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

Testing Of Family


laurelfla

Recommended Posts

laurelfla Enthusiast

ok, so here's the deal. i was diagnosed this August, so my sister got tested and she's been diagnosed about a month. my dad just went to the dr. to get tested and he told my parents they probably both had the recessive gene for Celiac, which is why both their daughters developed it. oddly enough, the doc wasn't interested in doing bloodwork -- just went straight to the biopsy. we don't have the results of that back yet. what i am wondering is why he'd refuse to test my mom? i mean, i don't think he's openly refused but he said that she did not need to get tested. neither one of my parents has symptoms. i mean, my dad has had a lot of back/disc problems but nothing digestive or emotional or anything that would really suggest Celiac. is the dr. justified in deciding that my mom doesn't need to get tested? and if my dad does have it, does that mean she probably doesn't? i'm super confused and would appreciate any insights! :D


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



Celiac.com Sponsor (A8-M):



Rachel--24 Collaborator

I think both your mom and dad should be tested...period. I dont know why the doctor would be unwilling to test her. <_<

You dont have to have symptoms to have celiac but maybe this doctor is unaware of that fact. :huh:

Matilda Enthusiast

...

bluelotus Contributor

I am so glad you reiterated that, Matilda!! I have posted that fact about celiac disease's inheritance several times and in several relevant forums, but people just ignore it....

You, laurelfla, are lucky that your family wants to be tested, that they love themselves and you enough to wish for everyone's health. My dad and the rest of my family ignore the issue entirely, though everyone in his family seems to have relevant symptoms...... It is so frustrating. Then again, if one wants to die of cancer or some other messed up disease, I guess one has the right. I just find my dad's lack of interest disrespectful in many ways - to me, to any of my potential children or his grandchildren, to himself, to the rest of his family. So annoyed with this now, going to have to stop talking about it.

Wish your family luck, laurelfla.

cornbread Explorer

bluelotus, I hear you. Thankfully my mother was cool about testing (thankfully because her test was positive), and my dad was eventually talked into it (just to get me off his back I think!), but my other relatives (who actually have LOADS of symptoms... more than my parents) are totally in denial. They are "too busy" to get tested. Hello? Enterolab tests from stool samples - you're too busy to poop into a box?! :lol: I think it's denial. But, like you, I find their disinterest disrespectful. It's like they're not taking my condition seriously. People are always "I didn't know you were ill before?" Yeah, well maybe it's because I'm not a whiner, or because problems like depression, brain fog, chronic fatigue and nausea are invisible. People ask how you're feeling, you usually say "fine, thanks", you know? :rolleyes: Gluten had been effecting my health, mood and personality for 13 years - it pretty much *was* my personality. It kicked in when I was 17, so all my adult life people have just thought I was short-tempered and weak-stomached (which wasn't considered an illness since it "runs in the family...") ;)

bluelotus Contributor

Thanks for the response, Cornbread. I also get that "I never knew you were sick before" from my family. Yeahhhhhh....right. 1) You all don't live with me 2) Your body builds up a tolerance and most undxd celiacs don't have symptoms (at least not that are apparent or directly related)...... So frustrating.

laurelfla Enthusiast

thank you all for your responses!

i had no idea that the whole recessive/dominant gene thing was not in operation with celiac. i'll definitely pass on the information. i had not realized how very lucky i am that my family has been so supportive. my sister actually got her biopsy report back yesterday and her villi were super damaged. :( i think she's kind of upset about that, but then i think we're all familiar with that process! thanksgiving is going to be interesting, with all the explanation to relatives, but at least i am not alone, although i never would have wished this on anybody else in my family. the doc put my dad on the diet while we wait on the results come back, maybe in a couple of weeks or so.

i told my sister about the forum, but she doesn't really like computers or technology, so... :( i don't know what i would have done without you all!!


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



Celiac.com Sponsor (A8-M):



Jenn2005 Contributor

Laurelfla - I noticed you are from Gainsville. Can you tell me what doctor you see there? I am from Fort Pierce about 3 1/2 - 4 hours south but we are seeing a doctor in Gainsville at Shands. Just curious because we are not having a lot of luck with the doctor we are seeing.

