to avoid that (except maybe fore testing other sensitivities).

eKatherine - This is somewhat embarrasing, but the truth is I already have my doctor's permission to eat gluten-free. She said that if I felt better that we wouldn't worry about the bloodwork. And that's my real doc. My doctor mom is very supportive.

nini - I must remember simple. I can certainly complicate anything. :)

So, with reminders that I still need to work on self-doubt, I will sign off and get to work. Have a great day!

jenvan Collaborator

cathzozo-

Yes, as has been said here, just b/c your parents don't have celiac disease, doesn't mean you can't. My parents both have other autoimmune conditions (my mom has Hashi's), but neither had positive bloodwork or biopsies...so don't let it throw you.

spunky Contributor

One reason I don't like doctors is that tthey are hung up on lab tests and other high-tech testing results, no matter what a person sees in his or her own life experience.

I agree with what so many others here have said, "You don't need a doctor's permission..."

There is no doubt in my mind that my health has vastly improved now, 8 months' gluten free, from where I was last January, when I really wondered if I was dying. I didn't consult a doctor, I just went gluten free to the extreme and hoped I would get better. I often wonder what a doctor would've told me if I'd gone back in January, and, while I know some people have been helped by doctors, from my own past experience with them, I'd be willing to bet I would still be sick and in the midst of all kinds of expensive, invasive lab work that would have them scratching their heads and calling me hypochondriac.

Trust yourself. If you are better, then you are obviously doing something right.


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor
Thank you all for your responses. I am feeling much better this morning than I was last night when I first heard the results from my parents. I have a habit of doubting myself and that definitely was a problem last night. Once my husband got home, his response was the same as all of your responses. More importantly, I was convinced that this was a solution before my parents ever considered the testing. If I *knew* this then, why am I doubting it now?

Originally last night, I spoke with my dad. He was the one who told me that the tests were negative. Later when I talked to my mom, I found out that she still plans to try gluten-free for at least 6 weeks to see if it affects her TSH. So even she isn't putting full faith into the blood tests.

Sometimes mood is much better and logic is much simpler in the morning light rather than evening sleepiness... :)

I appreciate all of the support from this board. It seems like the medical world has been really learning a lot about this in the last few years, but they still seem to be missing many things. And maybe those missing links are the explanation for me and my family.

Shayesmom - It's great that you were able to help your aunt by showing how it has helped you and your daughter. That's cool! I'm considering going with Enterolab, but I think doing that is an act of further self-doubt, so I will try to avoid that (except maybe fore testing other sensitivities).

eKatherine - This is somewhat embarrasing, but the truth is I already have my doctor's permission to eat gluten-free. She said that if I felt better that we wouldn't worry about the bloodwork. And that's my real doc. My doctor mom is very supportive.

nini - I must remember simple. I can certainly complicate anything. :)

So, with reminders that I still need to work on self-doubt, I will sign off and get to work. Have a great day!

I am glad to hear that if your Mom has problems she is going to try the diet anyway. I am the one who was always negative with blood tests in my family and it resulted in many misdiagnoses and years of pain. Everyone else showed up on the blood tests, even one family member who 'thought' he had no gluten issues, until they were gone. It is often helpful to get your hands on the actual test results also rather than just the doctors decision on them. At times a doctor will call a very low positive a negative or inconclusive result.

Guest ~jules~

Yep, autoimmune diseases run in my family also. I have a diabetic mother, and grandmother on that side. On my fathers side I have a grandmother who died of lymphoma when he was 6, she died 6 months after her mother died of the same thing. I don't suspect celiac symptomatically in any of my family, accept one. My oldest brother has DH (I don't even dare to try to spell it) he just dismisses it as skin problems! I really wish I knew more about food intollerances before celiac came to me. With all my illness, confusion, and researching on the net I never "clicked" on celiac or gave it a second read. It never even ran across my mind that I could be sick because of what I was eating.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,563
    • Most Online (within 30 mins)
      7,748

    Bob Madden
    Newest Member
    Bob Madden
    Joined

  • Celiac.com Sponsor (A20):



  • Celiac.com Sponsor (A22):