Jennifer

bluelotus Contributor

Jenn 2005, you should PM laurel and not post your email address, since it is now accessible to whoever reads this....just an idea. Good luck with finding a doctor.

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. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    2. - knitty kitty replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    3. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    4. - Scott Adams replied to Russ H's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      KAN-101 Treatment for Coeliac Disease

    5. - Scott Adams replied to miguel54b's topic in Related Issues & Disorders
      1

      Body dysmorphia experience


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,154
    • Most Online (within 30 mins)
      7,748

    bobadigilatis
    Newest Member
    bobadigilatis
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • trents
      This article does not address migraines at all.  Yes, red wine and sulfites are often mentioned in connection with migraine triggers. With me, any kind of alcoholic beverage in very modest amounts will reliably produce a migraine. Nitrous oxide generators, which are vaso dialators, also will give me migraines reliably. So, I think most of my migraines are tied to fluctuations vascular tension and blood flow to the brain. That's why the sumatriptan works so well. It is a vaso constrictor. 
    • knitty kitty
      Excessive dietary tyrosine can cause problems.  Everything in moderation.   Sulfites can also trigger migraines. Sulfites are found in fermented, pickled and aged foods, like cheese.  Sulfites cause a high histamine release.  High histamine levels are found in migraine.  Following a low histamine diet like the low histamine Autoimmune Protocol diet, a Paleo diet, helps immensely.    Sulfites and other migraine trigger foods can cause changes in the gut microbiome.  These bad bacteria can increase the incidence of migraines, increasing histamine and inflammation leading to increased gut permeability (leaky gut), SIBO, and higher systemic inflammation.   A Ketogenic diet can reduce the incidence of migraine.  A Paleo diet like the AIP diet, that restricts carbohydrates (like from starchy vegetables) becomes a ketogenic diet.  This diet also changes the microbiome, eliminating the bad bacteria and SIBO that cause an increase in histamine, inflammation and migraine.  Fewer bad bacteria reduces inflammation, lowers migraine frequency, and improves leaky gut. Since I started following the low histamine ketogenic AIP paleo diet, I rarely get migraine.  Yes, I do eat carbs occasionally now, rice or potato, but still no migraines.  Feed your body right, feed your intestinal bacteria right, you'll feel better.  Good intestinal bacteria actually make your mental health better, too.  I had to decide to change my diet drastically in order to feel better all the time, not just to satisfy my taste buds.  I chose to eat so I would feel better all the time.  I do like dark chocolate (a migraine trigger), but now I can indulge occasionally without a migraine after.   Microbiota alterations are related to migraine food triggers and inflammatory markers in chronic migraine patients with medication overuse headache https://pmc.ncbi.nlm.nih.gov/articles/PMC11546420/  
    • trents
      Then we would need to cut out all meat and fish as they are richer sources of tyrosine than nuts and cheese. Something else about certain tyrosine rich foods must be the actual culprit. 
    • Scott Adams
      I agree that KAN-101 looks promising, and hope the fast track is approved. From our article below: "KAN-101 shows promise as an immune tolerance therapy aiming to retrain the immune system, potentially allowing safe gluten exposure in the future, but more clinical data is needed to confirm long-term effects."  
    • Scott Adams
      Thank you so much for having the courage to share this incredibly vivid and personal experience; it's a powerful reminder of how physical ailments can disrupt our fundamental sense of self. What you're describing sounds less like a purely psychological body dysmorphia and more like a distinct neurological event, likely triggered by the immense physical stress and inflammation that uncontrolled celiac disease can inflict on the entire body, including the nervous system. It makes complete sense that the specific sensory input—the pressure points of your elbows on your knees—created a temporary, distorted body map in your brain, and the fact that it ceased once you adopted a gluten-free diet is a crucial detail. Your intuition to document this is absolutely right; it's not "crazy" but rather a significant anecdotal data point that underscores the mysterious and far-reaching ways gluten can affect individuals. Your theory about sensory triggers from the feet for others is also a thoughtful insight, and sharing this story could indeed be validating for others who have had similar, unexplainable sensory disturbances, helping them feel less alone in their journey.
×
×
  • 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.