  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • Scott Adams
      Oats naturally contain a protein called avenin, which is similar to the gluten proteins found in wheat, barley, and rye. While avenin is generally considered safe for most people with celiac disease, some individuals, around 5-10% of celiacs, may also have sensitivity to avenin, leading to symptoms similar to gluten exposure. You may fall into this category, and eliminating them is the best way to figure this out. Some people substitute gluten-free quinoa flakes for oats if they want a hot cereal substitute. If you are interested in summaries of scientific publications on the topic of oats and celiac disease, we have an entire category dedicated to it which is here: https://www.celiac.com/celiac-disease/oats-and-celiac-disease-are-they-gluten-free/   
    • knitty kitty
    • knitty kitty
      Hi, @Ginger38, I've had shingles in the past.  I understand how miserable you're feeling.   Not only do i have the chickenpox virus lurking about, I also have the cold sore virus that occasionally flares with a huge cold sore on my lip when stressed or exposed to gluten.  The virus lives dormant in the nerves on the left side of my face.  It causes Bell's Palsy (resulting in drooling).  The cold sore virus is also in my eye.  My eye swells up and my vision is diminished permanently whenever I have a flare, so it's of the utmost importance to keep flares away and treat them immediately if they do happen so I don't lose any more vision.   I take the amino acid supplement L-Lysine.  Lysine messes with the replication of viruses, which helps the body fight them off.   I haven't had an outbreak for several years until this year when exceptionally stressed and contaminated, it flared up again. Lysine has been shown to be beneficial in suppression of viruses like the cold sore virus (a herpetic virus), the chickenpox virus (also a herpetic virus), as well as the HIV virus, and even the Covid virus.   I also take additional Thiamine in the form TTFD (tetrahydrofurfuryl disulfide) because Thiamine has antiviral properties as well.   For pain, a combination of Thiamine (like TTFD or Benfotiamine or Thiamine Hydrochloride), with B12 Cobalamine, and Pyridoxine B6 have been shown to have analgesic properties which relieve pain and neuropathy.    The combination of Thiamine B1, Pyridoxine B6 and Cobalamine B12 really does work to relieve pain.  I take it for back pain from crushed vertebrae in my back.  This combination also works on other pain and neuropathy.   I usually buy a supplement that combines all three and also Riboflavin B2 called EXPLUS online.  However, it's made in Japan and the price with the tariffs added makes it really expensive now.  But the combination of Thiamine B1, Pyridoxine B6 and B12 Cobalamine (and Riboflavin B2) still work even if taken separately.   I can't take Tylenol or ibuprofen because of stomach upsets.  But I can take the vitamin combination without side effects.  However, you can take the three vitamins at the same time as other pain relievers for added benefit.  The vitamins help other pain relievers work better. I hope you will try it.  Hopeful you'll feel better quickly. Interesting Reading: Thiamine, cobalamin, locally injected alone or combination for herpetic itching: a single-center randomized controlled trial https://pubmed.ncbi.nlm.nih.gov/23887347/ Mechanisms of action of vitamin B1 (thiamine), B6 (pyridoxine), and B12 (cobalamin) in pain: a narrative review https://pubmed.ncbi.nlm.nih.gov/35156556/ Analgesic and analgesia-potentiating action of B vitamins https://pubmed.ncbi.nlm.nih.gov/12799982/ A Narrative Review of Alternative Symptomatic Treatments for Herpes Simplex Virus https://pmc.ncbi.nlm.nih.gov/articles/PMC10301284/
    • Mari
      I think, after reading this, that you areso traumatized by not being able yo understand what your medical advisors have been  what medical conditions are that you would like to find a group of people who also feel traumatized who would agree with you and also support you. You are on a crusade much as the way the US Cabinet  official, the Health Director of our nation is in trying to change what he considers outdated and incorrect health advisories. He does not have the education, background or experience to be in the position he occupies and is not making beneficial decisions. That man suffered a terrible trauma early in his life when his father was assonated. We see now how he developed and worked himself into a powerful position.  Unless you are willing to take some advice or  are willing to use a few of the known methods of starting on a path to better health then not many of us on this Celiac Forum will be able to join you in a continuing series of complaints about medical advisors.    I am almost 90 years old. I am strictly gluten free. I use 2 herbs to help me stay as clear minded as possible. You are not wrong in complaining about medical practitioners. You might be more effective with a clearer mind, less anger and a more comfortable life if you would just try some of the suggestions offered by our fellow celiac volunteers.  
    • Jmartes71
      Thus has got to STOP , medical bit believing us! I literally went through 31 years thinking it was just a food allergy as its downplayed by medical if THEY weren't the ones who diagnosed us! Im positive for HLA-DQ2 which is first celiac patient per Iran and Turkey. Here in the States especially in Cali its why do you feel that way? Why do you think your celiac? Your not eating gluten so its something else.Medical caused me depression. I thought I was safe with my former pcp for 25 years considering i thought everything I went through and going through will be available when I get fired again for health. Health not write-ups my health always come back when you're better.Im not and being tossed away at no fault to my own other than shitty genes.I was denied disability because person said he didn't know how to classify me! I said Im celiac, i have ibs, hernia, sciatica, high blood pressure, in constant pain have skin and eye issues and menopause intensified everything. With that my celiac nightmare began to reprove my disregarded disease to a bunch of clowns who think they are my careteam when they said I didn't have...I feel Im still breathing so I can fight this so no body else has to deal with this nightmare. Starting over with " new care team" and waisting more time on why I think I am when diagnosed in 1994 before food eliminated from my diet. P.s everything i went through I did write to medical board, so pretty sure I will continue to have a hard time.
×
×
  • 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.